LGI proteins in the nervous system

ASN NEURO 5(3):art:e00115.doi:10.1042/AN20120095 REVIEW ARTICLE OPEN ACCESS LGI proteins in the nervous system Linde Kegel*, Eerik Aunin*, Dies Meijer*1 and John R. Bermingham, Jr†1,2 *Department of Genetics and Cell Biology, Erasmus University Medical Center, PO Box 2040, 3000 CA Rotterdam, The Netherlands †McLaughlin Research Institute, 1520 23rd Street South, Great Falls, MT 59405, U.S.A. Cite this article as: Kegel L, Aunin E, Meijer D and Bermingham, Jr, JR (2013) LGI proteins in the nervous system. ASN NEURO 5(3):art:e00115.doi:10.1042/AN20120095 ABSTRACT The development and function of the vertebrate nervous system depend on specific interactions between different cell types. Two examples of such interactions are synaptic transmission and myelination. LGI1-4 (leucine-rich glioma inactivated proteins) play important roles in these processes. They are secreted proteins consisting of an LRR (leucinerich repeat) domain and a so-called epilepsy-associated or EPTP (epitempin) domain. Both domains are thought to function in protein–protein interactions. The first LGI gene to be identified, LGI1, was found at a chromosomal translocation breakpoint in a glioma cell line. It was subsequently found mutated in ADLTE (autosomal dominant lateral temporal (lobe) epilepsy) also referred to as ADPEAF (autosomal dominant partial epilepsy with auditory features). LGI1 protein appears to act at synapses and antibodies against LGI1 may cause the autoimmune disorder limbic encephalitis. A similar function in synaptic remodelling has been suggested for LGI2, which is mutated in canine Benign Familial Juvenile Epilepsy. LGI4 is required for proliferation of glia in the peripheral nervous system and binds to a neuronal receptor, ADAM22, to foster ensheathment and myelination of axons by Schwann cells. Thus, LGI proteins play crucial roles in nervous system development and function and their study is highly important, both to understand their biological functions and for their therapeutic potential. Here, we review our current knowledge about this important family of proteins, and the progress made towards understanding their functions. Key words: autosomal dominant lateral temporal (lobe) epilepsy (ADLTE), autosomal dominant partial epilepsy with auditory features (ADPEAF), epitempin, leucine-rich gliomainactivated protein, leucine-rich repeat (LRR), PNS development, synapse. CELL–CELL INTERACTIONS IN NERVOUS SYSTEM DEVELOPMENT Synapse formation and maturation require multiple interactions between presynaptic and postsynaptic neurons that are mediated by a diverse set of synaptic proteins (Han and Kim, 2008; McMahon and Diaz, 2011; Siddiqui and Craig, 2011). Initial synapse formation needs both the binding of secreted proteins to presynaptic and postsynaptic receptors, and the direct binding between presynaptic and postsynaptic transmembrane proteins. Many synaptogenic proteins have been described, some of which, like the secreted LGI proteins discussed here, are specific to vertebrates. Myelination also requires cell–cell interactions; myelin is required for rapid axonal transmission of electrical signals in the vertebrate nervous system. It consists of multiple wraps of membrane that permit saltatory conduction between specialized structures, the nodes of Ranvier. Myelination requires reciprocal interactions between the axon and oligodendrocytes in the CNS (central nervous system) or Schwann cells in the PNS (peripheral nervous system); reviewed in (Nave, 2010; Piaton et al., 2010; Quintes et al., 2010). As described below, LGI4 participates in axon-Schwann cell communication; it is crucial for PNS (but not CNS) myelination. In addition to synaptogenesis and myelination, LGI proteins are likely to participate in other cell–cell interactions as well. The study of this interesting family of proteins is critical for understanding proper development and function of the vertebrate nervous system, and for gaining insights into therapies for diseases that affect them. IDENTIFICATION OF THE LGI FAMILY As suggested by its name, leucine-rich glioma inactivated, the LGI protein family was discovered in gliomas. Loss of one copy rrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrrr 1 Correspondence may be addressed to either of these authors (email jbermingham@genetics.wustl.edu, jrbjr@po.mri.montana.edu or d.meijer@erasmusmc.nl). Sabbatical address: Department of Genetics, Campus Box 8232, Washington University School of Medicine, 660 S. Euclid Avenue, St. Louis, MO 63110-1093, U.S.A. Abbreviations: ADLTE, autosomal dominant lateral temporal (lobe) epilepsy; ADPEAF, autosomal dominant partial epilepsy with auditory feature; Akt, protein kinase B; AMPA, α-amino-3-hydroxy-5-methylisoxazole-4-propionic acid; CNS, central nervous system; EPTP, epitempin; GFP, green fluorescent protein; mEPSCs, miniature excitatory postsynaptic currents; LE, limbic encephalitis; LGI, leucine-rich glioma inactivated; LRR, leucine-rich repeat; LRR-CT, carboxyl-terminal portion of the LRR; NMDA, N-methyl-D-aspartate; Nrg1, neuregulin; PNS, peripheral nervous system; PTZ, pentylenetetrazole; VGKC, voltage-gated potassium channel.  C 2013 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. 2 asnneuro.org / Volume 5 (3) / art:e00115 167 L. Kegel and others of chromosome 10 is a common event in high-grade gliomas. In a search for genes that are mutated in these gliomas, Cowell and colleagues identified a gene in the 10q24 region that was rearranged as a result of a t(10;19)(q24;q13) balanced translocation in a T98G glioblastoma multiforme cell line (Chernova et al., 1998). They suggested that the complete loss of this gene, which contains four LRRs (leucine-rich repeats), contributes to the malignant progression of glial tumours. A completely independent line of inquiry implicated LGI1 in epilepsy. Epilepsy is a heterogeneous disease, and families with multiple epileptic individuals are important resources for identifying susceptibility genes. In one such family multiple individuals presented with partial seizures with auditory features, thereby permitting a susceptibility gene to be mapped to a 10-centimorgan region of chromosome 10 (Ottman et al., 1995). This type of epilepsy was named ADPEAF (autosomal dominant partial epilepsy with auditory features) (Winawer et al., 2000), and additional families with similar symptoms confirmed linkage to the same region of chromosome 10 (Winawer et al., 2002). Independently, a large five-generation Basque family with similar dominant partial epilepsy also demonstrated linkage to chromosome 10q (Poza et al., 1999). This inherited epilepsy was named ADLTE [autosomal dominant lateral temporal (lobe) epilepsy]. Making the assumption that the same gene was mutated in these two families reduced the chromosomal region containing the epilepsy gene to a 4.2 Mb sequence. All genes within this region were sequenced in three affected individuals of three different families revealing distinct mutations in the LGI1 gene. Extending the analysis to two additional families revealed two more mutations (Kalachikov et al., 2002). Independently, Morante-Redolat et al. (2002) identified mutations in the LGI1 gene in two families. Since these initial publications many more mutations in the LGI1 gene have been found in ADLTE/ADPEAF patients and the total number is now 33 (see Ho et al., 2012). The terms ADLTE and ADPEAF refer to the same clinical entity (OMIM 600512). In this review, we use the nomenclature of Winawer et al. (2000) and refer to the disease as ADPEAF. As we discuss here, LGI1 is associated with synapses in the nervous system and most recent research has focused on the role of LGI1 in nervous system function and disease. The other three LGI family members, LGI2–3 and -4, were cloned following in silico identification of LGI1-homologous genes in vertebrate genomes (Gu et al., 2002). Subsequently, mutations in Lgi2 and Lgi4 demonstrated that these genes perform important functions in the central and peripheral nervous systems. EVOLUTION OF LGI GENES LGI genes appeared in chordates [Branchiostoma floridae (amphioxus) has one LGI gene] and are found in all vertebrate 168  C genomes that have been examined to date. Early vertebrate genomes underwent two rounds of whole genome duplication (Ohno, 1970; Dehal and Boore, 2005) and presumably a single primordial LGI gene gave rise to four LGI genes. A third whole genome duplication occurred in the teleost fish lineage after the tetrapod-teleost split (Gillis et al., 2009; Van de Peer et al., 2009; Manning and Scheeff, 2010). The zebrafish, Danio rerio, a teleost, possesses two copies of lgi1 (lgi1a and lgi1b), two copies of lgi2 (lgi2a and lgi2b), a single copy of lgi3 and no copy of lgi4 (Gu et al., 2005b). A similar picture – with duplicated lgi1 and lgi2 genes, a single lgi3 gene and no lgi4 gene – emerges from the genomes of other teleost fishes such as cod, stickleback and platyfish (see the webpage of Ensembl.org). Following whole genome duplication events, gene families often contract, as genes with redundant functions are lost (Manning and Scheeff, 2010). In the case of fishes, lgi4 may have been lost as one or more other LGI genes assumed its functions in peripheral nerve development. Alternatively, lgi4 diverged from an ancestral LGI gene specifically in the tetrapod lineage. Coelacanths (Latimeria sp.) are an order of fish that diverged from teleost fishes prior to their third genome duplication and are thus more closely related to the ancestors of the tetrapods. The coelacanth genome (Amemiya et al., 2013) contains single copies of lgi1, lgi2, and lgi3 genes, but not lgi4. Surprisingly, the recently sequenced Xenopus tropicalis genome (Hellsten et al., 2010) has been found to contain lgi1, lgi2 and lgi4, but not lgi3. Although it remains to be seen if the absence of individual LGI genes in coelacanth and frog genomes is real, the current genome sequence data support the appearance of Lgi4 in tetrapods. As more genomes are sequenced, the pattern of LGI gene evolution will become clearer. STRUCTURE OF LGI PROTEINS All LGI family members have a calculated molecular mass of approximately 60 kDa (Chernova et al., 1998) and contain a signal peptide that is cleaved off, an LRR domain containing four LRR repeats flanked by cysteine-rich sequences (Kobe and Kajava, 2001) and an EPTP domain consisting of seven EPTP repeats (Figure 1A) (Scheel et al., 2002; Staub et al., 2002). The EPTP repeats most likely fold into a so-called seven