Epigenetics Flashcards
H3K4 methylation
H3K4 can be mono/di/trimethylated
associated with permissive active conformation
H3K27 Trimethylation
Repressive conformation of chromatin
H3K36 trimethylation
actively transcribed coding regions
Trithorax
complex responsible for for H3K4 methylation (active)
Catalytic subunit: MLL (methyltransferase)
Polycomb complex
Complex responsible for H3K27 methylation (repressive)
Catalytic subunit: Ezh2 (methyltransferase)
Demethylases
LSD1 and JumonjiC proteins erase the marks left by polycomb and trithorax
Poised chromatin
intermediate between active and silent
Defining marks
-null histone marks
-bivalent chromatin: both active and repressive marks
(these marks apply for noncoding RNA)
Histone acetylation
added by HAT removed by HDACs.
Acetylated chromatin classically viewed as active while deacetylation is repressive
may be more complicated than that
Canonical histones
H2A, H2B, H3 and H4
CpG methylation
Represses transcription when introduced in promoters
non CG methylation
non CG methylcytosine is associated with the gene-body region (usually in ES cells)
DNMT1
DNA methyltransferase
5-hydroxymethylation
5hmC is at transcribed regions, TSS, and some enhancer regions
-Generated by conversion of 5-mC to 5hMC
new epigenetic mechanism crucial for regulating pluripotency and the differentiation of ES cells and HSCs
TET proteins
Ten eleven Translocation proteins that convert 5mC to 5 hmC
Nucleosome positioning
localization of individual octamers wrt a specific sequence
- active promoters: reduced occupancy
- flanked by two well positioned nucleosomes.
- moved by ATP dependent complexes such as SWI/SNF, ISWI, INO80, SWR, Mi-2/CHD
Chromosome looping
can bring together long range regulatory elements
- in cis (on the same chromosome, TH2 LCR)
- in trans (between chromosomes) chr10 IFNg and chr11(IL4)
Cis regulatory elements
the DNA elements that control gene epression and constitute an integral part of the gene struction. Contain the binding sites for trans-activating factors serve as the sites of epigenetic modification