Gene Expression Regulation II Flashcards

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1
Q

List 3 characteristics of gene expression regulation in eukaryotes

A

Gene regulatory proteins can act from a v.large distance from their promoters, RNA polymerase II doesn’t bind to promoter spontaneous it needs promoters (general transcription factors), and there is specific packaging of DNA(into chromatin)

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2
Q

Transcriptional activators bind to? Transcriptional repressors bind to ? They are capable of?

A
  • enhancers
  • silencers
  • they can act at a great distance, they can be localized up and down stream, they can act independently to their orientation
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3
Q

How do transcriptional activators work

A

They can act directly on transcriptional machinery(by increasing the affinity of RNA polymerase for the promoter and facilitating promoter clearance) or change chromatin structure around the promoter(by recruiting additional proteins or controlling the open/close state of chromatin)

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4
Q

What is transcriptional synergy

A

It is the effect of the binding of many transcription factors to the mediator resulting in many more transcribed sequnces

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5
Q

How can you control the state of chromatin?

A

The promoter is very near the TATA box, a gene activator protein attracts a chromatin remodelling complex and this makes the promoter more accessible for the RNA polymerase II, they can also change histones with other histomes that promote transcription, and recruit histones modifying enzymes (histones acetyl transferases) that promote gene expression

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6
Q

How do transcriptional repressors work

A

They can act on chromatin (form heterochromatin), and they can act locally (repress a specific gene)

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7
Q

What are some characteristics of transcriptional repressors

A

There is no direct competition for the promoter, the binding sites of activators and repressors are v.close so if one is bound the other cannot, if the both the repressor and activator are bound then the repressor can block the activator site of the activator,

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8
Q

How do transcriptional repressors work

A

They can recruit chromatin remodling complexes that help condensation of DNA, and have histones deacytylase

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9
Q

What are transcription foci

A

Are areas in the nucleus where gene expression is v.high, this is called a transcription factory such as the nucleolus, producing rRNA, here are the nucleoplasmic factories

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10
Q

What are insulators

A

They are elements that delimit an area of a gene that must be expressed, inhibit the spread of heterochromatin, block enhancers elements when They are between enhancer and promoter

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11
Q

What are epigenetic processes

A

They do not change sequences of bases but they affect structure of DNA, include processes like DNA methylation, histones modification, RNA mediated phenomena

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12
Q

How does DNA methylation occur

A

It is catalysed by DNA methyl transferase and it uses the methyl group of an intermediate called S-adenosylmethionine and releases it as S-adenosylmonocystine

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13
Q

Detail CpG islands

A

Are regions in the genome where the frequency of CG are normal whereas everywhere else CG is very low, they have become CpT, they are unmethylated and surround the promoter of house keeping genes, in order to have a CpT a germ line mutation must occur. there are 20000 CG islands, they are mostly on the 5’ end

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14
Q

How is methylation passed on

A

When DNA is replicated you have a Hemimethylated situation where one strand is methylated(parent) and one strand isn’t, now maintenance methylases add methyl groups to the new strand as they recognise the Hemimethylated sequences,

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15
Q

What are de novo methylases (de novo methyltransferases)

A

When a gene that used to be expressed need no longer be transcribed we use de novo methylases to methylate/inactive them

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16
Q

What is the purpose of DNA methylation

A

To keep genes silenced, to silence transposomes, to help genome imprinting (determination of gene expression based on parental origin), and for inactivation of an X chromosome in a female

17
Q

What is a nucleosome and it’s components

A

It is formed by 146 base pairs around a histone octamer whereas the tails (the aminoportion of the histone) are modified by acetylation, ,methylation, ubiquitylation, phosphorylation. Note that the changes are mostly in H3 ad H4 tetramer

18
Q

how is it decided which X is inactivated in females

A

it is random thus all females are a mosaic , this is shown in calico cats

19
Q

addition of an acetyl group onto a histone tail causes

A

it removes the positive charge of the Lys present in the histone tail, the histones are less tightly bound to DNA, chromatin is less compact, transcription of associated gene is favored

20
Q

what enzymes are associated with histone tail modifications

A

~histone acetyl transferases
~histone deacetylases
~histone methyl transferases
~histone demethylases