RNA Synthesis March 20

Topics To Be Covered
RNA Synthesis, Processing, Central dogma.

& Modification The structure of the gene;

 Gene Promoter
Transcription Apparatus;
 RNA Polymerase

RNA synthesis (Transcription).

Post-transcriptional processing of RNA
UNIVERSITY OF LIBERIA Regulation & Antibiotic Inhibitors of
A.M. Dogliotti College of Medicine
Department of Medical Biochemistry
By Mehidi K. Asst. Prof of Biochemistry 2019/20
Transcription
Mehidi K. 3

RNA is synthesized from a DNA template

Learning Objectives


 by an RNA Polymerase
 After reading this chapter you should be able
to:  the processes of DNA & RNA synthesis
 Describe the major steps in transcription of an  are similar in that they involve:
RNA molecule.
1. The general steps of initiation, elongation, &
 Explain the function of the different RNA termination with 5' to 3' polarity
polymerase enzymes.
2. Large, multicomponent initiation complexes
 Describe the different processing & splicing
events; 3. Adherence to Watson-Crick base-pairing rules
 that occur during synthesis of eukaryotic mRNAs.

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 These processes differ in several important Transcription (RNA Synthesis)

ways, including the following:  The structure of the gene: Fig-1
1.Ribonucleotides are used in RNA synthesis rather  The transcription unit (i.e., a gene) is a sequence
than deoxyribonucleotides (stretch) of DNA, which consists of:
a) the regulatory gene response sequences
2. U replaces T as the complementary bp for A in RNA (enhancer/silencer),
3.a primer is not involved in RNA synthesis b) the basal rate controlling sequence (the promoter),
c) the transcription initiation start point,
4.only a portion of the genome is transcribed or d) the gene proper, and
copied into RNA, e) the transcription termination sequence
 whereas the entire genome must be copied during DNA  b/n genes or islands of related genes there are
replication; insulator sequences;
5.there is no proofreading function during RNA  that separate the coordinately regulated gene(s)
 so as regulatory sequences would work only on these
transcription isolated gene(s)
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 The process of synthesizing RNA from a A. The gene enhancer/silencer,

DNA template:  are cis-acting response sequences
 has been characterized best in prokaryotes  that regulate the rate of gene expression through
 specific binding into transacting basal transcription
 Although in mammalian cells; machinery regulatory proteins.
 the regulation of RNA synthesis & the processing of the B. The gene promoter region or
RNA transcripts are different from those in prokaryotes,
 transcription initiator sequence up-stream the gene
 The process of RNA synthesis per se is; proper
 quite similar in these two classes of organisms  provides the region of binding of the RNA polymerase
The description of RNA synthesis in prokaryotes, C. Transcribed region or gene proper,
 where it is better understood,  the DNA sequence that is copied as hnRNA or
 is applicable to eukaryotes even though;  other types of RNAs that is mostly composed of
 introns & exons in eukaryotes,
 the enzymes involved & the regulatory signals,
though related, are different  but introns-containing genes are very rare in prokaryotes
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D. Termination region, Structure & Function of the Gene Promoter

 It is transcription initiator sequence
 a regulatory DNA sequence down-stream the gene
 works in the same orientation of the gene reading
proper of some genes, at w/c; frame (3'5')
 the RNA polymerase disassembles from the DNA template  is located in a close continuity with the gene proper
 RNA polymerase binds DNA template at the gene
TCCGGTAATTTGGGCGCTAATTTCCCG
5' 3' Coding Strand promoter:
AGGCCATTAAACCCGCGATTAAAGGGC  to initiate the basal (unregulated) rate of transcription
3' 5' Template Strand
Enlancer/ Terminator  Some promoters are weak & others are strong,
silencer/ Gene proper sequence  with a rate of transcription that is much faster
Promoter  nevertheless there are certain promoter less genes
 One gene may also have more than one promoter;
UCCGGUAAUUUGGGCGCUAAUUUCCCG
5' 3'RNATranscript  to be used differentially according to tissue specific needs

