RNA Processing Flashcards

1
Q

How many RNA polymerases are there in eukaryotes and what do they transcribe?

A

3
Pol I - rRNA (main)
Pol II - mRNA (main), snRNA, miRNA
Pol III - tRNA (main), 5S rRNA, other small RNAs

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

What are the different types of RNA processing?

A

Cleavage, Splicing, 5’ capping, polyadenlyation, base insertion, deletion, modification

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

What are 2 characteristics of rRNA genes in the genome?

A

Polycistronic messages and found repeated in all genomes.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

How are rRNAs primarily processed?

A

Through endo and exonucleolitic activities.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

List the 5 ways tRNAs are processed post-transcriptionally in eukaryotes?

A
  1. 5’ cleavage by RNase P
  2. 3’ cleavage by tRNase Z
  3. CCA is added to 3’ end by enzyme
  4. Post-transcriptional modifications of bases
  5. Intron excision
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

What are two common post-transcriptional modifications of rRNA in eukaryotes and which snoRNAs mediate those modifications?

A
  1. 2’ O methylation by box C/D snoRNA

2. Pseudouridylation by H/ACA snoRNA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

How do snoRNAs facilitate modification of nucleotides?

A

In a template driven manner. snoRNAs bind to complementary sequence and position nucleotide for modification within active site.

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

What is odd about the 5’ cap found on mRNAs?

A

The guanosine is attached to the first base in a 5’ -> 5’ linkage

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

What are the 3 steps involved in 5’ capping?

A

1) Removal of terminal phosphate from nascent RNA
2) Addition of GMP to the end, forming a 5’ -> 5’ linkage
3) Methylation of guanine

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

What binds to the poly A tail?

A

Poly A Binding Protein (PABP)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

What can be used to enrich mRNA transcripts from lysates and why is this significant?

A

Use Poly-A tail by pulling down with Poly-T oligos. only 3% of total cellular RNA is mRNA. Majority is rRNA

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

Which mRNAs do not have poly A tails and how do they get around this?

A

Histone mRNAs. Have a 3’ end stem loop generated by U7 snRNP-mediated interaction. Stem loop is bound by its own protein instead of PABP

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

5 roles for 5’ cap and poly A tail

A
  1. Help downstream maturation including splicing and transcription termination
  2. mRNA stability
  3. Facilitate transport to cytoplasm
  4. Important for translation initiation
  5. Alternative polyA/capping can be regulatory
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

What consensus sequences are recognized by the splicing machinery?

A

5’ splice site GU
3’ splice site AG
Branch point A
Purine Rich Sequence downstream branch point

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

Describe or draw the 3 steps of pre-mRNA splicing?

A

1) 2’ OH of branch point Adenosine attacks 5’ splice site
2) Free 3’ OH of exon attacks 3’ splice site.
3) Get lariat (2’5’) intermediate that’s degraded

Note: not energetically demanding

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

What is the main part of snRNPs that catalyze reactions? What is the theme associated with the spliceosome?

A

RNAs. The spliceosome isn’t a large machine that works all at once. It consists of smaller RNPs that dynamically lead to splicing.

17
Q

How do the mechanisms of Group I and Group II introns differ?

A

Group I introns use an exogenous guanosine to initiate attack 5’ splice site. Group II introns use branch point adenosine, similar to how introns are spliced in eukaryotes.

18
Q

What happens if you mutate the 5’ splice site of an intron in higher eukaryotes?

A

You get exon exclusion. Exons are defned in higher eukaryotes.

19
Q

What happens if you mutate the 5’ splice site of an intron in lower eukaryotes?

A

You get intron inclusion. Introns are “defined” in lower eukaryotes.

20
Q

How are the strengths of splice sites modulated in different tissues?

A

Differential expression of RNA binding proteins (such as intronic silencers) can change the splice site that will be used. This can cause proteins to be functional or non-functional trough alternative splicing.

21
Q

What is an example of RNA editing?

A

Nucleotide addition and deamination

22
Q

How is RNA canonically destroyed in eukaryotes?

A

PAPB disassociates and a 3’-5’ exonuclease / exosome cleaves one end.
Another enzyme decaps the mRNA and Xrn1 cleaves 5’->3’ with exonuclease.