Lecture 12. Eukaryotic Transcription Flashcards

1
Q

Where does bacterial transcription and translation?

A

In the same compartment

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2
Q

Where are eukaryotic transcripts transported to?

A

Cytosol

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3
Q

Where are the mRNA precursors processed?

A

In the nucleus

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4
Q

What does eukaryotic RNA polymerase require?

A

General transcription factors

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5
Q

Conserved elements of eukaryotic RNA Polymerase II promoters

A

Inr
TATA box
DPE
Enhancer

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6
Q

Inr

A

Initiator element

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7
Q

TATA box promoter

A

Contains a TATA box: The upstream sequence TATAAAA usually between -30 and -100 from transcriptional start

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8
Q

TATA-less promoter

A

Downstream core promoter element between +28 and +32 from transcriptional start

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9
Q

Enhancer

A

Can be several kb away

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10
Q

Similarities between bacterial and eukaryotic replication mechanisms

A

NONE - fundamentally different RNA replication mechanisms

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11
Q

What guides RNA Pol II to its promoters?

A

TFIID

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12
Q

What does bound TBP act as in initiation?

A

A nucleus for further recruitment

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13
Q

What is TFIIH?

A

A helicase that opens the DNA double helix and a kinase that phosphorylates the C’ - terminal domain of the RNA Pol II L’ subunit

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14
Q

Elongation process

A
  1. TFIIB, E and H dissociate from the basal transcription apparatus
  2. RNA is synthesised
  3. RNA Pol II progresses, freeing the promoter and TFIID/A complex for further recruitment
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15
Q

What is a potent inhibitor of RNA polymerase II

A

α-amanitin

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16
Q

What do enhancers do?

A

They increase the transcriptional levels of ges

17
Q

The DNA looping model

A

Proteins bound to a distant enhance interact with components of the transcription initiation complex, thus looping out the intervening DNA

18
Q

What does the mediator protein do in the DNA looping model?

A

Act as a bridge between activator proteins that bind the enhancer control elements and the non-phosphorylated CTD of RNA Pol II in its initiator state

19
Q

In what three ways are the RNA Pol II transcripts (mRNAs) modified?

A
  1. The 5’ end is capped by a nucleotide triphosphate through an unusual linkage. The process is accompanied by methylation
  2. The 3’ end of the primary transcript is trimmed and a poly-A tail is added
  3. Introns are removed by splicing