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 RNA polymerase also must recognize which genes to transcribe Characteristics of Prokaryotic Promoter in
 b/c transcribed genes are only a small fraction of the total DNA
 the genes that are transcribed:
the E coli
 differ from one type of cell to another &  it is the region recognized by RNA polymerases
 change with changes in physiologic conditions  it is simpler than eukaryotic promoter
 The signals in DNA that RNA polymerase recognizes are  is formed of three parts: Fig-2
called promoters;
 promoters are sequences in DNA (often composed of smaller i. Pribnow or TATA box:
sequences called boxes or elements)  It is a 6 bp stretch; 5'-TATAAT-3'
 that determine the start point & the frequency of transcription  located 10 nt upstreams the transcription start
 b/c they are located on the same molecule of DNA and near the site
gene they regulate,
ii.The spacer stretches of nucleotides of:
 they are said to be cis acting (i.e., “cis” refers to acting on the same side)
 about 10 bp in b/n the Transcription start & Pribnow box
 Proteins that bind to these DNA sequences & facilitate or prevent
the binding of RNA polymerase,  about 19 nt in b/n the Pribnow box & the -35 region,
 are said to be trans acting Fig-on next slide
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iii.The -35 region:  Still ~25% of the genes have:

 Initiator sequence &
 It is a stretch of 8 nt; 5'-TGTTGACA-3'
 Downstream promoter sequence; A/GGA/TCGTG,
 Located about 35 nt upstream the transcription start
 25 bp downstream transcription start site
site
 The remaining ~15 of the genes contain the 3
 Both Pribnow box & the -35 region are elements:
 recognized by RNA polymerases
 TATA, initiator & downstream promoter sequences
 These elements determine where transcription
-35 -10 starts;
DNA TGTTGACA 19 nucleotides TATAAT 10 nucleotides +1 RNA Transcription Start  through the binding of the:
 TATA binding protein (TBP) & its
-35 Region Pribnow Box associating factors (TAFs)
 that form the TFIID complex,
Sequences recognized by RNA Polymerase
 to recruit the RNA polymerase
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Example of Eukaryotic Promoter: ii. The spacer stretches of about;

 it is more complex than the prokaryotic one  25 bp DNA b/n the transcription start & TATA box
 consists of at least 3 parts:
 40 nucleotides b/n the CAAT box & TATA box
i. Hogness or TATA box: Fig-2a
 It is an 8 bp stretch of DNA, e.g., 5'-TATAAAAG-3' iii.cis-acting upstream promoter elements:
 located 25-30 nt upstream the transcription start site
 e.g., CAAT box,
 ~30% of the eukaryotic genes do not have TATA box;
 instead they have Initiator Sequence that spans the  a 9 bp stretch of nucleotides; 5'-GGNCAATCT-3'
transcription start site –3 to +5,
 located about 70 to 80 nt upstreams the site for
 e.g.,TCAG/TTT/C start of transcription and
 ~30% of the stronger genes have both:
 TATA & Initiator Sequences
 GC boxes, e.g., 5'-GGGCGG-3’

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 Specific trans-activating proteins;  The response elements may:

 bind these elements by their DNA-binding domain  activate transcription above the basal rate,
 interact with basal transcription machinery through their
are called Enhancer elements or
trans-activation domains
 They control the frequency of transcription:  suppress transcription below the basal rate,

 initiation for the basal rate of expression are called Silencer/Repressor elements

 Depending on their type, they are less rigid in:  They mediate responses to various signals;
 their orientation dependency than the TATA box group  Including:
 hormones,
-70 -25 -3 Initiator +5 +25 Downstream Promoter
 environmental changes &
DNA GGNCAATCT TATAAAAG TCAG/TTT/C A/GGA/TCGTG  toxins such as dioxin
CAAT Box TATA Box +1 RNA Transcription Start  though interaction with a large number of specific
37 nucleotides 25 nucleotides
transcription factors
Sequences recognized by RNA Polymerase
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Gene Response Elements (Enhancer or  The best examples for these elements are the
hormone-response elements:
Silencer)
 for steroid-thyroid superfamily of hormones,
 are transcription regulatory sequences that may be:  including vitamins D &A
 remote from the gene by hundreds or thousands of nt’s;
Transcription Factors:
 up- or down-stream the gene proper, or
 are activator or suppressor proteins
 even within the transcription unit
 that bind at these elements & interact with:
 work in an orientation-independent manner  RNA polymerases directly or indirectly through
 There are hundreds of types of response elements;  coactivator or corepressor proteins
 to increase or decrease rate of transcription
 with rigid or flexible sequence

