Lecture 10 - RNA Processing_final Flashcards

(33 cards)

1
Q

What are constitutive exons?

A

Present in every transcript

Constitutive exons are essential components of mature mRNA.

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2
Q

What are cassette exons?

A

Choose only one of the group

Cassette exons contribute to alternative splicing variations.

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3
Q

What is the lariat structure in splicing?

A

Branched structure of an excised intron

The lariat is formed during the splicing process.

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4
Q

What type of bond is formed during the splicing reaction?

A

2’-5’ phosphodiester bond

This bond links the branch site to the intron.

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5
Q

What is the role of splice sites?

A

Serve as recognition signals to the splicing machinery

These sequences are conserved in all eukaryotes.

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6
Q

True or false: Mutations in splice site sequences generally enhance splicing.

A

FALSE

Mutations typically abolish splicing efficiency.

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7
Q

What is the function of the spliceosome?

A

Removes introns from pre-mRNA

The spliceosome is composed of snRNPs and proteins.

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8
Q

What do snRNPs contain?

A
  • One snRNA
  • 7-15 proteins

snRNPs are essential for the formation of a catalytically active spliceosome.

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9
Q

What is the catalytic site of the spliceosome primarily formed by?

A

RNAs, not by proteins

This distinguishes spliceosomes from ribosomes.

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10
Q

What are the two recognition factors in splicing?

A
  • U1: finds the 5’ splice site
  • U2: finds the branch site

These factors are crucial for spliceosome assembly.

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11
Q

What happens in the first reaction of pre-mRNA splicing?

A
  • Bond between last nucleotide of exon 1 and first nucleotide of intron is broken
  • New 2’-5’ bond is formed

This reaction initiates the splicing process.

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12
Q

What occurs in the second reaction of pre-mRNA splicing?

A
  • Bond between last nucleotide of intron and first nucleotide of exon 2 is broken
  • New 3’-5’ bond is formed

This completes the splicing process, releasing the intron.

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13
Q

What is the significance of alternative splicing?

A

Allows the proteome to be bigger than the genome

This process generates protein isoforms that can modulate function.

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14
Q

What are Group I introns known for?

A

Self-splicing RNAs

They fold into a catalytically active structure.

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15
Q

What distinguishes Group II introns from Group I introns?

A

Closely resemble pre-mRNA introns

They use a similar two-step mechanism for splicing.

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16
Q

What is the role of maturases in splicing?

A

Enhance the rate of splicing

Maturases are proteins that assist in the splicing process.

17
Q

What is the function of the 5’ cap in mRNA?

A

Protects the 5’ end from nucleases

The cap is crucial for mRNA stability and translation.

18
Q

What does the poly(A) tail do?

A

Protects the 3’ end from nucleases

It regulates the half-life of mRNA in the cytoplasm.

19
Q

What is the significance of RNA processing in eukaryotes?

A

Eukaryotic mRNAs undergo many processing steps

This includes capping, polyadenylation, and splicing.

20
Q

What are the two components required for efficient translation of an mRNA?

A
  • Cap
  • Poly(A) tail

Both components communicate with each other during the translation process.

21
Q

The largest subunit of RNA polymerase II has a long ________ tail.

A

carboxy-terminal

This tail must be unphosphorylated for Pol II to initiate transcription.

22
Q

What enzyme phosphorylates the amino acids on the carboxy-terminal tail of RNA polymerase II?

A

TFIIH

Phosphorylation by TFIIH allows Pol II to release from the initiation complex.

23
Q

What are the two ends of eukaryotic mRNAs formed during processing?

A
  • 5’ cap
  • 3’ poly(A) tail

These modifications are crucial for mRNA stability and translation.

24
Q

What process involves the removal of introns from RNAs?

A

Splicing

This process links exons together to form mature mRNA.

25
Name the **three different splicing mechanisms** identified.
* Group I intron splicing * Group II intron splicing * Spliceosome ## Footnote All mechanisms involve the removal of intron RNA.
26
What structure protects the **5’ end** of an mRNA?
Cap structure ## Footnote A single non-templated G residue is added to the 5’ end of the pre-mRNA.
27
What enzyme adds GMP in an unusual **5’-5’ triphosphate linkage**?
Guanylyl transferase ## Footnote This enzyme is involved in the capping process of mRNA.
28
What do **methyl transferases** do to the G added to the 5’ end of pre-mRNA?
Add one or more methyl groups ## Footnote This modification is part of the capping process.
29
What are the **polyadenylation factors** that ride along on the phosphorylated carboxy-terminal tail of RNA polymerase II?
* CPSF * CStF ## Footnote CPSF stands for cleavage and polyadenylation specificity factor, while CStF stands for cleavage stimulation factor.
30
What directs **cleavage and polyadenylation** near the 3’ end of the pre-mRNA?
Polyadenylation signal ## Footnote This signal is encoded in the DNA.
31
What is the first step in **mRNA processing**?
5’ capping ## Footnote Caps are added to pol II transcripts shortly after initiation.
32
When does the capping process begin during mRNA processing?
When the nascent pre-mRNA is about 25 nucleotides long ## Footnote Capping enzymes ride along on the phosphorylated tail of the pol II large subunit.
33
What type of linkage is used when the G is put on the 5’ end of mRNA?
5’-5’ linkage ## Footnote This is referred to as a 'backwards' linkage.