bladed β-propeller, a structure that resembles a slightly conical doughnut. Both the LRR domain and the β-propeller structure provide a scaffold for specific protein interactions and are found in a wide range of proteins with diverse physiological function (Buchanan and Gay, 1996; Paoli, 2001b), but only a handful of LGI protein binding partners have been identified (see below). Some of these proteins interact with all LGI proteins, whereas others bind more selectively (Özkaynak et al., 2010; Thomas et al., 2010) and (E. Aunin, unpublished work). These proteins will be discussed in the context of the individual LGI proteins to which they bind. 2013 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. LGI proteins Figure 1 Structural characteristics of the LGI protein family In (A), the general domain structure of the LGI protein family is depicted. All LGI proteins have an SP (signal peptide) that is cleaved off (arrow in A) and is not included in the putative protein structures shown in (B). The glycosylation site present in all LGI members is indicated in (A) with a branched line structure. The putative structures of the LRR domain and EPTP domain were predicted separately using the HHpred tool (http://toolkit.tuebingen.mpg.de/hhpred) and the WDR5 protein structure (PDB 2GNQA) as template. Structures were visualized using the Accelrys Discovery Studio visualizer. The structure is colour-coded from N-terminus (blue) to C-terminus (red) and corresponds with the colour code in (A). The colour-code graphically reveals the Velcro β-strand (blue) interacting with the last β-strand (red) of the seventh EPTP module to zip up the EPTP domain structure. How the LRR domain and the EPTP domain are oriented towards each other is unknown. The stippled black line does not represent any structural feature but is only intended to show the linkage between the two domains. The LGI proteins’ LRR domain is most homologous to Slit proteins (Krex et al., 2002). Slit proteins are large secreted proteins involved in axonal guidance and neuronal migration through interaction with their receptor Roundabout (Robo). The Slit proteins contain four LRR domains, D1–D4, and each domain is approximately 31–33 % homologous to the LGI LRR domain. A model of the LGI1 LRR domain (Leonardi et al., 2011), based on the structure of Slit LRRs, suggests that it consists of four 24 amino acid long LRRs. The intron–exon structure of LGI genes further corroborates this conjecture as the repeats are encoded by four 72 nt long exons (exon 2 to 5). The LRRs with the N- and C-terminal flanking sequences form a slightly curved structure with parallel β-strands forming the concave face of the domain (Figure 1B). As Slit proteins dimerize (Howitt et al., 2004), one hypothesized function of the LRR domain is dimerization. Indeed, LGI1 is secreted as an oligomer (Fukata et al., 2006) raising the possibility that the LGI proteins homo- or heterodimerize with other LGI proteins or possibly with other LRR-containing proteins. The EPTP domain comprises the C-terminal three/fifths of LGI proteins. The name Epitempin derives from the observation that this domain is found in two epilepsy-associated proteins, LGI1 and GPR98/VLGR/MASS, the latter a transmembrane protein mutated in human and mouse auditory epilepsy (Skradski et al., 2001; Nakayama et al., 2002;  C McMillan and White, 2004). This name is a bit misleading as LGI3 and -4, and the deafness-associated protein TSPEAR (Delmaghani et al., 2012), also contain EPTP repeats but have not yet been associated with epilepsy. Notably, mutations in the EPTP-encoding genes LGI1, GPR98 and TSPEAR all produce auditory symptoms, either noise-induced seizures or deafness. As mentioned, the EPTP repeats of LGI proteins likely form a seven bladed β-propeller domain (Scheel et al., 2002; Staub et al., 2002). The β-propeller domain consists of four to ten modules (the blades), and is found in a wide variety of proteins in both prokaryotes and eukaryotes (Fulop and Jones, 1999; Jawad and Paoli, 2002; Pons et al., 2003; Chaudhuri et al., 2008). Each β-propeller module consists of four antiparallel β-strands that form a sheet warped like a propeller blade (see Figure 1B). In the case of the EPTP domain, seven of these modules associate to form a disc with a conical central pore, and stabilized by hydrophobic interactions between the blades (see Figure 1B). Sites for interactions with other proteins reside on the outer surfaces, and for some β-propellers, the pore contains a substrate-binding site, but whether or not anything associates with the central pore of LGI proteins is unknown. Recently, in silico model(s) of the LGI1 EPTP domain have been published, based on the structure of the β-propeller protein WDR5 (Limviphuvadh et al., 2010; Leonardi et al., 2011). A notable feature of the WDR5 structure is that the seven 2013 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. 169 L. Kegel and others clusters of four β-strands, seen in the primary sequence, are out of register with the seven blades in the structure (reviewed in Fulop and Jones, 1999; Xu and Min, 2011). Accordingly, the register of β-strands in the in silico model of LGI1 structure proposed by Leonardi et al. (2011) is shifted by one β-strand relative to the boundaries of each EPTP repeat that were described initially (Scheel et al., 2002; Staub et al., 2002). A characteristic of β-propeller domains with six or more repeats is the presence of a ‘Velcro’ or ‘molecular clasp’, sequence that holds the circular structure closed (reviewed in Paoli, 2001a). These Velcro sequences consist of one or more β-strands contributed by one terminal repeat module that are integrated into the β-sheet formed by the repeat at the other end, permitting inter-β-strand interactions to pull the entire β-propeller closed, thereby stabilizing its circular structure. Leonardi and colleagues propose that for LGI1, the N-terminal EPTP β-strand resides at the outside of the C-terminal β-propeller, with the C-terminal β-strand nested inside it (Figure 1B). The Leonardi model provides a plausible explanation for the deleterious phenotype of the 1639insA mutation in one family of ADPEAF patients (Kalachikov et al., 2002), and the LGI2 truncation seen in BJFE dogs (Seppälä et al., 2011). These mutations replace or remove the 11 Cterminal amino acids of LGI1 or LGI2, respectively. Their absence may preclude formation of the first EPTP domain, and preclude folding of the entire β-propeller structure. How the LRR and EPTP domains of LGI proteins are oriented relative to one another is not known. Currently, this important question cannot be answered by modelling alone. The crystal structure of an intact LGI protein is needed to provide insight into the specific functions of the four LGI proteins, and to provide better understanding of the effects of the different human LGI1 mutations. POST-TRANSLATIONAL MODIFICATION AND SECRETION OF LGI PROTEINS All LGI proteins possess consensus N-linked glycosylation sites (Figure 1A). Asn192 , located within the LRR-CT (C-terminal portion of the LRR) domain, resides in a glycosylation site that is conserved among all LGI members (Figure 1). Asn277 is part of a glycosylation site in some LGI1 and LGI2 orthologues, and a glycosylation site that includes Asn422 is found only in mammalian LGI1 proteins. These sites have been demonstrated to be glycosylated in LGI1 (Sirerol-Piquer et al., 2006). A triple glycosylation mutant of LGI1 is not secreted and secretion of the N192Q mutant is severely diminished, underscoring the importance of these glycosylation sites for normal maturation and secretion of LGI1. LGI4 is glycosylated at the LRR-CT site (Bermingham et al., 2006), but the functional significance of this is unknown. Based on the observations with LGI1, it is reasonable to postulate that LGI proteins require glycosylation for one or more steps in their secretion. 170  C Most ADPEAF mutations inhibit LGI1 secretion (de Bellescize et al., 2009; Di Bonaventura et al., 2011; Striano et al., 2011); see Table 1 in (Nobile et al., 2009). Many of these appear to alter the ability of the LRR domain or the EPTP domain to fold properly, thereby inhibiting their secretion. Accordingly, these mutations have provided limited information about the functional interactions of LGI1 protein. However, one ADPEAF mutation, Arg407 Cys is secreted normally (Striano et al., 2011). Rather than affecting LGI1 protein stability or secretion, this mutation may alter a functionally significant interaction domain for LGI1, and provides a proof of principle for utilizing LGI1 structural information to design mutations that will inform us about LGI1 function. LGI1 MUTATIONS IN ADPEAF As mentioned earlier, LGI1 mutations result in ADPEAF (OMIM 600512) (Kalachikov et al., 2002). ADPEAF patients present with complex partial and secondarily generalized seizures that are often associated with auditory auras (Nobile et al., 2009; Michelucci et al., 2013). The average age of seizure onset is in early adulthood (Winawer et al., 2000) and subtle abnormalities have been observed by magnetic resonance imaging from ADPEAF patients (Kobayashi et al., 2003; Tessa et al., 2007). This suggests that ADPEAF results from defects in brain development, which is consistent with the hypothesized functions for LGI1. ADPEAF mutations have begun to be examined in the context of other neurological diseases. LGI1 mutations do not appear to affect depression independently of epilepsy (Heiman et al., 2010). The LGI1 mutation in one ADPEAF family has been correlated with hyperactivity (Berghuis et al., 2013), and it will be important to determine if LGI1 mutations impact other diseases of synaptic connectivity. To date, 33 mutations at 29 distinct locations have been identified in LGI1 with an average penetrance of approximately 67 % (Rosanoff and Ottman, 2008; Nobile et al., 2009; Kawamata et al., 2010; Michelucci et al., 2013) (Figure 2). Not all ADPEAF patients possess mutations in LGI1; the penetrance of ADPEAF in families that segregate LGI1 mutations is higher than in ADPEAF families without LGI1 mutations (Michelucci et al., 2013), suggesting that the disease has a complex and heterogeneous pattern of inheritance. The dominant LGI1 mutations in ADPEAF could be either haploinsufficient (one wild-type copy makes insufficient amounts of protein for proper function) or dominant negative (i.e. mutant LGI1 interferes with wild-type LGI1 or its binding partners). The incomplete penetrance of many ADPEAF