Lecture 22: RNA Processign II Flashcards
Branch Point
At the region where the S2 small nuclear RNA base pairs and the A residue stick out due to skipping
Mutation in Intron that modifies nucleotide around splice site
Altering residue near 5’ end of intron stops the splicing
Splicesome
Once U2 and U1 bound to its corresponding intron splice site and branch point , it recruits U4//6//5 and the brings both ends close to one another so size doesn’t matter. Then U1 and U4 kicked off so the complex ends can be close together
Energy Expenditure During Splicing
Net 0
Debranching enzyme
Breaks the bond at branch point and then it gets degraded rapidly
Self Splicing Type 1
No splice some because secondary structure naturally brings them together and is common in plants
Absence of GU…..AG
AU……..AC 1% human introns. require different snRNPs because they need to match the base bair with different snRNAs
Trans-splicing
can do it on different molecule and no lariat forms just two introns (C. elegans)
Ribosomal rRNA synthesis (pol ?)
Pol I
In the nucleolus
Ribosomal RNA Processing
Pre-rRNAs are modified:
- Ribose methylation and conversion of U to pseudouridine
- Modification sites are determined by base pairing with snoRNAs that associate with modifying enzymes in RNPs
snoRNAs
Form a weird double hairpin with some single stranded ran in the middle so that it can be bound
tRNA pol?
Polym III
tRNA processing
Cleave sequence on 5’
CCA added to 3’
Extensive modification of internal base
Exonic Splicing Enhancers
SR proteins which bind to sites in exon interact with U1 because they interact with one another telling the U1 this is a site
3’ intron identification
U2AF65 and 35 bind to the U2 to tell them where the site is to cleave