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 Transcription factors have certain specific kind of Structure & Types of Prokaryotic & Eukaryotic DNA-
secondary structures, dependent RNA Polymerases
 i.e., motifs for the interaction with the responsive  Transcription is the process of synthesis of
DNA elements
complementary RNA copies:
 Zinc-finger motif is one common secondary
structure for these factors  from specific regions along the length of gene DNA,
 Tens of these elements may work on one gene  i.e., the gene proper
with the transcription factors binding to them in:  using DNA-dependent RNA polymerase (RNAP) &
 a cooperative, agonistic, ribonucleotides

 synergistic or antagonistic fashion  The general characteristics of the RNAP from

eukaryotes & prokaryotes:
 This brings about the tissue-specific pattern of
gene expression:  are compared in the following Fig-A,B & Table-1
 such as albumin gene in the liver  they do not have proofreading ability
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 Genes usually have several regulatory elements but

some genes have none;
 such as the constitutional or housekeeping genes
 that have a constant rate of basal transcription
 The interaction & the mechanism of binding of transcription factors with the
responsive elements is depicted in figure below:

Fig-A. RNA polymerase (RNAP).

 Catalyzes the polymerization of ribonucleotides into an RNA sequence
that is complementary to the template strand of the gene.
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Table-1b. Nomenclature & Properties of Mammalian

Nuclear DNA-Dependent RNA Polymerases
Major Products Sensitivity to
-Amanitin, NB

rRNA Insensitive
High
mRNA, miRNA Sensitivity

tRNA + Intermediate
Sensitivity
Fig-B. Comparison of Three-Dimensional Structures of Bacterial & 5S rRNA, snRNA
Eukaryotic RNA Polymerases
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Table-1a. Comparison of General Characteristics of RNA  The mushrooms picked by Amanda Tin contained
Polymerase (RNAP) In Eukaryotes & Prokaryotes -amanitin, an inhibitor of eukaryotic RNA polymerases
 It is particularly effective at blocking the action of RNAP-II
RNAP In Prokaryotes RNAP In Eukaryotes
A single type of RNA polymerase 3 types of RNA polymerases;  This toxin initially causes GI disturbances, then:
 that is responsible for synthesis of all  each is specific for the synthesis of a  electrolyte imbalance & fever,
types of RNA specific type of RNA  followed by liver & kidney dysfunction
Products of RNA polymerase require Mostly require extensive  b/n 40 & 90% of the individuals who ingest -amanitin
 slight or no modification after  post-transcriptional modifications  die within a few days NB
transcription particularly in mRNA
The holoenzyme is formed of five They are much complex in structure
subunits:
 two identical  subunits,  formed of 2 large (homologous to
 two similar but not identical ' the
') & up to 14 small subunits
The 3 types of RNA polymerases are:
catalytic subunits &
 a regulatory  subunit (2')  RNA polymerase I
 RNA polymerase II
The core part of the enzyme is formed
of the four 2' subunits.  RNA polymerase III
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Steps of Transcription Fig-TT  RNA polymerase recognizes the promoter

region:
I. Initiation Fig-IE
 occurs on a single strand of a transcription unit (a  by the help of the  (sigma) factor Fig-3a
gene) that is;
 called template (non-coding or non-sense) strand
 that then recruits the core enzyme (2') for
tight binding into DNA
 complementary to the RNA,
 it never occurs in the other strand,  There are several types to  factors:
 non-template, coding or sense strand
 that recognize different promoters
 coding strand is similar to mRNA sequence,
 except for U/T exchange  to differentially control gene transcription;
 according to the growth & environmental conditions
of the bacterium
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 The core enzyme unwinds 17-20 bp nt;

 ~60 bp in eukaryotes, from –30 to +30,
 to separate the two strands
 i.e., the transcription bubble Fig-IE
 The template strand is read in 3'5'  this requires:
 so that the synthesized RNA will be formed in  unwindase, disruption of the nucleosome structure
5'3’  the participation of topoisomerases
 w/c DNA strand is the template & w/c is the  The enzyme complex then;
coding,  searches for the transcription initiation site
 differs from one gene to the other  an open reading frame starting at TAC
 but is always the strand that contains the  this process requires:
prompter sequence read in 3'5' direction  participation of topoisomerases

