gene expression and control Flashcards

1
Q

define transciption factors

A

proteins that bind to cis acting elements of a gene

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2
Q

general vs cell/tissue specific TFs

A

general: minimum TF required for transcription
cell/tissue specific: regulate transcription of unique sets of genes in those cells/tissues

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3
Q

why do all cells of the individual have the same DNA

A

DNA from zygote is replicated many times with high fidelity

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4
Q

what genes are expressed in nearly all cells

A

housekeeping genes such as RNA/DNA pol coding genes, ribosome coding genes etc

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5
Q

define differentiation and what it is marked and preceded by

A

expression of appropriate subset of genes to carry out specialised functions
marked by a change in cell morphology, preceded by rapid proliferation

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6
Q

levels of gene expression regulation

A
  • chromatin accessibility
    (modify histones, chromatin remodelling, DNA methylation)
  • transcription regulation
  • mRNA processing
  • mRNA transport, localisation, stability
  • translation
  • post-translational modification
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7
Q

how does acetylation increase accessibility

A

negative acetyl group neutralises positively charged lysine and arginine, DNA less tightly bound, more accessible

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8
Q

what enzymes adds and removes acetyl group to histones

A

acetyl transferase, histone deacetylase

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9
Q

define histone code, how its maintained

A

distinct set of modifications to histone tails
preserved during DNA replication because its copied by proteins from parental histones to newly synthesised histones during chromosome replication

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10
Q

why is histone code important

A

proper gene expression, DNA repair, differentiation, prevents cancers and disorders

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11
Q

how are transcriptional activators and suppressors triggered

A

cell signalling due to cellular/environmental cues so body can adapt to changing conditions

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12
Q

what is SWI/SNF and what does it do

A

it is an ATP dependent chromatin remodelling protein complex
- pushes DNA around nucleosomes
- ejects histomes/octamers to expose TATA box
- remains bound in decondensed region for continuous gene expression

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13
Q

DNA methylation and CpG islands

A

CpG islands are regions with many C-G pairs
methyl groups are added to Cs in CpG islands, decrease accessibility and expression

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14
Q

fragile X syndrome and methylation

A

syndrome that results in in-vitro breaks on X chromosome
due to excessive (CGG)n repeats in UTR of X chromosome
causes methylation even when its not supposed to

number of repeats influences amount of methylation which influences severity of disease

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15
Q

how do general and specific TFs control transcription

A

general: control and are needed for initiation of transcription
specific: controls rate of initiation of transcription
specific TF bind their alpha helixes to the specific cis acting element in the DNA

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16
Q

transcriptional activators and supressors function

A

both are TFs
activators/suppressors bind to enhancer or promotor or repressor regions of the gene, increase/decrease recruitment of TFs and RNA pol to gene, increase/decrease gene expression

17
Q

how do general TFs, transcriptional activators and architectural proteins work together

A
  • TBP binds to TATA box etc
  • transcription activators (type of TF) binds to enhancers
  • architectural proteins bend the DNA
  • DNA and TF complex at enhancer loops to interact with TATA factors and architectural proteins, which increase rate of transcription initiation
18
Q

what is cooperative binding

A

when many different types of TFs bind and interact together, conformational changes occur, gene control options have increased
(e.g. 2 during transcription initiation, after TBP binds, other TFs can bind on because TBP serves as a base)

19
Q

what is combinatorial control of gene expression and what does it depend on

A

control of transcription rate due to combinations of TFs binding to promotors and enhancers
- DNA sequences present
- TFs present
- interactions between these TFs (eg through cooperative binding)

20
Q

functional domains function

A
  • part of TFs that recognise and bind to DNA promotor/enhancer
  • interacts with initiation complex
  • influences chromatin remodelling
  • sensor for internal/external cellular conditions
21
Q

3 ways that RNA processing contribute to gene expression

A

need 5’ cap and 3’ tail or else RNA pol will not recognise mRNA and gene will not be translated and expressed
secondary structure of mRNA must be removed by RNA processing for RNA pol to bind
alternative splicing means many proteins can be translated and hence expressed from 1 gene

22
Q

what must happen before RNA is exported

A

all RNA processing is finished and left over or damaged RNA has been degraded by exonucleases

23
Q

3 mechanisms for mRNA localisation

A
  • direct transport on cytoskeleton
  • random diffusion and trapping
  • generalised degradation and local protection
24
Q

anchor proteins function

A

bind to mRNA and make sure mRNA stays localised during translation

25
cytoskeleton role in mRNA transport
intermediate filaments and microtubles have distinct polarities (eg north and south poles), leading to asymmetry of cytoskeletal elements asymmetry provides direction for mRNA transport, along with signals from 3' UTR
26
cytoskeleton role in making sure daughter cells have different amounts of regulatory proteins
- cytoskeleton transports mRNA that codes for TFs to a localised spot with anchor proteins (e.g. left of the cell) based on instructions on 3' UTR - mRNA gets translated and produces TFs - TFs are closest to the left of the cell, concentration gradient of TFs exist, some TFs diffuse to the right - mitosis occurs, left daughter cell has more TFs than right one, both daughter cells will have different epigenetics
27
important of mRNA half life for gene expression
longer half life, more stable, more proteins can be made, gene is expressed more
28
2 mechanisms for mRNA decay
both start with nuclease shortening poly-A tail - slowly continues decaying from 3' to 5' - or 5' cap removed, rapid decay from 5' to 3'
29
what must occur before translation initiation (link to RNA processing)
mRNA secondary strucutre removed by translational eIF random extra proteins must also be removed translational eIF also checks 3' tail and 5' cap before translating
30
types of post translational modification
acetylation methylation lipidation disulphide bond phosphorylation glycosylation ubiquitination