mutations, and the instability and/or inability to be secreted of many LGI1 proteins resulting from them suggests that these mutations are haploinsufficient (Senechal et al., 2005; Sirerol-Piquer, 2006). However, the observation that LGI proteins multimerize (Fukata et al., 2006) suggests a potential for some LGI1 mutations to exert dominant negative effects. Futhermore, overexpression of a truncated 2013 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. LGI proteins Figure 2  C A schematic diagram of human LGI1 protein In this ‘exploded’ view of LGI1, the individual LRR and EPTP modules are separated from one another; dashed lines connect amino acids that are linked in the intact protein. Amino acids are represented as filled, shaded or open circles, depending on their level of conservation. The bottom half of circles for amino acids that are changed by point mutations are coloured orange; all of these mutations are from human except for the mutation at Leu385 , which is from rat. For simplicity, frameshift mutations are omitted, with the exception of one at the C-terminus that provides evidence that the ‘Velcro’ model of β-propeller closure, in which the N-terminal β-strand is included in the seventh EPTP propeller fold. Human LGI1 mutations were obtained from (de Bellescize et al., 2009; Nobile et al., 2009; Di Bonaventura et al., 2011; Ho et al., 2012) and the rat mutation from (Baulac et al., 2012). For the EPTP domain, the β-propeller blades, which in large part would intersect the plane of the figure in the intact protein, have been laid flat. β-strands are outlined by yellow arrows (Leonardi et al., 2011). Disulfide bonds are depicted as solid lines, and glycosylation sites have a branched line structure. Boundaries of the eight LGI1 exons are presented as lines through the sequence, with the relevant exon numbers juxtaposed. Every 100th amino acid is labelled. 2013 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. 171 L. Kegel and others Table 1 Potential binding partners of Lgi proteins Proteins whose association with LGI proteins have been tested directly by co-immunoprecipitation or by co-localization of tagged proteins in cultured cells, are shown. References are abbreviated as follows: F06 (Fukata et al., 2006); F10 (Fukata et al., 2010); K (Kim et al., 2012); N (Nishino et al., 2010); Ok (Okabayashi and Kimura, 2010); Oz (Özkaynak et al., 2010); P (Park et al., 2008); Sa08 (Sagane et al., 2008); Sa10 (Sagane et al., 2010); Sp (Seppälä et al., 2011); T (Thomas et al., 2010); W (Owuor et al., 2009). In addition, LGI1 has been shown not to bind to ADAM12 (W), ROBO2 (F06), Stargazin (F06), NGR2(T), NGR3(T), and Kv1.1(F10). ADAM9 does not bind to LGI1 (F06, F10) or to LGI4 (N). Binding partner Lgi1 Lgi2 Lgi3 Lgi4 ADAM11 Weak (Sa08) Binds (Oz) Does not bind (Oz) Moderate (Sa08) Moderate (Sa08) Does not bind (Oz) Binds (Oz) Strong (Sa08, Sa10) Binds (T, W, F06; F10) Binds (Sp) Does not bind (F10) Binds (Oz, N) Strong (Sa08) Does not bind (Oz) Binds (O) Strong (Sa08) Binds (T, W, F06, F10) Binds (Sp) Binds (K) Binds (Oz, N) FLOTILLIN1 ND ND Binds (Ok) ND SYNTAXIN1 ND ND Binds (P) ND NGR1 Binds (T) ND ND ND Binds (W, F10) ADAM22 ADAM23 Binds (Oz, N) LGI1 (835delC, which corresponds to a truncation of the Cterminus of the LRR-CT and the entire EPTP domain) inhibited dendritic pruning in vivo, suggesting that this ADPEAF mutation has a dominant negative effect (Zhou et al., 2009). Some of the potential dominant negative effects may be attributable to endoplasmic reticulum stress and activation of the unfolded protein response, similar to what has been observed elsewhere (D’Antonio et al., 2013; Li et al., 2013; Roussel et al., 2013). Curiously, LGI1 was identified in a screen for genes with monoallelic expression (Wang et al., 2010), suggesting that such expression may explain the incomplete penetrance of some ADPEAF mutations, or the haploinsufficiency of others. Multiple mechanisms may produce the dominant phenotype of LGI1 mutations. LGI1 PROTEIN INTERACTIONS IN THE CNS All LGIs seem to interact with select members of the ADAM (A Disintegrin And Metalloprotease) transmembrane protein family (Table 1). More than 40 ADAMs have been identified in species from Caenorhabditis elegans to human. Some members are catalytically active metalloproteases and control cell signalling by activating membrane-bound growth factors or by shedding the ectodomain of cell-surface receptors (Seals and Courtneidge, 2003; Blobel, 2005). Other members are inactive and are thought to be involved in protein interactions, especially with integrins (D’Abaco et al., 2006). LGI1 binds to the extracellular domain of ADAM22, which binds to the third PDZ domain of PSD-95 through its cytoplasmic C-terminal ETSI-motif (Fukata et al., 2006). The first two PDZ domains of PSD-95 in turn bind to the C-terminal tail of stargazin, a transmembrane regulatory subunit of AMPA (α-amino-3hydroxy-5-methylisoxazole-4-propionic acid)-receptors that is critical for AMPA-receptor trafficking and gating (Chen et al., 2000; Tomita et al., 2005; Nicoll et al., 2006; Yokoi 172  C et al., 2012). In addition to the stargazin/AMPA receptor complex, Fukata’s group found that PSD-95 strongly associated with LGI1 and ADAM22 in rat brain (Fukata et al., 2006). Thus, PSD-95 may tether two protein complexes, stargazin/AMPAR and ADAM22/LGI1 (Figure 3A). Since PSD95 together with stargazin controls the number of AMPA receptors at synapses, this association could explain the increase of synaptic AMPA/NMDA (N-methyl-D-aspartate) ratio in hippocampal slices after incubation with LGI1; it suggests that LGI1 is an extracellular factor-controlling synaptic strength at excitatory synapses (Fukata et al., 2006). Additionally, interaction between ADAM23 and LGI1 has been identified in the brain (Fukata et al., 2010) and on cultured neurons (Owuor et al., 2009). Both ADAM22 knockout and ADAM23 knockout mice show strong overlap in phenotype with LGI1 knockout mice, which is characterized by severe spontaneous epilepsy and premature death (Sagane et al., 2005; Owuor et al., 2009; Chabrol et al., 2010; Fukata et al., 2010; Yu et al., 2010). Additionally, a point mutation in Adam23 has been found in epileptic Belgian Shepherd dogs (Seppälä et al., 2012). Importantly, ADAM22 and ADAM23 co-assemble in the brain dependent on LGI1 (Fukata et al., 2010). Thus, it was hypothesized that LGI1 forms a bridge between presynaptic ADAM23 and postsynaptic ADAM22 (Fukata et al., 2010) (Figure 3) effectively regulating trans-synaptic interactions contributing to synaptic strength. In addition to ADAM22 and ADAM23, LGI1 also binds to ADAM11 (Sagane et al., 2008), which is an ADAM protein essential for spatial learning, motor coordination and nociceptive responses (Takahashi et al., 2006a, 2006b). However, the question whether ADAM11 resides within the same complex with LGI1, ADAM22 and ADAM23 was not addressed and electro-physiological studies will be needed to determine if ADAM11 has a role in synaptic transmission and plasticity. Furthermore, the interaction between ADAM23 and LGI1 affects neurite outgrowth. This conclusion is based on the observation that addition of LGI1 to DRGs or hippocampal neurons causes a dose dependent increase in neurite 2013 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. LGI proteins Figure 3 Possible mechanisms by which LGI proteins participate in cell–cell interactions Panels (A–C) depict several possible mechanisms by which LGI1 controls synapse development and function, and LGI4 controls PNS development. Note that these mechanisms are not mutually exclusive; the figure simply summarizes what currently is known or postulated for each interaction. (A) At synapses, LGI1 dimers may form a bridge between post-synaptic ADAM22, which is linked to the stargazin/AMPAR complex through PSD95 and stargazin, and presynaptic ADAM23 (Fukata et al., 2010). LGI1 has an effect on Kv1.1 inactivation through mechanisms that are unclear (Fukata et al., 2006). (B) In peripheral glial precursors, LGI4 appears to act as a paracrine or autocrine factor through binding to ADAM22 (Nishino et al., 2010). (C) During Schwann cell ensheathment and myelination of axons, LGI4 binds to the disintegrin domain of ADAM22. This interaction could trigger signalling or protein localization within the axon, thereby activating signal(s) to the Schwann cell. An LGI4–ADAM22–PSD95 interaction could cluster proteins at the axonal membrane. Alternatively, LGI4 binding to ADAM22 could induce the formation of protein complex(es) extracellularly. LGI4 might modulate ADAM22–integrin interactions, which also utilize the ADAM22 disintegrin domain (D’Abaco et al., 2006). outgrowth, and this effect is reduced for neurons cultured from Adam23 knockout mice (Owuor et al., 2009). LGI1 protein appears to affect NMDA-receptor subunit expression. The NMDA receptor (NMDA-R) forms a heterotetramer between two NR1 and two NR2 subunits. A hallmark of glutamatergic synapse maturation is the change in postsynaptic NMDA-R NR2 subunit composition (Barth and Malenka, 2001; Waites et al., 2005). The NR2B subunit is mainly expressed in immature neurons of the early postnatal brain. During development, the number of NR2A subunits grows, and eventually NR2A subunits outnumber NR2B subunits. LGI1 expression in vivo increases when the NR2B/NR2A ratio decreases, and when mutant ADPEAF LGI1 is overexpressed in mice, NR2B/NR2A increases (Zhou et al., 2009). These observations suggest that LGI1 regulates postsynaptic function during development. The same study showed that overexpressed ADPEAF mutant LGI1 blocks the normal developmental pruning of excess neuronal dendrites, resulting in an increase of excitatory synaptic transmission and seizure susceptibility. Both LGI1 and integrins (Chavis and Westbrook, 2001) seem to be crucial to the synchronous maturation of pre- and postsynaptic membrane functions of glutamatergic synapses during postnatal development and both bind the same disintegrin domain of ADAM proteins (Fukata et al., 2006; Yang et al., 2006). Furthermore, both integrin and LGI1 regulate NR2 subunit composition via tyrosine kinase  C signalling (Chavis and Westbrook, 2001; Zhou et al., 2009). These observations suggest that LGI1, integrins and ADAM proteins may cooperate to promote glutamatergic synapse maturation. LGI1 also indirectly binds Kv1.1 VGKC (voltage-gated potassium channels), which is a major constituent of presynaptic A-type channels that modulate synaptic transmission in CNS neurons (Schulte et al., 2006). LGI1 protein expression was reported to reduce Kv1.1 inactivation via the intracellular β-subunit of the channel (Schulte et al., 2006). However, since LGI1 has a signalling sequence and is secreted, it is unlikely that LGI1 competes with Kvβ1 for binding to Kv1.1. In contrast to wild-type LGI1 protein, certain mutant LGI proteins that cause ADPEAF in patients could not reduce Kv1.1 inactivation (Schulte et al., 2006). Interestingly, these same mutant LGI proteins are not secreted (Senechal et al., 2005; Sirerol-Piquer et al., 2006; Nobile et al., 2009) suggesting that LGI1 needs to be secreted prior to having an effect on channel inactivation. Since the LRR domains of LGI proteins are very homologous to the Slit proteins, they might have similar functions. Indeed, LGI1 counteracts myelin-induced growth cone collapse and neurite outgrowth inhibition (Thomas et al., 2010). LGI1 binds to Nogo receptor 1 (NgR1), raising the possibility that LGI1 is an antagonist of myelin-based growth inhibitors (Thomas et al., 2010). ADAM22 resides in a complex with 2013 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. 