5. transcription Flashcards

(33 cards)

1
Q

gene expression

A

the process by which information from a gene is used in the synthesis of a functional product

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2
Q

main types of non-coding RNA

A
  • Protein translation: ribosomal (rRNA), transfer (tRNA)
  • RNA processing: small nuclear (snRNA), small nucleolar (snoRNA)
  • regulatory: micro (miRNA), long non-coding (lncRNA)
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3
Q

importance of control of gene expression

A
  • development and specialisation
  • prevention of cancer
  • adaption to environment
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4
Q

controlled points of gene expression

A

transcription
- measured by RNA-seq and qPCR
Co-transcription/mRNA
- alternative splicing
Post-transcription
- miRNAs
Post-translation

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5
Q

RNA pol II subunits

A

called Rpb#
- catalytic subunits (Rpb1 & Rpb2) p

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6
Q

main CTD residues to get phosphorylated

A
  • Ser 2 and Ser 5
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7
Q

Phosphorylation and de-phosphorylation enzymes

A

kinases - add phosphate group
phosphatase - remove phosphate group

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8
Q

RNA pol II needs help

A
  • recognising start (TSS or core promoter) or end gene on its own
  • binding DNA
  • remodelling histones
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9
Q

writer proteins

A

Add histone tail modifications

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10
Q

eraser proteins

A

remove histone tail modifications

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11
Q

reader proteins

A

recognises histone tail modifications

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12
Q

stages of transcription

A
  • pol II recruitment
  • initiation and early elongation
  • productive elongation
  • termination
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13
Q

pre-mRNA

A
  • virtual molecule
  • processing is co-transcriptional
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14
Q

Transcription start site (TSS)

A
  • the nucleotide where transcription starts at the 5’ nucleotide at the transcript
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15
Q

Core promoter (CP)

A
  • Where RNA Pol II is recruited to
  • close to/overlaps TSS
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16
Q

Cis-regulatory elements (CRE)

A
  • short DNA sequences (motifs) involved in transcriptional regulation
  • incudes enhancers and silencers
  • protein binding sites
17
Q

Transcription activators

A

transcription factors that recognise and bind a specific enhancer to initiate/increase transcription of target genes

two domains
- dna binding domain (DBD)
- Activator domain (AD)

18
Q

transcription repressors

A

transcription factors that recognise and bind specific silencer to prevent/repress transcription of target genes

two domains
- DNA binding domain (DBD)
- Repressor domain

19
Q

DNA activator/repressor binding domain

A

-Binds a silencer/enhancer
- holds repression/activation domain in promoter vicinity

20
Q

Activator activation domain

A

protein-protein interactions
- other activators (complex)
- co-activators

21
Q

Repressor repression domain

A

protein-protein interactions
- co-repressors
not present in every repressor

22
Q

stages of initiation and early elongation

A

-PIC formation/RNA pol II recruitment
- initiation
- abortive elongation
- promoter clearance

23
Q

spliceosome

A

is an ATP dependant complex of splicing factors that catalyzes mRNA splicing

24
Q

CTD phosphorylation during transcription

A
  • RNA pol recruitment : not phosphorylated
  • initiation and early initiation: Ser 5 P
  • Productive elongation : Ser 2 P, Ser 5 P
  • Termination: Both P removed -> no P
25
RNAPII Cleft
- contains helicase - unwinds DNA - opens transcription bubble
26
RNAPII wall
directs template strand into active site
27
RNAPII active site
- contains port for NTP entry - template faces pore and base pairs when the correct NTP enters - new phosphodiester bond catalysed
28
RNAPII bridge
- helps RNAP keep moving to the next base continuously
29
RNAPII DNA/RNA hybrid helix
- holds RNAP in place - important for stability
30
RNAPII rudder
- seperates DNA/RNA hybrid helix
31
PIC Formation
- transcription activators recruited - coactivators recruited - chromatin remodelling - TFIID recruited - other TFII# recruited - RNAP recruited
32
Co-activators
- protein-protein interactions - acetylate H3 and H4 - methylate specific histone tail residues
33
Nucleosome remodelling
Remodellers are recruited by - Histone tail mods (H3/4 acetylation and specific residue methylation) - interactions with proteins and activators They slide or evict nucleosomes - leave H3 and H4 - remove H2A/H2B dimmers