Lecture 3 final Flashcards

1
Q

What is the goal of bisulfide sequencing

A

chemical modification of cytosine to uracil in order to study DNA methylation

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2
Q

During Bisulfide sequencing, __________________________________ but those that are methylated are resistant to this modification and remain

A

cytosine to uracil

cytosine

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3
Q

What are the steps of bisulfide sequencing

A
  1. bisulfate treatment
  2. PCR amplification
  3. sequencing of genome
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4
Q

What are the analysis steps

A
  1. Align reads to known DNA

2. Determine methylated cytosine

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5
Q

What are the 4 steps of bisulfide analysis

A
  1. convert all genomic Cs to Ts in the reference genome
  2. Convert all Cs to Ts in the read was well (only As, Gs, and Ts in all sequencing)
  3. Align with regular aligners- C/T discrepancy is gone! Alignment is more accurant
  4. Compare sequence of the original reference genome and reads
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6
Q

Based on graph,

DNA methylation has a ________________ bias

A

3’ bias

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7
Q

_______________ are uniformly methylated

A

pseudogenes and non expressed genes

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8
Q

Expression of methylated Genes:
Body methylated genes tend to have higher than average expression. Promotor methylated genes tend to have __________________

A

lower expression

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9
Q

Promotor methylated genes tend to have _____________

A

tissue specific expression

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10
Q

What are the two types of Chromatin?

A
  • Euchromatin

- Heterochromatin

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11
Q

What are the qualities of euchromatin?

A
  • Less dense appearance in EM
  • enriched with acetylated histones and there positive chromatin modifications
  • permissive transcription
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12
Q

What are the qualities of heterochromatin?

A
  • Dense appearance in EM
  • Enrichment in hypoacetylated histones and negative chromatin modification
  • non permissive for transcription
  • formation of chromosomal structures
  • chrommers and temoers
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13
Q

What is the function of Histones

A

Compacting DNA strands and regulation of gene expression

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14
Q

Histones are highly basic proteins abundant in ____________________ residues that are found in eukaryotic cell nuclei

A

Lysine and arginine

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15
Q

What are the 5 classes of histones

A
  • Core: H2A, H2B, H3, H4

- Linkage: H1/4

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16
Q

What are the functional units of chromatin

A

nucleosomes

17
Q

Histones are positively charged which allowed them to associate with DNA which is ______________

A

negatively charged

18
Q

Histones undergo post translational modification which alter their _____________

A

interaction with DNA and nuclear proteins

19
Q

How do you name a histone

A
  1. Name of histone
  2. Single letter abbreviation of amino acid and position
  3. Type of modification
20
Q

Euchromatin is accurate with ____________

A

activation

21
Q

How does histone activation promotes transcription?

A

A bromodomain (BD) is protein domain that recognizes acylated lysine residues such was this on the N terminal tail of histones

22
Q

Coding in histones may be ____________

23
Q

Generally:

Histone activation is associated with ________________

A

transcriptionally active genes

24
Q

Generally:

Histone deaccetylation is associated with

A

deactivation

25
How to study histone medications: development and usage of _______________
histone modification specific antibodies | Ex: Western blot; immunoflourescnce, chromatin immunoprecipation (CHIP) assays
26
______________ is useful for extraneous the enrichment of specific histone modification or binding of specific factors to the gene of intrest in vivo
CHIP assay
27
What are the steps of CHIP assay
1. DNA protein crosslinking 2. Chromatin isolation 3. Immunoprecipation (IP) 4. Find out what these sequences are
28
After the DNA associated with the complex is purified to find out what DNA sequences are associated with the modification histone:
- PCR - Microarrays - CHiip seq **Chiip seq discussed later
29
______________ shows the absolute fragment counts shown. Isolated peaks show where the protein has bound in the data
chip-seq
30
________________ in embryonic stem cells.
Distinct histone modification pattern
31
Differential cells contain either __________________ but not both
repressive or active markers
32
Hypothesis bivalent domain silence developmental genes in ________ them posed for activation later
ES cells
33
Epigenetic changes are common in ____________
epigenetic diseases
34
Turning the clock back on epigenetic diseases. ______________
epigenetic therapies are effective because
35
Epigenetic changes are ____________
reversible
36
Epigenetic changes do not normally associate with __________
genetic mutations
37
_____________ can be used to turn genes on or off
epigenetic therapies