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Eukaryogenesis

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This is an old revision of this page, as edited by Chiswick Chap (talk | contribs) at 12:24, 12 April 2023 (Last eukaryotic common ancestor (LECA): ESCRT proteins, ref Makarova 2010). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

LUCA and LECA: the origins of the eukaryotes.[1] The point of fusion (marked "?") below LECA is the FECA, the first eukaryotic common ancestor, some 2.2 billion years ago. Much earlier, some 4 billion years ago, the LUCA gave rise to the two domains of prokaryotes, the bacteria and the archaea.

Eukaryogenesis, the process which created the eukaryotic cell and lineage, is a milestone in the evolution of life, since eukaryotes include all complex cells and almost all multicellular organisms. The process is widely agreed to have involved symbiogenesis, in which archaea and bacteria came together to create the first eukaryotic common ancestor (FECA). This cell had a new level of complexity and capability, with a nucleus, at least one centriole and cilium, facultatively aerobic mitochondria, sex (meiosis and syngamy), a dormant cyst with a cell wall of chitin and/or cellulose and peroxisomes. It evolved into a population of single-celled organisms that included the last eukaryotic common ancestor (LECA), gaining capabilities along the way, though the sequence of the steps involved has been disputed.

Context

Life arose on Earth once it had cooled enough for oceans to form. The last universal common ancestor (LUCA) was an organism which had ribosomes and the genetic code; it lived some 4 billion years ago. It gave rise to two main branches of prokaryotic life, the bacteria and the archaea. From among these small-celled, rapidly-dividing ancestors arose the Eukaryotes, with much larger cells, nuclei, and distinctive biochemistry.[1][2] The eukaryotes form a domain that contains all complex cells and most types of multicellular organism, including the animals, plants, and fungi.[3][4]

Symbiogenesis

According to the theory of symbiogenesis, championed by Lynn Margulis, a member of the archaea gained a bacterial cell as a component. The archaeal cell was a member of the Asgard group. The bacterium was one of the Alphaproteobacteria, which had the ability to use oxygen in its respiration. This enabled it – and the archaeal cells that included it – to survive in the presence of oxygen, which was poisonous to other organisms adapted to reducing conditions. The endosymbiotic bacteria became the eukaryotic cell's mitochondria, providing most of the energy of the cell.[1] Lynn Margulis and colleagues have suggested that the cell also acquired a Spirochaete bacterium as a symbiont, providing the cell skeleton of microtubules and the ability to move, including the ability to pull chromosomes into two sets during mitosis, cell division.[5] Endosymbiosis with alphaproteobacteria created mitochondria, essentially universal among eukaryotes.[6]

Last eukaryotic common ancestor (LECA)

The last eukaryotic common ancestor (LECA) is the hypothetical last common ancestor of all living eukaryotes,[3][4] and was most likely a biological population.[7] It is believed to have been a protist with a nucleus, at least one centriole and cilium, facultatively aerobic mitochondria, sex (meiosis and syngamy), a dormant cyst with a cell wall of chitin and/or cellulose, and peroxisomes.[8][9]

It had been proposed that the LECA fed by phagocytosis, engulfing other organisms.[10][9] However, in 2022, Nico Bremer and colleagues confirmed that the LECA had mitochondria, and stated that it had multiple nuclei, but disputed that it was phagotrophic, meaning that the ability found in many eukaryotes to engulf materials developed later, rather than being acquired first and then being used to engulf the alphaproteobacteria that became mitochondria.[11]

The LECA has been described as having "spectacular cellular complexity".[12] Its cell was divided into compartments.[12] It appears to have inherited a set of ensosomal sorting complex (ESCRT) proteins that enable membranes to be remodelled, including pinching off vesicles.[13] Its apparatus for transcribing DNA into RNA, and then translating the RNA into proteins, were separated, allowing the expression of genes to become more complex. It had mechanisms for reshuffling its genetic material and possibly manipulating its own evolvability. All of these gave the LECA "a compelling cohort of selective advantages".[12]

Scenarios

Biologists have proposed multiple scenarios for the creation of the eukaryotes. While there is broad agreement that the LECA must have had a nucleus, mitochondria, and internal membranes, the order in which these were acquired has been disputed. In the syntrophic model, the first eukaryotic common ancestor (FECA) gained mitochondria, then membranes, then a nucleus. In the phagotrophic model, it gained a nucleus, then membranes, then mitochondria. In a more complex process, it gained all three in short order, then other capabilities. Other models have been proposed. Whatever happened, many lineages must have been created, but the LECA either out-competed or came together with the other lineages to form a single point of origin for the eukaryotes.[12] Nick Lane and William Martin have argued that mitochondria came first, on the grounds that energy had been the limiting factor on the size of the prokaryotic cell.[14] The phagotrophic model presupposes the ability to engulf food, enabling the cell to engulf the aerobic bacterium that became the mitochondrion.[12]

