Unit 2 - Transcription Flashcards

1
Q

RNA is transcribed from the

A

5’ to 3’ direction

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2
Q

UTR

A

Un-Translated Region

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3
Q

AUG

A

translation starts

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4
Q

Prokaryotic Initiation

A

Binding of RNApol, Promoter melting, Initial transcription

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5
Q

Prokaryotic Elongation

A

Conformational changes in RNApol, Start of transcription, Unwinding, elongation, & re-annealing

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6
Q

Prokaryotic Termination

A

Use of terminators, Stop & release of the RNA product.

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7
Q

Core polymerase

A

Unit in RNA pol that catalyzes RNA synthesis but cannot initiate elongation unless dissociated from subunit.

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8
Q

Sigma subunit

A

Unit in RNA pol that facilitates polymerase binding to DNA at -35 & -10 promoter elements

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9
Q

two important DNA sequences within the promoter in prokaryotes

A

10 and -35 elements are six nucleotides each, and are located either 10 or 35 base pairs upstream of the actual start site of transcription

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10
Q

release of sigma factor

A

RNA pol can start elongation process

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11
Q

The place at which RNA synthesis stops

A

termination signal, recognized by RNA pol.

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12
Q

rho-Independent termination

A

Utilizes a stem loop & UUUU (intrinsic sequence) on DNA sequence. No protein needed, hairpin (on RNA) disrupts RNApol and transcription is terminated.

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13
Q

rho-Dependent termination

A

requires a stem loop & rho protein. rho protein has an ATP-dependent helicase activity. Rho binds to its rho recognition site, moves along the RNA until it reaches the RNA pol that is paused at the termination site. Then rho will separate the RNA-DNA helix, releasing RNA.

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14
Q

Rifampicin

A

Used in treating tuberculosis (a.k.a., Dactinomycin). Action: Inhibits initiation of transcription by binding to the b subunit of prokaryotic RNA polymerase thus preventing growth.

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15
Q

Eukaryotic initiation

A

requires binding of specialized, general transcription factors and RNApol to promoter sites at the beginning of a gene.

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16
Q

Eukaryotic Elongation

A

requires local unwinding of DNA helix, includes synthesis of RNA transcript.

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17
Q

Eukaryotic Termination

A

not well characterized. Release of newly synthesized transcript

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18
Q

Eukaryotic Post-processing

A

5’ capping, 3’ poly-A tail addition, splicing.

19
Q

RNApol1

A

transcribes three major rRNAs

20
Q

RNApol2

A

transcribes mRNA

21
Q

RNApol3

A

transcribes tRNA (and small rRNA)

22
Q

TFIIs (A, B, D, E, and H)

A

required by RNApol II

23
Q

TFIID

A

Binds to the AT-rich promoter element called the TATA box, contains TATA-binding protein (TBP).

24
Q

TATA-binding protein (TBP)

A

functions much like the bacterial s factor in that it allows the TFIID complex to recognize and bind to the TATA box.

25
Q

TFIIH

A

a multisubunit protein complex that has two activities: Helicase activity, Kinase activity (phosphorylates the C-terminal domain (CTD) of RNApolII)

26
Q

When CTD is phosphorylated

A

CTD no longer binds to GTFs and GTFs are released, beginning enlongation.

27
Q

5’ “Capping”

A

The 5’ end of the pre-mRNA is modified by the addition of a 7-methylguanosine as soon as mRNA synthesis begins. provides stability to the RNA molecule by protecting it from degradation by nucleases. also plays an important role in positioning mRNA on the ribosome for initiation of translation.

28
Q

7-methylguanosine

A

a guanosine molecule that has been methylated (FYI, at position 7 of the purine ring)

29
Q

Purpose of the poly(A) tail

A

(i) required for stability of the mRNA; (ii) functions as a signal for export of the mRNA from the nucleus to the cytoplasm; (iii) efficient re-initiation of translation (interacts with 5’cap).

30
Q

protein coding sequences

A

Exons = “expressed regions”

31
Q

noncoding sequences

A

Introns = “intervening regions”

32
Q

pre-mRNAs

A

Not-yet-spliced mRNAs are called “primary transcripts” or pre-mRNAs, and contain both exons and introns.

33
Q

RNA Splicing : 5 Steps

A
  1. Cleavage at 5’ splice site. 2. Folding of intron mRNA into a lariat structure at the branch point. 3. Cleavage at the 3’ end. 4. Assembly of neighboring exons to form mature mRNA.5. Lariat degraded by nucleases.
34
Q

spliceosome

A

a complex composed of both protein and snRNA that excise introns and ligate (splice) exons.

35
Q

alternative splicing

A

The use of different patterns of splicing to give rise to different mRNA sequences ( and thus different protein products).

36
Q

always transcribe in the 5’ to 3’ direction

A

RNA polymerases

37
Q

does not need a primer

A

RNA polymerase

38
Q

Prokaryotic Transcription Initiation Complex

A

Holoenzyme

39
Q

Eukaryotic Transcription Initiation Complex

A

TFIID(TBP), General Transcription Factors, and RNA polymerase II

40
Q

Prokaryotic Start Sequence

A

35 and 10 promoter sequences

41
Q

Eukaryotic start sequence

A

(-10) TATA box

42
Q

Prokaryotic post-processing

A

None

43
Q

Eukaryotic post-processing

A

5’ 7-methylguanosine cap, Splicing, 3’ poly-A tail