173 L. Kegel and others NgR1 and facilitates LGI1 binding to this receptor, suggesting that NgR1 and ADAM22 collaborate to create an LGI1 binding complex that is important for synapse formation (Thomas et al., 2010). It has not been tested whether other LGI proteins bind any of the Nogo receptors. Together these observations underscore an important role for LGI1 in brain excitation and development, explaining why LGI1 mutations result in epilepsy. THE ROLE OF LGI1 IN CNS DEVELOPMENT AND FUNCTION In the CNS, LGI1 expression patterns are complex. Although the LGI1 gene is active in the caudal ganglionic eminence at e13.5 in the mouse (Kusuzawa et al., 2012), it appears to be expressed primarily postnatally. It is expressed in multiple, discrete locations in adult brain (Kalachikov et al., 2002; Morante-Redolat et al., 2002; Senechal et al., 2005; Magdaleno et al., 2006; Ribeiro et al., 2008; Yu et al., 2010). Studies using transgenic mice that possess a bacterial artificial chromosome in which Lgi1 regulatory sequences drive expression of GFP (green fluorescent protein) have produced similar results (Head et al., 2007). In these mice, Lgi1-driven GFP expression is observed in glial cells in some brain regions, whereas in others, GFP expression was exclusively neuronal. The observation of Lgi1-driven GFP expression in glial cells of the midbrain and elsewhere is significant in light of the role of the midbrain in the propagation of audiogenic seizures (Garcia-Cairasco et al., 1993; Garcia-Cairasco, 2002; Doretto et al., 2009). The importance for normal CNS function of LGI1 expression in specific cell types and brain regions remains to be determined. Mice and rats that lack Lgi1 die of seizures during the third postnatal week, showing that normal development or function of the CNS requires LGI1 (Chabrol et al., 2010; Fukata et al., 2010; Yu et al., 2010; Baulac et al., 2012). Two of the three independently created lines of Lgi1 knockout mice have been subjected to electrophysiological analyses. mEPSCs (miniature excitatory postsynaptic currents) result from the spontaneous release of synaptic vesicles in the absence of a stimulus; changes in their frequency suggest a presynaptic defect, whereas changes in their amplitude suggest a postsynaptic defect. In brain slices from their Lgi1 mutant mice, Fukata et al. (2010) found a decrease in mEPSC amplitude but no change in frequency, suggesting that LGI1 functions postsynaptically. In contrast, Yu et al. (2010) observed an increase in the frequency of mEPSCs with no differences in their amplitudes using brain slices from their Lgi1 knockout mice. Thus, despite the similar seizure phenotypes of their mouse strains, the groups came to opposite conclusions as to whether LGI1 acts pre- or postsynaptically. Other electrophysiological studies on BAC transgenic mice overexpressing either wild-type Lgi1 or a mutant form that is found in AD- 174  C PEAF, suggest that LGI1 acts both pre- and postsynaptically (Zhou et al., 2009). The apparent paradox may result from subtle differences in complicated experimental procedures, or more interestingly, it might reflect different activities that occur in vivo. Mice expressing mutant LGI1 also display reduced developmental pruning of dendritic arbors of hippocampal granule cells and increased spine density, thereby increasing neural excitability (Zhou et al., 2009). Similarly, it was demonstrated recently that LGI1 also regulates the pruning of retinogeniculate fibres (Zhou et al., 2012). These observations are consistent with increased neuronal outgrowth of wild-type mouse neurons by Lgi1 (Owuor et al., 2009). Thus, LGI–ADAM complexes add to a growing list of trans-synaptic complexes whose precise role in synaptic maturation and preservation are yet to be elucidated (reviewed in McMahon and Diaz, 2011; Siddiqui and Craig, 2011). Lgi1 MUTATIONS IN ZEBRAFISH AND RATS Rats and zebrafish with mutations in their LGI1 homologues are important resources for the development of new treatments for ADPEAF and perhaps other epilepsies as well. Expression of both homologues of LGI1 in zebrafish, lgi1a and lgi1b, has been knocked down using antisense morpholinos, demonstrating that the two genes have acquired distinct but overlapping developmental functions (Teng et al., 2010, 2011). Low-level inhibition of lgi1a has no effect on fish morphology, but sensitizes them to the seizure-inducing drug PTZ (pentylenetetrazole). High-level inhibition of lgi1a produces developmental abnormalities, including reductions in brain, eyes and tail, presumably due to increased CNS apoptosis; these fish also display seizure-like hyperactive swimming behaviours (Teng et al., 2010). In contrast, lgi1b knockdown fish display hydrocephalus and heart oedema, but not hyperactivity, yet retain sensitivity to PTZ (Teng et al., 2011). Rats that carry an ENU (N-ethyl-N-nitrosourea)-generated leucine to arginine mutation (L385R) in the fourth EPTP domain of LGI1 recapitulate the susceptibility to audiogenic seizures seen in ADPEAF, and display a similar profile of anti-epileptic drugs that suppress those seizures (Baulac et al., 2012). The Zebrafish lgi1 mutants will permit screens for small molecules that ameliorate their abnormal phenotypes, whereas the Lgi1 mutant rats will be useful for preclinical testing of candidate antiepileptic drugs. LGI1 IN GLIOMAS AND OTHER CANCERS Although LGI1 was identified initially from chromosomal breakpoint(s) in high-grade gliomas, and was proposed to 2013 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. LGI proteins function as a tumour suppressor gene (Chernova et al., 1998), its role in oncogenesis remains controversial. LGI1 expression is reduced or absent in many glioma cell lines (Chernova et al., 1998; Krex et al., 2002; Rossi et al., 2005); it also has been reported to be down-regulated in glioma tumours (Besleaga et al., 2003), in Barrett’s-related adenocarcinoma of the esophagus (Peng et al., 2008), and in prostate cancer (Cowell et al., 2010). LGI1 expression in neuroblastoma cells inhibits proliferation and causes apoptosis (Gabellini et al., 2006), further suggesting its anti-oncogenic potential. In glioma cells, LGI1 re-expression reduces their ability to proliferate and form colonies on soft agar in one study (Kunapuli et al., 2003), but not in another (Krex et al., 2002). In contrast, co-expression of a neuronal marker and LGI1 in gliomas suggests that LGI1 expression levels in these tumours may relate to the number of trapped neurons (Piepoli et al., 2006), and ADPEAF patients do not show increased frequencies of glioma (Brodtkorb et al., 2003; Gu et al., 2005a). An important use of Lgi1 knockout mice will be to assess their susceptibility to tumorigenesis. Additionally, the effect of LGI1 expression on increasing AKT (protein kinase B) signalling, reducing ERK (extracellular-signal-regulated kinase) signalling, and reducing matrix metalloproteinase expression in glioma and other cells in culture (Kunapuli et al., 2004; Sirerol-Piquer et al., 2006; Kunapuli et al., 2010) may provide clues about its function in vivo. LGI1 AND LIMBIC ENCEPHALITIS LE (limbic encephalitis) is a neurological autoimmune disease associated with antibodies against a variety of antigens (reviewed in Tuzun and Dalmau, 2007; Irani and Vincent, 2011; Vincent et al., 2011). Symptoms include memory loss, confusion, brain MRI abnormalities and seizures. Recently, in such patients auto-immune antibodies against LGI1 have been found (Irani et al., 2010; Lai et al., 2010). As the seizure susceptibility of LE patients is also observed in ADPEAF patients and Lgi1 mutant rats and mice, it is reasonable to assume that at least some of the LE symptoms result from a reduction in LGI1 levels. Initially, LE was considered rare and tumour-associated. Currently, it is recognized also in patients free of tumours, to present with a variety of symptoms, and to involve tissues beyond the limbic system. VGKCs are a common autoimmune antigen in these patients. AntiVGKC antibodies typically are detected by their ability to immunoprecipitate radio-labelled α-dendrotoxin, a potassium channel-binding protein, after it is added to lysates of brain tissue. However, upon further study, it was found that most of these antibodies reacted with LGI1 and not with potassium channel subunits (Irani et al., 2010; Lai et al., 2010). In fact, almost 90 % of these LE cases possess LGI1-reactive sera. Some cases of LE are preceded by (a prodrome) or overlap with faciobrachial dystonic seizures, which are character-  C ized by frequent brief seizures that typically affect an arm and ipsilateral face (Irani et al., 2011). Recognition of these clinical signs as a prelude to full LE provides a time window for early therapeutic intervention to limit the severity of LE symptoms and maybe prevent permanent disability. These clinical observations confirm that LGI1 is essential for proper functioning of vertebrate synapses, not only for their maturation. Epilepsy affects 1 % of people worldwide; many of these cases are idiopathic and may have an autoimmune aetiology. Therefore the low prevalence of ADPEAF may understate the importance of LGI1 as an epilepsy gene. Should pathogenic anti-LGI1 antibodies bind to specific epitopes, these epitopes could be druggable and lead to effective new epilepsy treatments. What can anti-LGI1-mediated LE tell us about LGI1 