Splicing
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Figure 14.3 mouse globin mRNA PRECURSOR RNA hybridized to cloned gene (genomic). mouse globin MATURE mRNA hybridized to cloned gene (genomic).
4 mRNA Splicing rRNA and tRNA are also sometimes spliced; however, these are not the current topic. Splice sites are strongly conserved Shapiro and Senapathy examined 3700 splice sites. Immediately before 3' splice site is pyridine rich and free of AG dinucleotide. Invariant consensus is GU at 5' donor site and AG at 3' acceptor site. This is usually referred to as the GT/AG rule.
MAMMALLIAN EXON | INTRON | EXON 5’ AG GUAAGU YNCURAC-YnNAG G ’ | | | 5’ SPLICE SITE * 3’ SPLICE SITE YEAST EXON | INTRON | EXON 5’ GUAUGU UACUAA-YAG ’ | | | 5’ SPLICE SITE * 3’ SPLICE SITE
Splicing is a 2 step trans-esterification Figure 14.4 Transesterification 1. First the 5' transesterification occurs and it generates 2'-5' phosphodiester bond. The 2' attachment point is a 2' hydroxyl of an A nucleotide within the intron. This position is called the branch point. The branch point is nucleotides upstream of the 3' splice site. Transesterification 2. Second to occur is the 3' splice site cleavage, with simultaneous exon ligation. Intron leaves the complex as a lariat. The number of phophodiesters is conserved. No energy is lost or consumed.
Notice the 2' to 5' phosphodiestion bond at the branch point. Spliceosome does splicing This is a very large macromolecular complex. Spliceosomes are about 25 nm X 50 nm. It assembles on the mRNA. Assembly consumes ATP.
Weaver page 404
9 Sharp & coworkers L1----IVS----L2 intron is 231n DO is an antiSNURP sera ME is the control sera Panel C is a Southern blot of the 10% acrylamide 8M urea gel probed with a L1L2 fragment. 4% poly- acrylamide gel 8M urea 10% poly- acrylamide gel 8 M urea Very hard to see band
10 Thin layer chromatography to demonstrate that A is the branchpoint
RNase T1 cuts after guanylate residues. RNase T1 cuts only single stranded RNA. Is the branched nucleotide attached to the 5’ end of the intron?
Snurps snRNPs pronounced snurps –small nuclear ribonucleoprotein particle The particle contains –small nuclear RNAs = snRNAs –small nuclear ribonucleoproteins pg 407
5’ splice site also called the donor site 3’ splice site also called the acceptor site
16 Branchpoint Yeast consensus: UACUAAC Mammallian: U 47 NC 63 U 53 R 72 A 91 C 47 16
17 Importance of the branchpoint Figure th edition
Figure 14.12
Base pairing is requried but is it sufficient?
Clearly base pairing with U1 is not all that is required.
25 Recognition of mammalian pre- mRNA intron sequences by snRNPs
Spliceosome Cycle Fig 14.28
27 SR proteins Serine (S) and Arginine (R) rich proteins that help to identify exons Involved in alternative splicing 27
snRNAs U1 - recognition (bp) of the 5’ splice site (donor site). U2 - branch point recognition (bp) & bps to U6 snRNA U5 binds ends of exons U4 binds U6 and holds it untile U6 is needed in a splicing reaction U6 - bps to 5’ splice site and U2 snRNA & U4 snRNA 3’ splice site should be n downstream of branch point. Slu7 and U2AF use branch point to help recognize 3’ splice site.
Group II self splicing
Self splice and non-self splicing Group II mitochondria
Figure 14.22
Group I introns rRNA
34 RNAP II CTD Experiment: CTD-GST stimulates splicing in vitro. GST does not. CTD binds snRNPs and splicing proteins. 34
35 Exon definition - intron definition Intron definition is sufficient to identify ends of introns. –For some transcripts the splicing machinery identifies the ends of introns without help from CTD. Exon definition is needed to successfully identify the ends of introns –Here CTD helps to identify the ends of the EXONS. –These types of transcripts are not spliced if the exons are not whole. 35
Figure This topic begins on page 427.
39 U1 SNRP U1 SNRP U2SNRP U2AF U2SNRP U2AF SXL
40 Regulation of splicing Negative - SR protein binds and hides a required sequence Positive - a crummy sequence (eg branch point) is enhanced with the help of a protein (eg U2AF). 40
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