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 The synthesized RNA:  with the release of a PPi each time

 always starts with a purine that enters at,  a new nt is added to the growing RNA chain
 the initiation site of the enzyme  Pyrophosphatases hydrolyze PPi into 2 Pi;
 this 5’-purine ribonucleotide at the 5’ end;  to ensure irreversibility of the polymerization
 retains its triphosphate & stays in mature mRNA
 When the 2nd nt enters at the elongation site  The RNA polymerase continues transcription
of the enzyme; Fig-3b  from 3' towards 5' end of the template strand
 it forms a phosphodiester bond b/n:  according to the base pairing role in an anti-
 3'-OH group of ribose of the 1st nt & parallel manner Fig-3a,b
 5'-OH of the phosphate group on C5 of ribose of the
2nd nt  Elongation continues,
 While on the promoter, the polymerase;  through the termination sequence
 synthesizes 10 – 20 nt stretch of RNA
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II. Elongation: Fig-IE  This suggests that RNA polymerase has associated
with it;
 The  Factor is released before elongation
starts:  an "unwindase" activity that opens the DNA helix

 leading to core enzyme conformational change  The fact that the DNA double helix must unwind &
 that enables its translocation to clear the  the strands part at least transiently for transcription
promoter implies;
 some disruption of the nucleosome structure of eukaryotic
 The 4 ribonucleotides triphosphate; cells
 ATP, GTP, CTP & UTP
 Topoisomerase both precedes & follows the
 continue to enter into the polymerization (or progressing RNAP; Fig-3c
elongation) site of  unit
 to prevent the formation of super helical complexes
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b.rho-independent termination:
III.Termination of Transcription:
◦ The rho-independent termination, is similar to:
 Inaddition to knowing where to start  that described for eukaryotic transcription, except that;
transcription,  the secondary structure & sequences involved are much better
 RNA polymerase must have a defined site at w/c: characterized in bacterial cells
 to stop RNA synthesis,
◦ In rho-independent termination, a hairpin loop is
 so that the appropriate size of transcript is produced
formed; Fig-12b
 Transcription termination in bacterial cells
 just before a sequence of 6 to 8 uridine (U) residues
occurs by:
 near the 3' end of the newly synthesized RNA
 one of two well-characterized mechanisms
 the formation of this secondary structure dislodges,
a) rho () factor dependent or
 the RNA polymerase from the DNA template,
b) rho () factor independent
 resulting in termination of RNA synthesis in the U stretch
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a. rho-dependent termination :  In eukaryotic cells:

 The rho () factor: Fig-12a  termination is less well defined
 is an ATP-dependent RNA-stimulated helicase
 it appears to be somehow linked both to;
 that recognizes & binds the termination sequence (~40 bp)
 initiation & addition of the 3' polyA tail of mRNA
 in the template DNA,
 then; it disassembles the enzyme/RNA/DNA complex  could involve destabilization of the RNA-DNA complex
 The termination sequence may occur:  at a region of A–U base pairs
 hundreds of base-pairs downstream the site at w/c poly(A)  More than one RNAP molecule may transcribe;
tail is added in mRNA
 An RNA endonuclease cleaves;  the same template strand of a gene simultaneously,
 the primary RNA transcript at 15 - 31 bases 3’ of,  but the process is phased & spaced in such a way that:
 the cleavage consensus sequence, i.e., AAUAAA  at any one moment each is transcribing a different
 the poly(A) tail is added to this new 3’ end portion of the DNA sequence
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◦ The 3 eukaryotic RNA polymerases employ;  Rifamycin:

 binds to the core enzyme & occupy the substrate
 different mechanisms to terminate transcription, for e.g., binding site to inhibit,
RNA polymerase I uses a specific protein,  binding of the incoming nucleotides to the initiation
site of the prokaryotic system
 to terminate the transcription of rRNAs
 Actinomycin D:
whereas RNA polymerase III uses:  binds DNA template & inhibiting its transcription
 a specific termination sequence  by preventing translocation of RNAP along DNA

