Chromatin structure and histone code Flashcards

1
Q

what is chromatin?

A

chromosomes + associated proteins

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2
Q

what are the four levels of packaging?

A

1st : DNA + histones = nucleosomes
(beads on a string)

2nd : nucleosomes pack themselves into fibres of 30nm (solenoid)

3rd : 30nm fibres pack themselves into 80-1–nm fibres

4th : represented by the mitotic chromosomes

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3
Q

what do chromosomes consist of?

A
  • DNA
  • histone proteins
  • non-histones proteins
  • non-coding RNA
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4
Q

nucleosomes

A
  • histones assemble to form an OCTAMER
  • this is 2 molecules of each histones (H2A, H2B, H3 and H4) with the DNA molecule wrapped around the structure
  • the N-terminal tails of the histone proteins are +ve charged and stick out of the octamer structure
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5
Q

compaction of nucleosomes

A

compaction of nucleosomes occurs to form higher order structures which involves:

  • linker histones (H1) link together octamer cores (nucleosomes) to form a solenoid (30nm fibre)
  • packaging proteins bind to histones tails to bring them together
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6
Q

what are histone remodelling factors?

A
  • enzymes that remove and replace nucleosomes
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7
Q

euchromatin

A
  • lightly staining areas of chromatin
  • less DNA
  • rich in genes
  • made up of nucleosomes, but not dense higher order packaging (low order of packaging)
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8
Q

heterochromatin

A
  • darkly stained areas
  • more DNA
  • few genes (most of the DNA is “useless” to the specific cell)
  • dense higher order of packaging (has a lot of DNA to pack) of nucleosomes
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9
Q

facultative heterochromatin

A
  • contains genes that are not expressed in that cell type
  • DNA tightly packaged as heterochromatin
  • BUT it may be packaged as euchromatin in other cell types as other cell types may need to express those certain genes
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10
Q

what determines whether nucleosomes are packed as HETEROCHROMATIN or EUCHROMATIN?

A

the type of cell

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11
Q

constitutive heterochromatin

A
  • there is a section of heterochromatin that will NEVER become euchromatin as the cell will NEVER need those genes to be expressed
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12
Q

EXAMPLE: the production of a beard

A
  • pre-puberty, skin cells on the face will not express the genes for hair follicles, this gene will be packaged under the category of “FACULTATIVE heterochromatin”
  • post-puberty, chemicals (testosterone) will activate the genes for hair follicles and will therefore become euchromatin
  • this will change the heterochromatin to allow the expression of the hair follicles for a beard to grow
  • mashallah boys
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13
Q

what chemical modifications take place to convert heterochromatin to euchromatin and vice versa?

A
  • methylation —-> coverts euchromatin to heterochromatin

- acetylation ——> converts heterochromatin to euchromatin

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14
Q

what are the enzymes that allow chemical modification of histone tails to take place?

A
  • HAT –> histone acetyl transferase

- HMT –> histone methyl transferase

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15
Q

how does chemical modification occur?

-acetylation/methylation

A
  1. TF bind to DNA
  2. recruitment of histone modification enzymes (HAT/HMT) via N-CoA (nuclear coactivator)
  3. this leads to unpackaging of DNA
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16
Q

what is acetylation?

A
  • the loss of +ve charge from the histone tails
17
Q

what is methylation?

A
  • addition of a methyl group to DNA
18
Q

HATs

A
  • histone acetyl transferase
  • acetylate lysine residues (AA) on histones
  • leads to unpacking of chromatin
19
Q

HDACs

A
  • histone deacetylases
  • De-acetylate histones
  • lead to compaction of chromatin
20
Q

EXAMPLE : thyroid hormone receptors

A
  1. thyroid hormone receptor (TR) binds to the thyroid response element (TRE) on the DNA strand
  2. this recruits (HDAC/DM (de-methylase)) via the N-CoR (nuclear corepressor) which causes De-methylation
  3. Then we, recruit HAT and HMT via the N-CoA (nuclear coactivator), which then causes acetylation, so the DNA unwinds even more (making euchromatin).
  4. RNA Pol II binds and transcribes thyroid genes.
21
Q

nuclear co-repressor (N-CoR)

A

-aids in the recruitment of HDAC and DM to remove chemical groups from DNA

22
Q

nuclear co-activator (N-CoA)

A
  • aids in the recruitment of HMT and HAT to add chemical groups to DNA
23
Q

Histone modification via methylation

A
  • histone tails are methylated by histone methyl transferase (HMTs)
  • De-methylated by histone demethylase (HDMs)
  • a lysine residue can be mono, di or tri methylated
24
Q

Loops and chromatin domains

A

There is evidence that suggests
- Each loop may have a different degree of chromatin compaction
- The scaffold isolates the chromatin in one loop from the next loop
- So one loop may have open chromatin and active genes
The neighbouring loop could be tightly packed as heterochromatin

25
Q

Methods to investigate chromatin structure- DNAse digestion

A

DNAse I cuts double stranded DNA - HYPERSENSITIVE SITES (HSS). They are:

  • Sequences of DNA without histones
  • May be naked DNA, or binding transcription factors
  • Cut by very brief digestion with DNAse I
  • Found in promoters and enhancers

-Histone binding protects DNA from DNase digestion

26
Q

Marks for promoters and enhancers

A
  • Promoters strongly enriched for H3K4me3

- Active enhancers enriched for H3K4me1

27
Q

Histone code

A
  • Histone “marks” are read by binding proteins
  • Related domains are found in multiple code reading proteins e.g.
  • Bromodomain proteins bind to acetylated lysines
  • Tudor domain and chromodomain proteins read lysine methylation
28
Q

Examples of how methylation has varying effects.

A
  • Trimethylation of histone H3 lysine at position 9 (H3K9me3) associated with heterochromatin
  • Monomethylation of histone H3 lysine at position 9 (H3K9me1) usually associated with active chromatin