Chromosome biology Flashcards

1
Q

what percentage of solid tumour cells have aneuploidy?

A

up to 90%

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
2
Q

what are the three levels in the heirachial organisation of interphase chromatin

A

topologically associating domains (TADs), compartments, chromosome territories

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
3
Q

what are TADs?

Topologically associated domains

A

fundamental units of three-dimensional (3D) nuclear organization
within compartments, big loops of chromatin that contain functional domains.

TADs move between compartments depending if they’re active or inactive

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
4
Q

what are compartments?

A

chromosome territories are divided into compartments that are either silent or active

active is wher transcription is going on

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
5
Q

what are the fundamental parts of a chromatin loop in interphase?

and what is their function in the loop?

A

Cohesin - complex that holds the DNA strands together forming the loop
CTCF - a protein that binds specific DNA sequences (CTCF motifs), which are positioned in the same direction. hence CTCF defines the size of the loop

Loop boundaries - involve cohesin and ctcf only during interphase

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
6
Q

In what ways do interphase and mitotic chromatin loops differ?

give three

A

size of loops
attachment sites
proteins involved in loop formation

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
7
Q

how do long distance interactions regulate gene expression

A

looping of chromatin allows for interactions between distant regions of DNA and regulatory complexes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
8
Q

give 4 ways in which disruption of elements that regulate chromatin organisation contribute/lead to cancerigenesis

A
  1. CTCF mutation or abnormal levels
  2. CTCF/cohesin binding sites are mutated
  3. breaking down of the TAD border structure (leading to de-regulation of gene expression)
  4. Pertubation of insulated neighbourhoods’ boundaries
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
9
Q

what happens when ctcf binding domins are methylated?

A

disrupts healthy neighbourhoods and allows other interations that can trigger transcription of genes that are normally silenced

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
10
Q

what are insulated neighbourhoods and why are they organised in this way?

A

Insulated neighborhoods are loops formed by the interaction of CTCF/cohesin-bound anchors containing genes and their regulatory elements
All the loops in insulated neighbourhoods, define domains of similar activity, within the insulated neighbourhood genes are either active or inactive, a way of isolating the domain from other factors

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
11
Q

what mutational changes can convert a proto-oncogene to an oncogene

A

nucleotide substitution (KRAS, EGFR, BRAF)
gene fusion (BCR-ABL)
enhancer hijacking (IgH-MYC)
focal amplification (MYCN, EGFR)
disruption of insulated neighbourhoods

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
12
Q

where is the most condensed form of chromatin found?

A

In mitotic chromsomes
(length up to 10000 shorter than naked state)

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
13
Q

what do readers do?

A

they bind specificallu to modified histones
usually bringing new activity to the vacinity of a modifed histone or alter the structure of the chromatin simply by binding to a histone mark

Some PTMs attract defined ‘readers’ to promote certain outcomes

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
14
Q

translation of a histone modification into biological function involves what 4 things

A
  1. Writers (enzymes) that are responsible for modifying histones
  2. Readers (binders) that recognise and interact with modified histones
  3. Sometimes effectors are needed, usually enzymes that change the status of chromatin to ‘close’ or ‘open’. Some readers may also do this
  4. Erasers (enzymes) that remove the modification

For the histone code to work properly, all these proteins must be present at appropriate levels

How well did you know this?
1
Not at all
2
3
4
5
Perfectly
15
Q

what are the three main epigenetic processes?

A
  • DNA methylation
  • Histone modification
  • Non coding RNAs
How well did you know this?
1
Not at all
2
3
4
5
Perfectly
16
Q

how does misregulated epigenetic control lead to cancer formation?

A

HDACs responsible for gene silencing and transcriptional repression - can occur in tumour suppressor genes
Histone acetylation at gene promoter and enhancers can promote transcription in oncogenes
Oncohistones are frequently mutated histones that are associated with tumourigenesis (H3K27M pediatric gliomas)
there are tumour promoting and tumour suppressive types of non coding rnas

DNA methylation is associated with resistance
hypermethylation at genes may lead of activation of oncogenes (DLX1)
methylation at promoter can repress tumour suppressor genes (eg P53, BRCA1)

17
Q

why is the histone code important in cancer biology?

A

many components of the histone code are mutated in cancer

18
Q

give some mutations in the histone code that are related to tumour growth

A

macroH2A
CENP-A/HJURP
ATRX/DAXX

19
Q

give some mutation in the histone code that lead to invasion or metastasis

A

H3.3
macroH2A

20
Q

give two examples of DNMT inhibitors

A

Decitabine
Hydralazine

21
Q

give two examples of HDAC inhibitors

A

valproic acid
suramin

22
Q

give two examples of HMT inhibitors

A

TCP
Pinometostat

23
Q

How can we repair epigenetic components in the treatment of cancer?

A

By using small drug inhibitors it is possible to restore normal combination of PTMs on histone which may in turn help to get rid of cancer