In contrast, RNA polymerase II is more versatile,  Streptoglydigin:

 it binds with the β subunit of prokaryotic RNAP
 utilizing both sequence & protein factors to  thus inhibits the elongation
facilitate:  Heparin:
 pausing of the polymerase &  is a poly anion & binds to the β’ subunit of the RNAP
& inhibits transcription in vitro
 termination of transcription Mehidi K. 41
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Regulation & Antibiotic Inhibitors of Post-Transcriptional Modification of

Transcription: RNA
◦ Processing of freshly synthesized transcript in the
 Covalent modification nucleus;
 is different depending upon the type of RNA
 RNAP are zinc containing metalloenzymes  hence processing of mRNA, tRNA & rRNA is discussed
separately
 Several RNAP;
 may transcribe same gene simultaneously
I. Processing of mRNA: Fig-6a,b
 but in a phase & spaced manner ◦ Eukaryotic crude transcript of mRNA produced in
the nucleus is called
 Eukaryotic RNAP & the other transcription
 pre-mRNA or heterogeneous nuclear RNA (hnRNA)
regulators are under control;
◦ The newly synthesized hnRNA might be a complex
 by activating phosphorylation  inactivating transcript;
dephosphorylation mechanisms
 carrying information about more than one RNA (i.e.,
polycistronic)
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… cont’d

 Further, transcript of the mRNA of the genes

could contain:
 the intervening sequences known as ‘Introns’
 w/c have to be removed
 the ‘Exons’ joined together (splicing)
 This transcript undergoes various modifications w/c
are also designed for:
 the purpose of identification of different type of
RNA &
NB.The Cap Structure in Eukaryotic mRNA.
 increasing the half life & rate of its usage The phosphates in blue originated from the original
RNA transcript;
Mehidi K. 45 The phosphate in black comes from GTP. Mehidi K. 47

 Post-transcriptional processing of mRNA includes: b. Addition of polyadenylate 3'-tailing: Fig-8a, 8b

 decreasing its size, 5'-capping & 3'-tailing along with the
post-maturation mRNA editing Fig-6a,b
 Addition of 20-250 polyadenylate tail at the 3'-end

a. Capping: S-58 Fig-7a,b  By the action of polyadenylate polymerase

 It is the prompt addition of 7-methyl-GTP to the 5'-  The enzyme 1st recognizes the specific polyA
end of hnRNA; addition signal;
 by guanylate transferase after its transcription  AAUAAA at the mRNA 3'-UTR,
 The cap is attached by 5' to 5' triphosphate linkage  where its endonuclease activity cuts extra sequences
 The function of this structure is: to 11 - 30 bases 3' downstream this signal.

 it enhances subsequent hnRNA processing & the  The tail protects 3'-end of mRNA from 3'5'
translation of mRNA, exonuclease &
 protects mRNA from the action of 5’  3’ exonucleases
& phosphatases facilitates mRNA transport into cytoplasm
controlling its half-life
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Fig-8. Synthesis of the poly(A) Spliceosome

tail:  An aggregation formed in the nucleus of hnRNA,
 As RNA polymerase continues to  i.e., the blue script of mRNA or tRNA + 4 snRNAs; U1, U2, U5
transcribe the DNA, enzymes; & U4/U6 + more than 60 proteins

 cleave the transcript (hnRNA) at  There are highly splice conserved consensus
a point: sequences at the 5'- & 3'-ends of essentially; Fig-9
 all intron-exon boundaries, e.g., 5’-GU/AG-3’
 10–20 nt’s beyond an AAUAAA
sequence,  The enzymatic activity of the spliceosome complex
 just before a run of Us (or Gs)
resides in the snRNAs; called ribozymes
 250 adenine nucleotides are then  Many introns are self-splicing, i.e.,
added to the:  they accurately & efficiently splice themselves without
requiring additional protein factors
 3’-end of the hnRNA, one
at a time,  Removal of introns facilitates the transport of;
 mature mRNA from the nucleus to the cytoplasm
 by poly(A) polymerase
Mehidi K. 49  otherwise it will be degraded in the nucleus Mehidi K. 51

