lec 8 Flashcards

(37 cards)

1
Q

are some genes transcribed all the time?

A

yes
- regardless of cell type/environmental conditions
- genes = “constitutive”

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2
Q

transcriptional regulation determines

A
  1. which genes are expressed
  2. when they are expressed
  3. degree (# of copies of RNA) that they are expressed
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3
Q

open reading frame (ORF)

A

region between translational start + stop/termination codons
- have introns and exons

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4
Q

what are the regulatory regions that influence each gene?

A
  1. promoter: upstream
  2. enhancer: may be up or downstream or in introns
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5
Q

transcription factors (TFs)

A
  1. determine if RNA Pol II gets recruited to gene
  2. affect the stability of RNA Pol I and transcription in initiation complex
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6
Q

what are the 2 types of transcription factors

A
  1. TFII (general TF)
    - expressed in every cell type
    - req for RNA Pol II to bind to the promoter
    - form a complex at the promoter and work together to recruit RNA Pol II
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7
Q

what is needed for transcription to occur?

A

RNA Pol II and TFIIs

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8
Q

promoter

A

binds transcription initiation complex

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9
Q

transcription initiation site

A

where RNA Pol starts making RNA transcript

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10
Q

transcription termination site

A

where transcription stops

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11
Q

exons

A

the region that codes for proteins
- exit the nucleus, are expressed

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12
Q

introns

A

will be removed from the transcript through splicing after transcription
- do not code for protein
- stay in the nucleus, excised via RNA splicing

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13
Q

translation termination codon

A

where translation stops

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14
Q

translation initiation codon

A

where translation of RNA into peptide begins

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15
Q

3’ and 5’ UTR

A

3’ and 5’ untranslated region
- not translated
- follows transcription
- proteins bind to regulate translation
- part of DNA and mRNA

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16
Q

tissue-specific transcription factors (TSTFs)

A
  1. req for transcription
  2. bind to enhancers
  3. do not have to be upstream
  4. bind to enhancer regions and have tissue and cell type-specific expression
  5. create binding sites for the TFII family
  6. help stabilize transcription initiation complex
17
Q

how do you think it is possible for an enhancer region to affect the recruitment of RNA Pol II and interact with TFIIs if it is located far away from the promoter

A

DNA can form a folded conformation
- not linear all the time

18
Q

can 1 gene have many enhancers?

A

yes
- enhancers bind to TSTFs
> different TSTFs = expressed in different cell types

19
Q

T/F TFIIs bind to enhancers

20
Q

T/F a gene can have many enhancers

21
Q

T/F neuron-specific enhancer DNA will be present in DNA of muscle cells

A

T, neurons TSTF will not be expressed

22
Q

T/F TFIIs are expressed in every cell type

23
Q

T/F TFII transcribes genes

A

F, req for transcription gene but RNA Pol II transcribes genes

24
Q

what is one of the contributors to cell specialization

A

differential gene expression

25
histone mods and epigenetics
epigenetic mechanisms = influence gene expression w/o affecting underlying DNA seq
26
what are 2 examples of histone mods and epigenetics
1. regulation of chromatin structures - how tightly or loosely packed 2. chemical mod of DNA - DNA methylation
27
transcription initiation
RNA Pol II TFIIs TSTF and enhancer
28
chromatin and nucelosome structure
DNA packaged with histone proteins = chromatin nucleosome = basic unit of chromatin - 1 histone octamer and wrapped DNA
29
histones and transcriptional regulation
covalent post-translational mod to histones affect the conformation of DNA - causing to be "open/uncondensed" or "closed/condensed" conformation
30
enzymatic mods of histones can influence what
where transcription machinery has access to enhancers and/or promoters
31
epigenetic change
change in chromatin/DNA structures that affect gene expression - does not affect the gene seq
32
histone acetylation
associated w/ active transcription open relaxed chromatin
33
histone methylation
context-dependent associated with activation and repression of transcription associated w/ DNA silencing
34
histone acetyl transferases (HATs)
acetylate N-terminal of histones - leads to relaxed chromatin > open/accessible to transcriptional machinery = more transcriptionally active adds acetyl groups
35
histone deacetylases (HDACs)
remove acetylene groups - leads to chromatin > more condensed = transcriptional repression
36
if HATs level increased, it is safe to say that the transcription would be active or repressed?
active
37
what do you expect would be the effect on the chromatin structure of applying HDACs inhibitor to cells?
it will loosen the chromatin