function? First, the onset of pathology in LE patients suggests that LGI1 is required for functioning of fully developed synapses, in addition to its role in synaptic maturation (Owuor et al., 2009). The differences between the symptoms of ADPEAF and LE patients may reflect disruption in both developing and mature synapses in the former, versus only mature synapses in the latter. Secondly, faciobrachial dystonia likely involves the basal ganglia (Irani et al., 2010; Plantone et al., 2013), suggesting that Lgi1 expression there (Head et al., 2007) is functionally significant. Thirdly, patient anti-LGI1 antibodies trigger epileptiform activity in hippocampal slices (Lalic et al., 2011). This experimental model system will help identify mechanisms by which LGI1 controls synaptic activity. Fourthly, LE patient LGI1 antibodies may disrupt specific LGI1 interactions with ADAM proteins or other accessory proteins. Characterization of these interactions will provide additional insights into synaptic function. Curiously, one patient’s serum was positive for LGI1 immunoreactivity, but negative in the immunoprecipitation assay for VGKCs, suggesting VGKCindependent functions for LGI1 (Irani et al., 2010). Thus, the identification of a connection between LGI1 and LE will advance both our understanding of synaptic biology, and our approach towards diagnosis and treatment of epilepsy. THE ROLE OF LGI2 IN CNS DEVELOPMENT LGI2 is associated with canine Benign Familial Juvenile Epilepsy. In the Italian water dog Lagotto Romagnolo, the disease is transient, generally disappearing by 10 weeks of age, and could serve as a model for human remitting epilepsies. Analysis of a Finnish pedigree of these dogs indicated a primarily recessive inheritance (Jokinen et al., 2007). Using an expanded pedigree of these dogs, Seppälä and colleagues identified 11 pairs of discordant siblings (one affected, one not). Their DNA was subjected to genome-wide association analysis, revealing a region of homozygosity on canine chromosome 3. Subsequent sequencing revealed that roughly 36 % of Lagatto Romagnolo dogs carry a point mutation 2013 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. 175 L. Kegel and others in LGI2 that results in truncation of 11 amino acids from the C-terminus of the mutant LGI2 protein (Seppälä et al., 2011), indicating that LGI2, like LGI1, is an epilepsy gene. Structurally, this mutation is adjacent to the frameshift mutation in LGI1 in ADPEAF patients described by Kalachikov and colleagues (Kalachikov et al., 2002), providing additional evidence for the requirement of the C-terminal amino acids of LGI proteins to hold the EPTP domain structure together, as predicted by the Velcro model of β-propeller folding. The protein interactions of LGI2 are less well studied than are those of LGI1. In culture, LGI2 was found to bind to the cell surface of ADAM11-expressing cells, but not to cells that expressed either ADAM22 or ADAM23 (Özkaynak et al., 2010). However, a later study in rat brain showed that LGI2 was, like LGI1, co-immunoprecipitated with both ADAM22 and ADAM23 antibodies, suggesting that LGI2 interacts – at least indirectly – with these ADAM proteins (Seppälä et al., 2011). As mentioned above, a truncating mutation in LGI2 causes benign juvenile epilepsy in dogs. Just like most mutations in LGI1 causes the mutated protein to be retained in the cell and degraded, this mutation of LGI2 completely abolishes its secretion (Seppälä et al., 2011). These observations suggest that LGI1 and LGI2 function through a similar mechanism that affects synaptic maturation at different time points of postnatal nervous system development. Importantly, LGI2 expression in the brain is highest preceding axonal pruning and before the onset of epilepsy, suggesting that LGI2 acts during the network construction phase (Seppälä et al., 2011). LGI1 might then act during the pruning phase to ensure an electrically stable network to serve the rest of the animal’s life, explaining why in LGI2-mutant dogs’ epileptic episodes are only seen in young animals. MULTIPLE POTENTIAL FUNCTIONS OF LGI3 Unlike Lgi1, Lgi2 and Lgi4, mutations in Lgi3 have yet to be associated with a pathological phenotype in humans or experimental animals. Mice in which Lgi3 exon1 (including the initiation codon) has been deleted appear normal (Kim et al., 2013), although a residual 75 kD isoform suggests the existence of an alternative start site (Park et al., 2008; Kim et al., 2013). In vitro experiments using cell lines suggests that LGI3 may perform several distinct functions. Putative LGI3-specific antibodies co-immunoprecipitate syntaxin1, but not SNAP25 or other components of the secretory apparatus (Park et al., 2008). Curiously, the C-terminus of syntaxin1 is buried within the plasma membrane, and is inaccessible (Suga et al., 2003). Therefore its interaction with LGI3 (a) occurs in the cytoplasm, (b) is indirect, perhaps mediated by ADAM proteins or (c) occurs as a result of tissue homogenization. The first two possibilities are reminiscent of the interaction between 176  C LGI1 and Kvβ1 (Schulte et al., 2006). Amyloid Aβ40 and Aβ42 peptides transiently up-regulate LGI3 expression in astrocytes, and LGI3 appears to promote Aβ endocytosis through an interaction with flotillin1 (Kimura et al., 2007; Okabayashi and Kimura, 2007, 2008, 2010). Thus LGI3 may mediate endocytosis for both syntaxin1 and amyloid peptides. LGI3 may also function in cell types other than astrocytes. LGI3 expression in brain increases postnatally and it is expressed in neurons but not in oligodendrocytes (Lee et al., 2006; Okabayashi and Kimura, 2007), but it is enriched in homogenates of CNS myelin relative to homogenates of whole brain (Dhaunchak et al., 2010). These observations suggest that it may function in myelinated nerve fibres. Additionally, LGI3 induces neurite outgrowth and increases phosphorylation of the signal transduction proteins Akt and FAK (focal adhesion kinase) (Park et al., 2010). Keratinocytes express LGI3, and it may promote their survival following UV irradiation (Lee et al., 2012). Multiple neural crest-derived cell types express Lgi3, including melanoma cell lines (Rossi et al., 2005), DRG neurons (Bermingham et al., 2006) and adipocytes (Kim et al., 2012). LGI3 suppresses expression of the adipocyte hormone adiponectin (Kim et al., 2013), and it attenuates preadipocyte differentiation through binding to Adam23 (Kim et al., 2012). It is at present unclear what common LGI3mediated mechanism might underlie these diverse biological functions. Together these observations suggest multiple functions for LGI3 that await further elucidation by the analysis of Lgi3 mutant mice. INVOLVEMENT OF LGI4 IN CELL–CELL INTERACTIONS IN THE PERIPHERAL NERVOUS SYSTEM Cell–cell interactions are required during PNS development for Schwann cell proliferation, migration, survival and myelination; however, the molecular mechanisms mediating these interactions are poorly understood. Study of the claw paw mutation in mice has revealed a novel LGI4-mediated signalling pathway that controls peripheral myelination. In 1977, Nelda Blaisdell, an animal technician handling C57BL/6-obese mice at The Jackson Laboratory in Bar Harbor, Maine, noted a litter in which two pups had limb abnormalities. Rather than holding their forelimbs up towards the head as most mouse pups do, they were held out, away from the body, or lowered towards the thorax. Mating of the littermates of these affected pups demonstrated that the phenotype was heritable. The new spontaneous mutation, called claw paw (clp) caused PNS hypomyelination without affecting central myelin (Henry et al., 1991). Because of the similarity in its myelination phenotype with that of mice lacking the POU domain transcription factor POU3f1/Oct6 (Bermingham et al., 1996; Jaegle et al., 1996), the clp 2013 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. LGI proteins mutation was investigated further. However, the clp mutation mapped to a separate locus on chromosome 7, and initial Oct6 expression was not affected (Darbas et al., 2004; Bermingham et al., 2006). The clp mutation was positionally cloned using a series of backcrosses, and found to result from an insertion in the Lgi4 gene (Bermingham et al., 2006), demonstrating a critical role for LGI4 in peripheral myelination. Claw paw (clp/clp) mice, in which LGI4 is not secreted (Bermingham et al., 2006), display a delay in radial sorting of axon fibres, and nerve-grafting experiments demonstrate that LGI4 function is required in Schwann cells and possibly in neurons (Darbas et al., 2004). LGI4 binds to ADAM22 (Table 1), and Adam22 knockout mice show a similar peripheral hypomyelination and forelimb phenotype to claw paw mice (Sagane et al., 2005; Nishino et al., 2010; Özkaynak et al., 2010); peripheral hypomyelination also is seen following Schwann cell-specific deletion of Lgi4, and neuron-specific deletion of Adam22 (Özkaynak et al., 2010). Thus, Schwann cell-secreted LGI4 appears to interact with ADAM22 on peripheral axons and in this way enable Schwann cell–neuron communication. The interaction could trigger a reciprocal ensheathment and/or myelination signal to Schwann cells (Figure 3). The nature of these putative signalling components is unknown. One possibility is that LGI4–ADAM22 modulates Nrg1 (neuregulin) signalling, but if so, it does not modulate the surface expression of Nrg1, a major regulator of Schwann cell migration and myelination (Özkaynak et al., 2010). Another possibility is that LGI4 modulates an already existing interaction between ADAM22 and another ADAM22-binding protein on the Schwann cell membrane, for example integrins (Figure 3). In addition to ADAM22, LGI4 can also bind to ADAM23 and ADAM11 (Sagane et al., 2008; Özkaynak et al., 2010). Whether these ADAM proteins play a role in PNS myelination is at present unknown. It is possible that – in analogy with the proposed role of LGI1 in regulating trans-synaptic adhesion (Figure 3) – LGI4 links axons and Schwann cells through interactions with ADAM22 in the axonal membrane and ADAM23 or ADAM11 in the Schwann cell membrane. Lgi4 is expressed initially by neural crest stem cells but its expression becomes restricted to the glial cells that derive from them. These neural crest-derived cells include, in addition to Schwann cells, enteric glial cells with properties resembling those of astrocytes in CNS, and satellite cells of (para-) sympathetic and dorsal root ganglia (reviewed in Jessen, 2004). Analysis of cultures