… cont’d
Processing of eukaryotic mRNAs:
◦ A gene may contain 1 - 80 introns.
 Spliceosomes & lariats
◦ Essentially all human genes contain introns
◦ In the more complicated post-transcriptional  except the histone & the rRNA genes
processing of eukaryotic mRNAs,
◦ Most introns have no known cellular function
 sequences called introns (intervening sequences)
 but a few may encode functional RNAs or proteins
 are removed from the primary transcript &
 the remaining segments, termed exons (expressed sequences), ◦ Introns also allow recombination b/n
 are ligated, to form a functional RNA  exons of different genes, i.e., exon shuffling

◦ This process involves: ◦ Introns also may have regulatory role on

 a large complex of proteins & auxiliary RNAs called snRNAs  gene expression by have regulatory sequences
 w/c interact to form a spliceosome
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… cont’d
c. Intron Removal (RNA Splicing):
◦ The function of the five snRNAs (U1, U2, U4, U5, U6) in
 The removal of an intron & rejoining of 2 exons;
the spliceosome is: Table-Sp
 to help position reacting groups within the substrate  can be considered to occur in two steps Fig-10 , 11
mRNA molecule,
 The 1st step involves: Fig-10
 so that the introns can be removed & the appropriate
exons can be spliced together precisely  the breaking of the phosphodiester bond at the
◦ The snRNAs accomplish this task; exon/intron boundary
 by binding, through base-pairing interactions,  at the 5' end of the intron
 with the sites on the mRNA that represent  is accomplished by a transesterification rxn, w/c occurs
 intron/exon boundaries b/n the:
◦ Accompanying protein factors are responsible for;  2'-OH of an adenosine nt usually found about 30 nt from
the 3' end of the intron, &
 holding the reacting components together to facilitate the
rxn  phosphate in the phosphodiester bond of a guanosine
residue located at the 5' end of the intron
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… cont’d

Table-Sp. The function of snRNAs in the splicing  This rxn cleaves the nucleotide chain & produces a
branched structure in w/c; Fig-10
of mRNAs
 the adenine has 2', 3', & 5' phosphate groups.
snRNA Size Function
 The intron forms a looped structure
U1 165 nt Binds the 5'exon/intron boundary  similar in appearance to that of a cowboy's lariat
U2 185 nt Binds the branch site on the intron  The 2nd step in the rxn involves:
U4 145 nt Helps assemble the spliceosome  the cleavage of the phosphodiester bond
 at the 3' end of the intron,
U5 116 nt Binds the 3'intron/exon boundary
 w/c releases the lariat structure from the complex
U6 106 nt Helps assemble the spliceosome

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… cont’d
◦ Splicing is completed by the joining of
 the 3' end of one exon to the 5' end of the next
exon,
 through the formation of a regular 5'-3'
phosphodiester bond
◦ Typically, the 3' end of one exon will be
spliced to the 5' end of the next closest exon,
 producing a transcript that exhibits all the exons
in the order in w/c they were transcribed
Fig-TT.
The Transcription
Mehidi K. 57 Cycle In Bacteria 59
59

… cont’d
◦ However, depending on cell & tissue type,
 a single gene can give rise to multiple forms of mature
RNA transcripts
 by a process termed alternative RNA splicing

◦ In these instances, some exons may not be

represented in the final transcript,
 yielding an RNA that encodes a different protein.
◦ This process represents a major mechanism by w/c
Fig-1.
eukaryotic cells A Schematic View of
 control synthesis of different proteins from the same gene a Eukaryotic Gene, &
transcript in a cell- or tissue-specific manner Steps Required to
Produce a Protein
Mehidi K. 58 Product. Mehidi K. 60
60

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RNA Synthesis March 20

61 Fig-2a. Prokaryotic & Eukaryotic Promoters. Pu purine; Py pyrimidine-16

Mehidi K. 61 Fig-MT. Mechanism of Transcription. 63

Fig-UW. DNA Unwinding.

