W3L1 Nuclear architecture and chromatic Flashcards

1
Q

Nuclear structure

A

The nucleus condensate
! Liquid-liquid phase separation
! Separation of nuclear components into non-membrane bound domains
! Condensate contain Low-complexity domains (LCDs) or intrinsically disordered regions (IDRs)
! Increase the local concentration of components required for transcription initiation

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2
Q

Nuclear organization

A

! The nucleus is not homogenous
! Position of genes can affect expression
-Nuclear scaffold
- Chromosome territories (more transcription in the middle, less to the periphery )
- Active and inactive

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3
Q

Sub nuclear localisation

A
  • the position of the gene in the nuclear might lead to expression or no expression
    -after a cell receive a signal, inactivate gene is then moved into the nuclear neighborhood for gene expression from the repressive domain in the lamia
    -location can affect expression but there are other factor and gene dependent
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4
Q

Chromsome structure and gene regulation

A

! Position of genes on chromosomes can affect expression
! Gene in Heterochromatin region– silenced (darker colour when stained)
!gene in Euchromatin – potentially active
-barrier prevent heterochromatin bleed into euchromatin, occur via DNA methylation
! Position effect variegation is when gene is inserted into the heterochromatin due to rare chromosome inversion

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5
Q

DNA methylation

A

-the process is gene dependenti
-in mammal, it occur at CpG doublet
! Two classes of DNA methylases
! De novo methylase which methylase un methylase strand
! Maintenance methylase which return the methylation pattern state of the newly produce strand (inheritable)
-DNA demethylase reverse the methylase state

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6
Q

DNA methylation and turning gene expression off

A
  • a naked DNA can still be express when it is bind by regulator
    -methylation occur on the naked gene due to binding of CpG
    -protein bind to the methylated DNA, regulatory factor cannot bind to it
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7
Q

Methylation and histone modification

A

-DNA methylation can affect the recruitment of histone modifying enzymes
- the histone modifying enzymes can affect DNA methylation, still allow for regulatory protein to bind

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8
Q

Histone type

A

! Core histones
! H1, H2A, H2B, H3 and H4
! Histone variants
! H2A.X, H2A.Z, CENPA, H5

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9
Q

Histone variants

A

-histone have different variant that have different histone fold

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10
Q

Arrangement of DNA and histone

A

-Not randomly distributed along DNA
Some position can look like random positioning, nucleoside free region, identical position in the population or having histone variant

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11
Q

Nucleosome free region

A

-We need binding sites for regulatory proteins
-nearby nucleosome contain H2A.Z which define a NFR

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12
Q

What is a driving factor behind nucleosome (histone dna ball) location

A

-DNA protein interaction
-nucleosome position can be directed, driven by DNA binding protein

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