derived from embryonic enteric and (para-) sympathetic ganglia revealed that LGI4 is required for proper levels of proliferation of glial precursors, but not for glial fate determination of neural crest stem cells (Nishino et al., 2010). Interestingly, embryonic sciatic nerve Schwann cells proliferated normally in the absence of LGI4 (Nishino et al., 2010), demonstrating that different types of PNS glial cells have different requirements for LGI4. Whether the proliferative effect of LGI4 on these glial precursors is mediated through an ADAM receptor is an important unanswered question. Thus, LGI4 has multiple  C functions including proliferation of enteric glia and satellite cells in PNS, and later, myelin formation in Schwann cells. The requirement for LGI4 for embryonic enteric glial cell and satellite cell proliferation contrasts with that of LGI1 for glioma cells as LGI1 inhibits proliferation of glioma cells (Chernova et al., 1998; Krex et al., 2002). CONCLUDING REMARKS Over the last decade, LGI proteins have emerged as important regulators of cellular interactions in the nervous system and their mutation has been associated with diverse pathologies such as epilepsy, psychiatric disorders and hypomyelination. However, their mechanism or mechanisms of action remain a mystery. Advances in understanding one LGI family member may inform us about the functions of others. LGI proteins are secreted proteins, but because most mutations in LGI proteins affect their secretion, these mutations do not tell us much about the mechanism of action of LGI proteins. The disease-associated mutation in LGI1 that appears to affect its interactions with other proteins rather than its secretion (Striano et al., 2011) suggests that identification of additional disease-associated, yet normally secreted, LGI mutant proteins will help map their functionally relevant interfaces. Further insight into LGI protein function may come from studies that map the epitopes within LGI1 recognized by sera of different LE patients. It is not known at present whether the sera from different LE patients recognize the same or different epitopes. Mapping of these epitopes might tell us how these antibodies interfere with normal LGI1 function and cause disease. The crystal structure of an LGI protein will inform us of its overall shape, and how its functionally significant interfaces are oriented. These studies will provide a fuller understanding of LGI protein interactions with other proteins. All LGI proteins appear to interact with ADAM22/23/11 receptors albeit probably with very different affinities. The high degree of identity among LGI proteins and their affinity for these ADAM receptors suggest that they act through a similar mechanism. However, it is not known whether the LGI proteins are functionally equivalent or serve distinct functions in different parts of the nervous system at different developmental stages. The one published experiment that addresses this issue demonstrated that LGI3 could not replace LGI1 in CNS synaptic development (Fukata et al., 2010), possibly due to a much lower affinity of LGI3 for the ADAM22 receptor. An understanding of the functional relationship of LGI proteins will require the determination of the relative affinities of these proteins for the ADAM receptors. Another open question is how LGI–ADAM interactions influence ADAM–integrin interactions: Are they mutually exclusive or does LGI binding potentiate ADAM–integrin interactions? Answering these questions, in addition to identifying the full 2013 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. 177 L. Kegel and others repertoire of LGI receptors in different parts of the nervous system will elucidate mechanistic aspects that are common to the LGI protein family as well as to those that are member specific. LGI proteins evolved with vertebrates, but many of the intercellular interactions in which they function, such as synapses between neurons, clearly predate them. Are the biological functions of LGI proteins required in invertebrates, and if so, what proteins perform them? If LGI proteins perform vertebrate-specific functions, could their appearance have been a crucial step in the evolution of complex vertebrate nervous systems? As we learn more about what LGI proteins do, the answers to these questions will become apparent. Importantly, we anticipate that ongoing and future clinical, genetic and biochemical work directed towards an understanding of the biology and pathology of LGI proteins will ultimately lead to novel approaches in combating the devastating neurological diseases associated with mutations in the LGI gene family. FUNDING Research in the laboratory of D.M. is supported by the Dutch government to the Netherlands Institute for Regenerative Medicine (NIRM) [grant number FES0908], VICI [grant number 918.66.616] and the European Union [grant number NGIDD FP7 HEALTH-F2-2008-201535]. J.R.B. has been supported by the National Institute for Neurological Disorders and Stroke [grant number R01NS40751] and by the McLaughlin Research Institute. REFERENCES Amemiya CT, Alföldi J, Lee AP, Fan S, Philippe H, Maccallum I, Braasch I, Manousaki T, Schneider I, Rohner N et al. (2013) The African coelacanth genome provides insights into tetrapod evolution. Nature 496:311–316. Barth AL, Malenka RC (2001) NMDAR EPSC kinetics do not regulate the critical period for LTP at thalamocortical synapses. Nat Neurosci 4:235–236. Baulac S, Ishida S, Mashimo T, Boillot M, Fumoto N, Kuwamura M, Ohno Y, Takizawa A, Aoto T, Ueda M, Ikeda A, LeGuern E, Takahashi R, Serikawa T (2012) A rat model for LGI1-related epilepsies. Human molecular genetics 21:3546–3557. Berghuis B, Brilstra EH, Lindhout D, Baulac S, de Haan GJ, van Kempen M (2013) Hyperactive behavior in a family with autosomal dominant lateral temporal lobe epilepsy caused by a mutation in the LGI1/epitempin gene. Epilepsy & behavior: E&B 28:41–46. Bermingham Jr, JR, Scherer SS, O’Connell S, Arroyo E, Kalla KA, Powell FL, Rosenfeld MG (1996) Tst-1/Oct-6/SCIP regulates a unique step in peripheral myelination and is required for normal respiration. Genes Dev 10:1751–1762. Bermingham Jr, JR, Shearin H, Pennington J, O’Moore J, Jaegle M, Driegen S, van Zon A, Darbas A, Özkaynak E, Ryu EJ, Milbrandt J, Meijer D (2006) The claw paw mutation reveals a role for Lgi4 in peripheral nerve development. Nat Neurosci 9:76–84. 178  C Besleaga R, Montesinos-Rongen M, Perez-Tur J, Siebert R, Deckert M (2003) Expression of the LGI1 gene product in astrocytic gliomas: downregulation with malignant progression. Virchows Arch 443:561–564. Blobel CP (2005) ADAMs: key components in EGFR signalling and development. Nat Rev Mol Cell Biol 6:32–43. Brodtkorb E, Nakken KO, Steinlein OK (2003) No evidence for a seriously increased malignancy risk in LGI1-caused epilepsy. Epilepsy Res 56:205–208. Buchanan SG, Gay NJ (1996) Structural and functional diversity in the leucine-rich repeat family of proteins. Prog Biophys Mol Biol 65:1–44. Chabrol E, Navarro V, Provenzano G, Cohen I, Dinocourt C, Rivaud-Pechoux S, Fricker D, Baulac M, Miles R, Leguern E, Baulac S (2010) Electroclinical characterization of epileptic seizures in leucine-rich, glioma-inactivated 1-deficient mice. Brain 133:2749–2762. Chaudhuri I, Soding J, Lupas AN (2008) Evolution of the beta-propeller fold. Proteins 71:795–803. Chavis P, Westbrook G (2001) Integrins mediate functional pre- and postsynaptic maturation at a hippocampal synapse. Nature 411:317–321. Chen L, Chetkovich DM, Petralia RS, Sweeney NT, Kawasaki Y, Wenthold RJ, Bredt DS, Nicoll RA (2000) Stargazin regulates synaptic targeting of AMPA receptors by two distinct mechanisms. Nature 408:936–943. Chernova OB, Somerville RP, Cowell JK (1998) A novel gene, LGI1, from 10q24 is rearranged and downregulated in malignant brain tumors. Oncogene 17:2873–2881. Cowell JK, Head K, Kunapuli P, Vaughan M, Karasik E, Foster B (2010) Inactivation of LGI1 expression accompanies early stage hyperplasia of prostate epithelium in the TRAMP murine model of prostate cancer. Exp Mol Pathol 88:77–81. D’Abaco GM, Ng K, Paradiso L, Godde NJ, Kaye A, Novak U (2006) ADAM22, expressed in normal brain but not in high-grade gliomas, inhibits cellular proliferation via the disintegrin domain. Neurosurgery 58:179–186, discussion 179-186. D’Antonio M, Musner N, Scapin C, Ungaro D, Del Carro U, Ron D, Feltri ML, Wrabetz L (2013) Resetting translational homeostasis restores myelination in Charcot-Marie-Tooth disease type 1B mice. J Exp Med 210:821–838. Darbas A, Jaegle M, Walbeehm E, van den Burg H, Driegen S, Broos L, Uyl M, Visser P, Grosveld F, Meijer D (2004) Cell autonomy of the mouse claw paw mutation. Dev Biol 272:470–482. de Bellescize J, Boutry N, Chabrol E, Andre-Obadia N, Arzimanoglou A, Leguern E, Baulac S, Calender A, Ryvlin P, Lesca G (2009) A novel three base-pair LGI1 deletion leading to loss of function in a family with autosomal dominant lateral temporal epilepsy and migraine-like episodes. Epilepsy Res 85:118–122. Dehal P, Boore JL (2005) Two rounds of whole genome duplication in the ancestral vertebrate. PLoS Biol 3:e314. Delmaghani S, Aghaie A, Michalski N, Bonnet C, Weil D, Petit C (2012) Defect in the gene encoding the EAR/EPTP domain-containing protein TSPEAR causes DFNB98 profound deafness. Hum Mol Genet 21:3835–3844. Dhaunchak AS, Huang JK, De Faria Junior O, Roth AD, Pedraza L, Antel JP, Bar-Or A, Colman DR (2010) A proteome map of axoglial specializations isolated and purified from human central nervous system. Glia 58:1949–1960. Di Bonaventura C, Operto FF, Busolin G, Egeo G, D’Aniello A, Vitello L, Smaniotto G, Furlan S, Diani E, Michelucci R, Giallonardo AT, Coppola G, Nobile C (2011) Low penetrance and effect on protein secretion of LGI1 mutations causing autosomal dominant lateral temporal epilepsy. Epilepsia 52:1258–1264. Doretto MC, Cortes-de-Oliveira JA, Rossetti F, Garcia-Cairasco N (2009) Role of the superior colliculus in the expression of acute and kindled audiogenic seizures in Wistar audiogenic rats. Epilepsia 50:2563–2574. Fukata Y, Adesnik H, Iwanaga T, Bredt DS, Nicoll RA, Fukata M (2006) Epilepsy-related ligand/receptor complex LGI1 and ADAM22 regulate synaptic transmission. Science 313:1792–1795. Fukata Y, Lovero KL, Iwanaga T, Watanabe A, Yokoi N, Tabuchi K, Shigemoto R, Nicoll RA, Fukata M (2010) Disruption of LGI1-linked synaptic complex causes abnormal synaptic transmission and epilepsy. Proc Natl Acad Sci USA 107:3799–3804. 