Fig-2b. Bacterial promoters, such as that from E coli shown here, share two
regions of highly conserved nucleotide sequence. Fig-TB.Transcription Bubble.
Mehidi K. 62 Mehidi K. 64

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RNA Synthesis March 20

Mechanism
Fig-3b. Transcription by RNA
polymerase in E. coli.
Fig-IE.Transcription Initiation & Elongation by E. coli RNA Note that this is essentially the same mechanism
polymerase. S-34, 39 Mehidi K. 65 67 used by DNA polymerases.
Mehidi K. 67

Fig-3b.
Polymerization
of
Ribonucleotides
by
RNA Polymerase
During
Transcription.
Mechanism
Fig-3a.
Transcription by
RNA polymerase in
E. coli. S-40 Mehidi K. 66
66 Mehidi K. 68

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RNA Synthesis March 20

Mechanism
Fig-3c.
Transcription
by RNA
polymerase
in E. coli. Fig-4a’. Mechanism For the Termination of Transcription by  Protein.
 This protein is an ATP-dependent helicase that binds the nascent RNA chain and pulls
it away from RNA polymerase and the DNA template.
Mehidi K. 69
69 Mehidi K. 71

Fig-4a. rho-Dependent Termination Fig-4b. rho-Independent Termination

70 72
70 72

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RNA Synthesis March 20

Fig-5. Primary Transcript.

 Cleavage of this transcript produces:
 5S, 16S, & 23S rRNA molecules & a tRNA molecule.
 Spacer regions are shown in yellow.
Mehidi K. 73 Fig-6c. Overview of mRNA Processing In Eukaryotes. 75

Fig-7a.
The 5’ cap of
mRNA.
a. 7-Methylguanosine
is joined to the 5’
end of almost all
eukaryotic mRNAs
in an unusual 5’,5’-
triphosphate
linkage.

Fig-PE. Transcription & Translation.

Mehidi K. 74 Mehidi K. 76

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RNA Synthesis March 20

Fig-7b.  The consensus sequences at the intron/exon

The 5’ cap of mRNA.
b. Generation of the
boundaries of the pre-mRNA
5’ cap involves;  are AGGU (AGGT in the DNA).
 4 to 5 separate
steps
 The sequences vary to some extent on the exon side
 adoHcy is S- of the boundaries,
adenosylhomocysteine
c. Synthesis of the cap  but almost all introns begin with a 5’ GU and end with a 3’
is carried out by AG
 enzymes tethered
to the CTD of Pol II
 The cap remains
tethered to the CTD
 through an
association with  Fig-9. Splice junctions in hnRNA.
the cap-binding
◦ The intron sequences shown in blue dashed boxes are invariant
complex (CBC)
 They always appear at this position in introns.
◦ The sequences on the exon side of the splice sites are more variable
Mehidi K. 77 Mehidi K. 79

Fig-8b
Addition of the
poly(A) tail to
the primary RNA
transcript
of eukaryotes.

78

80 Fig-10. Splicing Process-6780

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RNA Synthesis March 20

Fig-10. Splicing process.

◦ snRNAs (U1 to U6) bind to the intron, causing it to
form a loop;
 The complex is called a splicesosome
◦ The U1 binds near the 1st exon/intron junction,
◦ U2 binds within the intron in a region containing
 an adenine nt residue
◦ Another group of snRNAs, U4, U5, & U6, binds
 to the complex, & the loop is formed. Fig-11. Splicing
◦ The phosphate attached to the G residue at the 5’- mechanism in mRNA
primary transcripts.
end of the intron forms a 2’–5’ linkage;
 with the 2’-OH group of the adenine nt residue
Mehidi K. 81 83

… cont’d

◦ Cleavage occurs at the end of the 1st exon, b/n: Fig-11. Splicing mechanism in mRNA
 the AG residues at the 3’ end of the exon & the GU primary transcripts.
residues at the 5’ end of the intron a. RNA Pairing Interactions in the
Formation of Spliceosome Complexes.
◦ The complex continues to be held in place by the b. Assembly Of Spliceosomes.
spliceosome. c. Coordination of splicing with
transcription provides an attractive
◦ A 2nd cleavage occurs at; mechanism for bringing the two splice
sites together.
 the 3’-end of the intron after the AG sequence.
◦ The exons are joined together.
◦ The intron, shaped like a lariat,
 is released & degraded to nucleotides

Mehidi K. 82 (c) 84

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Fig-14. rRNA &

85 Fig-12. Overview of mRNA Synthesis. 85 87 Ribosome Synthesis
87

86 Fig-13. Overview of tRNA Synthesis

86

Mehidi Kassim, Asst. Professor of Biochemistry 22