W3L1 Nuclear architecture and chromatic Flashcards
Nuclear structure
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
Nuclear organization
! 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
Sub nuclear localisation
- 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
Chromsome structure and gene regulation
! 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
DNA methylation
-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
DNA methylation and turning gene expression off
- 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
Methylation and histone modification
-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
Histone type
! Core histones
! H1, H2A, H2B, H3 and H4
! Histone variants
! H2A.X, H2A.Z, CENPA, H5
Histone variants
-histone have different variant that have different histone fold
Arrangement of DNA and histone
-Not randomly distributed along DNA
Some position can look like random positioning, nucleoside free region, identical position in the population or having histone variant
Nucleosome free region
-We need binding sites for regulatory proteins
-nearby nucleosome contain H2A.Z which define a NFR
What is a driving factor behind nucleosome (histone dna ball) location
-DNA protein interaction
-nucleosome position can be directed, driven by DNA binding protein