2013 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. LGI proteins Fulop V, Jones DT (1999) Beta propellers: structural rigidity and functional diversity. Curr Opin Struct Biol 9:715–721. Gabellini N, Masola V, Quartesan S, Oselladore B, Nobile C, Michelucci R, Curtarello M, Parolin C, Palu G (2006) Increased expression of LGI1 gene triggers growth inhibition and apoptosis of neuroblastoma cells. J Cell Physiol 207:711–721. Garcia-Cairasco N (2002) A critical review on the participation of inferior colliculus in acoustic-motor and acoustic-limbic networks involved in the expression of acute and kindled audiogenic seizures. Hear Res 168:208–222. Garcia-Cairasco N, Terra VC, Doretto MC (1993) Midbrain substrates of audiogenic seizures in rats. Behav Brain Res 58:57–67. Gillis WQ, St John J, Bowerman B, Schneider SQ (2009) Whole genome duplications and expansion of the vertebrate GATA transcription factor gene family. BMC Evol Biol 9:207. Gu W, Wevers A, Schroder H, Grzeschik KH, Derst C, Brodtkorb E, de Vos R, Steinlein OK (2002) The LGI1 gene involved in lateral temporal lobe epilepsy belongs to a new subfamily of leucine-rich repeat proteins. FEBS Lett 519:71–76. Gu W, Brodtkorb E, Piepoli T, Finocchiaro G, Steinlein OK (2005a) LGI1: a gene involved in epileptogenesis and glioma progression? Neurogenetics 6:59–66. Gu W, Gibert Y, Wirth T, Elischer A, Bloch W, Meyer A, Steinlein OK, Begemann G (2005b) Using gene-history and expression analyses to assess the involvement of LGI genes in human disorders. Mol Biol Evol 22:2209–2216. Han K, Kim E (2008) Synaptic adhesion molecules and PSD-95. Prog Neurobiol 84:263–283. Head K, Gong S, Joseph S, Wang C, Burkhardt T, Rossi MR, LaDuca J, Matsui S, Vaughan M, Hicks DG, Heintz N, Cowell JK (2007) Defining the expression pattern of the LGI1 gene in BAC transgenic mice. Mamm Genome 18:328–337. Heiman GA, Kamberakis K, Gill R, Kalachikov S, Pedley TA, Hauser WA, Ottman R (2010) Evaluation of depression risk in LGI1 mutation carriers. Epilepsia 51:1685–1690. Hellsten U, Harland RM, Gilchrist MJ, Hendrix D, Jurka J, Kapitonov V, Ovcharenko I, Putnam NH, Shu S, Taher L et al. (2010) The genome of the Western clawed frog Xenopus tropicalis. Science 328:633–636. Henry EW, Eicher EM, Sidman RL (1991) The mouse mutation claw paw: forelimb deformity and delayed myelination throughout the peripheral nervous system. J Hered 82:287–294. Ho YY, Ionita-Laza I, Ottman R (2012) Domain-dependent clustering and genotype-phenotype analysis of LGI1 mutations in ADPEAF. Neurology 78:563–568. Howitt JA, Clout NJ, Hohenester E (2004) Binding site for Robo receptors revealed by dissection of the leucine-rich repeat region of Slit. EMBO J 23:4406–4412. Irani SR, Vincent A (2011) Autoimmune encephalitis – new awareness, challenging questions. Discovery Med 11:449–458. Irani SR, Alexander S, Waters P, Kleopa KA, Pettingill P, Zuliani L, Peles E, Buckley C, Lang B, Vincent A (2010) Antibodies to Kv1 potassium channel-complex proteins leucine-rich, glioma inactivated 1 protein and contactin-associated protein-2 in limbic encephalitis, Morvan’s syndrome and acquired neuromyotonia. Brain 133:2734–2748. Irani SR, Michell AW, Lang B, Pettingill P, Waters P, Johnson MR, Schott JM, Armstrong RJ, A SZ, Bleasel A, Somerville ER, Smith SM, Vincent A (2011) Faciobrachial dystonic seizures precede Lgi1 antibody limbic encephalitis. Ann Neurol 69:892–900. Jaegle M, Mandemakers W, Broos L, Zwart R, Karis A, Visser P, Grosveld F, Meijer D (1996) The POU factor Oct-6 and Schwann cell differentiation. Science 273:507–510. Jawad Z, Paoli M (2002) Novel sequences propel familiar folds. Structure 10:447–454. Jessen KR (2004) Glial cells. Int J Biochem Cell Biol 36:1861–1867. Jokinen TS, Metsahonkala L, Bergamasco L, Viitmaa R, Syrja P, Lohi H, Snellman M, Jeserevics J, Cizinauskas S (2007) Benign familial juvenile epilepsy in Lagotto Romagnolo dogs. J Vet Int Med 21:464–471.  C Kalachikov S, Evgrafov O, Ross B, Winawer M, Barker-Cummings C, Martinelli Boneschi F, Choi C, Morozov P, Das K, Teplitskaya E, Yu A, Cayanis E, Penchaszadeh G, Kottmann AH, Pedley TA, Hauser WA, Ottman R, Gilliam TC (2002) Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features. Nat Genet 30:335–341. Kawamata J, Ikeda A, Fujita Y, Usui K, Shimohama S, Takahashi R (2010) Mutations in LGI1 gene in Japanese families with autosomal dominant lateral temporal lobe epilepsy: the first report from Asian families. Epilepsia 51:690–693. Kim HA, Park WJ, Jeong HS, Lee HE, Lee SH, Kwon NS, Baek KJ, Kim DS, Yun HY (2012) Leucine-rich glioma inactivated 3 regulates adipogenesis through ADAM23. Biochim Biophys Acta 1821:914–922. Kim HA, Kwon NS, Baek KJ, Kim DS, Yun HY (2013) Leucine-rich glioma inactivated 3 associates negatively with adiponectin. Cytokine 62:206–209. Kimura N, Ishii Y, Suzaki S, Negishi T, Kyuwa S, Yoshikawa Y (2007) Abeta upregulates and colocalizes with LGI3 in cultured rat astrocytes. Cell Mol Neurobiol 27:335–350. Kobayashi E, Santos NF, Torres FR, Secolin R, Sardinha LA, Lopez-Cendes I, Cendes F (2003) Magnetic resonance imaging abnormalities in familial temporal lobe epilepsy with auditory auras. Arch Neurol 60:1546– 1551. Kobe B, Kajava AV (2001) The leucine-rich repeat as a protein recognition motif. Curr Opin Struct Biol 11:725–732. Krex D, Hauses M, Appelt H, Mohr B, Ehninger G, Schackert HK, Schackert G (2002) Physical and functional characterization of the human LGI1 gene and its possible role in glioma development. Acta Neuropathol 103:255–266. Kunapuli P, Chitta KS, Cowell JK (2003) Suppression of the cell proliferation and invasion phenotypes in glioma cells by the LGI1 gene. Oncogene 22:3985–3991. Kunapuli P, Kasyapa CS, Hawthorn L, Cowell JK (2004) LGI1, a putative tumor metastasis suppressor gene, controls in vitro invasiveness and expression of matrix metalloproteinases in glioma cells through the ERK1/2 pathway. J Biol Chem 279:23151–23157. Kunapuli P, Lo K, Hawthorn L, Cowell JK (2010) Reexpression of LGI1 in glioma cells results in dysregulation of genes implicated in the canonical axon guidance pathway. Genomics 95:93–100. Kusuzawa S, Honda T, Fukata Y, Fukata M, Kanatani S, Tanaka DH, Nakajima K (2012) Leucine-rich glioma inactivated 1 (Lgi1), an epilepsy-related secreted protein, has a nuclear localization signal and localizes to both the cytoplasm and the nucleus of the caudal ganglionic eminence neurons. Eur J Neurosci 36:2284–2292. Lai M, Huijbers MG, Lancaster E, Graus F, Bataller L, Balice-Gordon R, Cowell JK, Dalmau J (2010) Investigation of LGI1 as the antigen in limbic encephalitis previously attributed to potassium channels: a case series. Lancet Neurol 9:776–785. Lalic T, Pettingill P, Vincent A, Capogna M (2011) Human limbic encephalitis serum enhances hippocampal mossy fiber-CA3 pyramidal cell synaptic transmission. Epilepsia 52:121–131. Lee SE, Lee AY, Park WJ, Jun DH, Kwon NS, Baek KJ, Kim YG, Yun HY (2006) Mouse LGI3 gene: expression in brain and promoter analysis. Gene 372:8–17. Lee SH, Jeong YM, Kim SY, Jeong HS, Park KC, Baek KJ, Kwon NS, Yun HY, Kim DS (2012) Ultraviolet B-induced LGI3 secretion protects human keratinocytes. Exp Dermatol 21:716–718. Leonardi E, Andreazza S, Vanin S, Busolin G, Nobile C, Tosatto SC (2011) A computational model of the LGI1 protein suggests a common binding site for ADAM proteins. PLoS ONE 6:e18142. Li S, Yang Z, Hu J, Gordon WC, Bazan NG, Haas AL, Bok D, Jin M (2013) Secretory defect and cytotoxicity: the potential disease mechanisms for the retinitis pigmentosa (RP)-associated interphotoreceptor retinoid-binding protein (IRBP). J Biol Chem 288:11395– 11406. Limviphuvadh V, Chua LL, Rahim RA, Eisenhaber F, Maurer-Stroh S, Adhikari S (2010) Similarity of molecular phenotype between known epilepsy gene LGI1 and disease candidate gene LGI2. BMC Biochem 11:39. 2013 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. 179 L. Kegel and others Magdaleno S, Jensen P, Brumwell CL, Seal A, Lehman K, Asbury A, Cheung T, Cornelius T, Batten DM, Eden C, Norland SM, Rice DS, Dosooye N, Shakya S, Mehta P, Curran T (2006) BGEM: an in situ hybridization database of gene expression in the embryonic and adult mouse nervous system. PLoS Biol 4:e86. Manning G, Scheeff E (2010) How the vertebrates were made: selective pruning of a double-duplicated genome. BMC Biol 8:144. McMahon SA, Diaz E (2011) Mechanisms of excitatory synapse maturation by trans-synaptic organizing complexes. Curr Opin Neurobiol 21:221– 227. McMillan DR, White PC (2004) Loss of the transmembrane and cytoplasmic domains of the very large G-protein-coupled receptor-1 (VLGR1 or Mass1) causes audiogenic seizures in mice. Mol Cell Neurosci 26:322–329. Michelucci R, Pasini E, Malacrida S, Striano P, Bonaventura CD, Pulitano P, Bisulli F, Egeo G, Santulli L, Sofia V, Gambardella A, Elia M, de Falco A, Neve AL, Banfi P, Coppola G, Avoni P, Binelli S, Boniver C, Pisano T, Marchini M, Dazzo E, Fanciulli M, Bartolini Y, Riguzzi P, Volpi L, de Falco FA, Giallonardo AT, Mecarelli O, Striano S, Tinuper P, Nobile C (2013) Low penetrance of autosomal dominant lateral temporal epilepsy in Italian families without LGI1 mutations. Epilepsia, in the press. Morante-Redolat JM, Gorostidi-Pagola A, Piquer-Sirerol S, Sáenz A, Poza JJ, Galán J, Gesk S, Sarafidou T, Mautner VF, Binelli S, Staub E, Hinzmann B, French L, Prud’homme JF, Passarelli D, Scannapieco P, Tassinari CA, Avanzini G, Martı́-Massó JF, Kluwe L, Deloukas P, Moschonas NK, Michelucci R, Siebert R, Nobile C, Pérez-Tur J, López de Munain A (2002) Mutations in the LGI1/Epitempin gene on 10q24 cause autosomal dominant lateral temporal epilepsy. Hum Mol Genet 11:1119–1128. Nakayama J, Fu YH, Clark AM, Nakahara S, Hamano K, Iwasaki N, Matsui A, Arinami T, Ptacek LJ (2002) A nonsense mutation of the MASS1 gene in a family with febrile and afebrile seizures. Ann Neurol 52:654–657. Nave KA (2010) Myelination and support of axonal integrity by glia. Nature 468:244–252. Nicoll RA, Tomita S, Bredt DS (2006) Auxiliary subunits assist AMPA-type glutamate receptors. Science 311:1253–1256. Nishino J, Saunders TL, Sagane K, Morrison SJ (2010) Lgi4 promotes the proliferation and differentiation of glial lineage cells throughout the developing peripheral nervous system. J Neurosci 30:15228–15240. Nobile C, Michelucci R, Andreazza S, Pasini E, Tosatto SC, Striano P (2009) LGI1 mutations in autosomal dominant and sporadic lateral temporal epilepsy. Hum Mutat 30:530–536. Ohno S (1970) Evolution by gene duplication, Springer–Verlag, New York. Okabayashi S, Kimura N (2007) Immunohistochemical and biochemical analyses of LGI3 in monkey brain: LGI3 accumulates in aged monkey brains. Cell Mol Neurobiol 27:819–830. Okabayashi S, Kimura N (2008) Leucine-rich glioma inactivated 3 is involved in amyloid beta peptide uptake by astrocytes and endocytosis itself. NeuroReport 19:1175–1179. Okabayashi S, Kimura N (2010) LGI3 interacts with flotillin-1 to mediate APP trafficking and exosome formation. Neuroreport 21:606–610. Ottman R, Risch N, Hauser WA, Pedley TA, Lee JH, Barker-Cummings C, Lustenberger A, Nagle KJ, Lee KS et al. (1995) Localization of a gene for partial epilepsy to chromosome 10q. Nat Genet 10:56–60. Owuor K, Harel NY, Englot DJ, Hisama F, Blumenfeld H, Strittmatter SM (2009) LGI1-associated epilepsy through altered ADAM23-dependent neuronal morphology. Mol Cell Neurosci 42:448–457. Özkaynak E, Abello G, Jaegle M, van Berge L, Hamer D, Kegel L, Driegen S, Sagane K, Bermingham Jr, JR, Meijer D (2010) Adam22 is a major neuronal receptor for Lgi4-mediated Schwann cell signaling. J Neurosci 30:3857–3864. Paoli M (2001a) Protein folds propelled by diversity. Prog Biophys Mol Biol 76:103–130. Paoli M (2001b) An elusive propeller-like fold. Nat Struct Biol 8:744–745. Park WJ, Lee SE, Kwon NS, Baek KJ, Kim DS, Yun HY (2008) Leucine-rich glioma inactivated 3 associates with syntaxin 1. Neurosci Lett 444:240–244. Park WJ, Lim YY, Kwon NS, Baek KJ, Kim DS, Yun HY (2010) Leucine-rich glioma inactivated 3 induces neurite outgrowth through Akt and focal adhesion kinase. Neurochem Res 35:789–796. 