References

  1. ^ a b c McGrath, Casey (31 May 2022). "Highlight: Unraveling the Origins of LUCA and LECA on the Tree of Life". Genome Biology and Evolution. 14 (6). doi:10.1093/gbe/evac072.
  2. ^ Weiss, Madeline C.; Sousa, F. L.; Mrnjavac, N.; et al. (2016). "The physiology and habitat of the last universal common ancestor" (PDF). Nature Microbiology. 1 (9): 16116. doi:10.1038/nmicrobiol.2016.116. PMID 27562259. S2CID 2997255.
  3. ^ a b Gabaldón, T. (October 2021). "Origin and Early Evolution of the Eukaryotic Cell". Annual Review of Microbiology. 75 (1): 631–647. doi:10.1146/annurev-micro-090817-062213. PMID 34343017. S2CID 236916203.
  4. ^ a b Woese, C.R.; Kandler, O.; Wheelis, M.L. (June 1990). "Towards a natural system of organisms: proposal for the domains Archaea, Bacteria, and Eucarya". Proceedings of the National Academy of Sciences of the United States of America. 87 (12): 4576–4579. Bibcode:1990PNAS...87.4576W. doi:10.1073/pnas.87.12.4576. PMC 54159. PMID 2112744.
  5. ^ Margulis, Lynn; Chapman, Michael; Guerrero, Ricardo; Hall, John (29 August 2006). "The last eukaryotic common ancestor (LECA): Acquisition of cytoskeletal motility from aerotolerant spirochetes in the Proterozoic Eon". Proceedings of the National Academy of Sciences. 103 (35): 13080–13085. Bibcode:2006PNAS..10313080M. doi:10.1073/pnas.0604985103. PMC 1559756. PMID 16938841.
  6. ^ Latorre, A.; Durban, A; Moya, A.; Pereto, J. (2011). "The role of symbiosis in eukaryotic evolution". In Gargaud, Muriel; López-Garcìa, Purificacion; Martin H. (eds.). Origins and Evolution of Life: An astrobiological perspective. Cambridge: Cambridge University Press. pp. 326–339. ISBN 978-0-521-76131-4. Archived from the original on 24 March 2019. Retrieved 27 August 2017.
  7. ^ O'Malley, Maureen A.; Leger, Michelle M.; Wideman, Jeremy G.; Ruiz-Trillo, Iñaki (18 February 2019). "Concepts of the last eukaryotic common ancestor". Nature Ecology & Evolution. 3 (3): 338–344. doi:10.1038/s41559-019-0796-3. hdl:10261/201794. PMID 30778187. S2CID 256718457.
  8. ^ Leander, B. S. (May 2020). "Predatory protists". Current Biology. 30 (10): R510–R516. doi:10.1016/j.cub.2020.03.052. PMID 32428491. S2CID 218710816.
  9. ^ a b Strassert, Jürgen F. H.; Irisarri, Iker; Williams, Tom A.; Burki, Fabien (25 March 2021). "A molecular timescale for eukaryote evolution with implications for the origin of red algal-derived plastids". Nature Communications. 12 (1): 1879. Bibcode:2021NatCo..12.1879S. doi:10.1038/s41467-021-22044-z. PMC 7994803. PMID 33767194.
  10. ^ Leander, B. S. (May 2020). "Predatory protists". Current Biology. 30 (10): R510–R516. doi:10.1016/j.cub.2020.03.052. PMID 32428491. S2CID 218710816.
  11. ^ Bremer, Nico; Tria, Fernando D. K.; Skejo, Josip; Garg, Sriram G.; Martin, William F. (31 May 2022). "Ancestral State Reconstructions Trace Mitochondria But Not Phagocytosis to the Last Eukaryotic Common Ancestor". Genome Biology and Evolution. 14 (6). doi:10.1093/gbe/evac079. PMC 9185374. PMID 35642316.
  12. ^ a b c d e Koumandou, V. Lila; Wickstead, Bill; Ginger, Michael L.; van der Giezen, Mark; Dacks, Joel B.; Field, Mark C. (2013). "Molecular paleontology and complexity in the last eukaryotic common ancestor". Critical Reviews in Biochemistry and Molecular Biology. 48 (4): 373–396. doi:10.3109/10409238.2013.821444. PMC 3791482. PMID 23895660.
  13. ^ Makarova, Kira S.; Yutin, Natalya; Bell, Stephen D.; Koonin, Eugene V. (6 September 2010). "Evolution of diverse cell division and vesicle formation systems in Archaea". Nature Reviews Microbiology. 8 (10): 731–741. doi:10.1038/nrmicro2406.
  14. ^ Lane, Nick; Martin, William (2010). "The energetics of genome complexity". Nature. 467 (7318): 929–934. Bibcode:2010Natur.467..929L. doi:10.1038/nature09486. PMID 20962839. S2CID 17086117.