180  C Peng D, Sheta EA, Powell SM, Moskaluk CA, Washington K, Goldknopf IL, El-Rifai W (2008) Alterations in Barrett’s-related adenocarcinomas: a proteomic approach. Int J Cancer 122:1303–1310. Piaton G, Gould RM, Lubetzki C (2010) Axon-oligodendrocyte interactions during developmental myelination, demyelination and repair. J Neurochem 114:1243–1260. Piepoli T, Jakupoglu C, Gu W, Lualdi E, Suarez-Merino B, Poliani PL, Cattaneo MG, Ortino B, Goplen D, Wang J, Mola R, Inverardi F, Frassoni C, Bjerkvig R, Steinlein O, Vicentini LM, Brustle O, Finocchiaro G (2006) Expression studies in gliomas and glial cells do not support a tumor suppressor role for LGI1. Neuro Oncol 8:96–108. Plantone D, Renna R, Grossi D, Plantone F, Iorio R (2013) Teaching NeuroImages: basal ganglia involvement in facio-brachial dystonic seizures associated with LGI1 antibodies. Neurology 80:e183– e184. Pons T, Gomez R, Chinea G, Valencia A (2003) Beta-propellers: associated functions and their role in human diseases. Curr Med Chem 10:505–524. Poza JJ, Saenz A, Martinez-Gil A, Cheron N, Cobo AM, Urtasun M, Marti-Masso JF, Grid D, Beckmann JS, Prud’homme JF, Lopez de Munain A (1999) Autosomal dominant lateral temporal epilepsy: clinical and genetic study of a large Basque pedigree linked to chromosome 10q. Ann Neurol 45:182–188. Quintes S, Goebbels S, Saher G, Schwab MH, Nave KA (2010) Neuron-glia signaling and the protection of axon function by Schwann cells. J Peripher Nerv Syst 15:10–16. Ribeiro PA, Sbragia L, Gilioli R, Langone F, Conte FF, Lopes-Cendes I (2008) Expression profile of Lgi1 gene in mouse brain during development. J Mol Neurosci 35:323–329. Rosanoff MJ, Ottman R (2008) Penetrance of LGI1 mutations in autosomal dominant partial epilepsy with auditory features. Neurology 71:567– 571. Rossi MR, Huntoon K, Cowell JK (2005) Differential expression of the LGI and SLIT families of genes in human cancer cells. Gene 356:85–90. Roussel BD, Kruppa AJ, Miranda E, Crowther DC, Lomas DA, Marciniak SJ (2013) Endoplasmic reticulum dysfunction in neurological disease. Lancet Neurol 12:105–118. Sagane K, Hayakawa K, Kai J, Hirohashi T, Takahashi E, Miyamoto N, Ino M, Oki T, Yamazaki K, Nagasu T (2005) Ataxia and peripheral nerve hypomyelination in ADAM22-deficient mice. BMC Neurosci 6:33. Sagane K, Ishihama Y, Sugimoto H (2008) LGI1 and LGI4 bind to ADAM22, ADAM23 and ADAM11. Int J Biol Sci 4:387–396. Sagane K, Sugimoto H, Akaike A (2010) Biological characterization of ADAM22 variants reveals the importance of a disintegrin domain sequence in cell surface expression. J Recept Signal Transduct Res 30:72–77. Scheel H, Tomiuk S, Hofmann K (2002) A common protein interaction domain links two recently identified epilepsy genes. Hum Mol Genet 11:1757–1762. Schulte U, Thumfart JO, Klocker N, Sailer CA, Bildl W, Biniossek M, Dehn D, Deller T, Eble S, Abbass K, Wangler T, Knaus HG, Fakler B (2006) The epilepsy-linked Lgi1 protein assembles into presynaptic Kv1 channels and inhibits inactivation by Kvbeta1. Neuron 49:697–706. Seals DF, Courtneidge SA (2003) The ADAMs family of metalloproteases: multidomain proteins with multiple functions. Genes Dev 17:7–30. Senechal KR, Thaller C, Noebels JL (2005) ADPEAF mutations reduce levels of secreted LGI1, a putative tumor suppressor protein linked to epilepsy. Hum Mol Genet 14:1613–1620. Seppälä EH, Jokinen TS, Fukata M, Fukata Y, Webster MT, Karlsson EK, Kilpinen SK, Steffen F, Dietschi E, Leeb T, Eklund R, Zhao X, Rilstone JJ, Lindblad-Toh K, Minassian BA, Lohi H (2011) LGI2 truncation causes a remitting focal epilepsy in dogs. PLoS Genet 7:e1002194. Seppälä EH, Koskinen LL, Gullov CH, Jokinen P, Karlskov-Mortensen P, Bergamasco L, Baranowska Korberg I, Cizinauskas S, Oberbauer AM, Berendt M, Fredholm M, Lohi H (2012) Identification of a novel idiopathic epilepsy locus in Belgian Shepherd dogs. PLoS ONE 7:e33549. Siddiqui TJ, Craig AM (2011) Synaptic organizing complexes. Curr Opin Neurobiol 21:132–143. 2013 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. LGI proteins Sirerol-Piquer MS, Ayerdi-Izquierdo A, Morante-Redolat JM, Herranz-Perez V, Favell K, Barker PA, Perez-Tur J (2006) The epilepsy gene LGI1 encodes a secreted glycoprotein that binds to the cell surface. Hum Mol Genet 15:3436–3445. Skradski SL, Clark AM, Jiang H, White HS, Fu YH, Ptacek LJ (2001) A novel gene causing a mendelian audiogenic mouse epilepsy. Neuron 31:537– 544. Staub E, Perez-Tur J, Siebert R, Nobile C, Moschonas NK, Deloukas P, Hinzmann B (2002) The novel EPTP repeat defines a superfamily of proteins implicated in epileptic disorders. Trends Biochem Sci 27:441–444. Striano P, Busolin G, Santulli L, Leonardi E, Coppola A, Vitiello L, Rigon L, Michelucci R, Tosatto SC, Striano S, Nobile C (2011) Familial temporal lobe epilepsy with psychic auras associated with a novel LGI1 mutation. Neurology 76:1173–1176. Suga K, Yamamori T, Akagawa K (2003) Identification of the carboxyl-terminal membrane-anchoring region of HPC-1/syntaxin 1A with the substituted-cysteine-accessibility method and monoclonal antibodies. J Biochem 133:325–334. Takahashi E, Sagane K, Nagasu T, Kuromitsu J (2006a) Altered nociceptive response in ADAM11-deficient mice. Brain Res 1097:39–42. Takahashi E, Sagane K, Oki T, Yamazaki K, Nagasu T, Kuromitsu J (2006b) Deficits in spatial learning and motor coordination in ADAM11-deficient mice. BMC Neurosci 7:19. Teng Y, Xie X, Walker S, Rempala G, Kozlowski DJ, Mumm JS, Cowell JK (2010) Knockdown of zebrafish Lgi1a results in abnormal development, brain defects and a seizure-like behavioral phenotype. Hum Mol Genet 19:4409–4420. Teng Y, Xie X, Walker S, Saxena M, Kozlowski DJ, Mumm JS, Cowell JK (2011) Loss of zebrafish lgi1b leads to hydrocephalus and sensitization to pentylenetetrazol induced seizure-like behavior. PLoS ONE 6:e24596. Tessa C, Michelucci R, Nobile C, Giannelli M, Della Nave R, Testoni S, Bianucci D, Tinuper P, Bisulli F, Sofia V, De Feo MR, Giallonardo AT, Tassinari CA, Mascalchi M (2007) Structural anomaly of left lateral temporal lobe in epilepsy due to mutated LGI1. Neurology 69:1298–1300. Thomas R, Favell K, Morante-Redolat J, Pool M, Kent C, Wright M, Daignault K, Ferraro GB, Montcalm S, Durocher Y, Fournier A, Perez-Tur J, Barker PA (2010) LGI1 is a Nogo receptor 1 ligand that antagonizes myelin-based growth inhibition. J Neurosci 30:6607–6612. Tomita S, Adesnik H, Sekiguchi M, Zhang W, Wada K, Howe JR, Nicoll RA, Bredt DS (2005) Stargazin modulates AMPA receptor gating and trafficking by distinct domains. Nature 435:1052–1058. Tuzun E, Dalmau J (2007) Limbic encephalitis and variants: classification, diagnosis and treatment. Neurologist 13:261–271. Van de Peer Y, Maere S, Meyer A (2009) The evolutionary significance of ancient genome duplications. Nat Rev Genet 10:725–732. Vincent A, Bien CG, Irani SR, Waters P (2011) Autoantibodies associated with diseases of the CNS: new developments and future challenges. Lancet Neurol 10:759–772. Waites CL, Craig AM, Garner CC (2005) Mechanisms of vertebrate synaptogenesis. Annu Rev Neurosci 28:251–274. Wang J, Valo Z, Bowers CW, Smith DD, Liu Z, Singer-Sam J (2010) Dual DNA methylation patterns in the CNS reveal developmentally poised chromatin and monoallelic expression of critical genes. PLoS ONE 5:e13843. Winawer MR, Ottman R, Hauser WA, Pedley TA (2000) Autosomal dominant partial epilepsy with auditory features: defining the phenotype. Neurology 54:2173–2176. Winawer MR, Martinelli Boneschi F, Barker-Cummings C, Lee JH, Liu J, Mekios C, Gilliam TC, Pedley TA, Hauser WA, Ottman R (2002) Four new families with autosomal dominant partial epilepsy with auditory features: clinical description and linkage to chromosome 10q24. Epilepsia 43:60–67. Xu C, Min J (2011) Structure and function of WD40 domain proteins. Protein Cell 2:202–214. Yang P, Baker KA, Hagg T (2006) The ADAMs family: coordinators of nervous system development, plasticity and repair. Prog Neurobiol 79:73–94. Yokoi N, Fukata M, Fukata Y (2012) Synaptic plasticity regulated by protein–protein interactions and posttranslational modifications. Int Rev Cell Mol Biol 297:1–43. Yu YE, Wen L, Silva J, Li Z, Head K, Sossey-Alaoui K, Pao A, Mei L, Cowell JK (2010) Lgi1 null mutant mice exhibit myoclonic seizures and CA1 neuronal hyperexcitability. Hum Mol Genet 19:1702–1711. Zhou YD, Lee S, Jin Z, Wright M, Smith SE, Anderson MP (2009) Arrested maturation of excitatory synapses in autosomal dominant lateral temporal lobe epilepsy. Nat Med 15:1208–1214. Zhou YD, Zhang D, Özkaynak E, Wang X, Kasper EM, Leguern E, Baulac S, Anderson MP (2012) Epilepsy gene LGI1 regulates postnatal developmental remodeling of retinogeniculate synapses. J Neurosci 32:903–910. Received 2 January 2013/22 May 2013; accepted 28 May 2013 Published as Immediate Publication 28 May 2013, doi 10.1042/AN20120095  C 2013 The Author(s) This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (CC-BY) (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution and reproduction in any medium, provided the original work is properly cited. View publication stats 181