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KDM2 proteins constrain transcription from CpG island gene promoters independently of their histone demethylase activity
- Source :
- Nucleic Acids Research
-
Abstract
- CpG islands (CGIs) are associated with the majority of mammalian gene promoters and function to recruit chromatin modifying enzymes. It has therefore been proposed that CGIs regulate gene expression through chromatin-based mechanisms, however in most cases this has not been directly tested. Here, we reveal that the histone H3 lysine 36 (H3K36) demethylase activity of the CGI-binding KDM2 proteins contributes only modestly to the H3K36me2-depleted state at CGI-associated gene promoters and is dispensable for normal gene expression. Instead, we discover that KDM2 proteins play a widespread and demethylase-independent role in constraining gene expression from CGI-associated gene promoters. We further show that KDM2 proteins shape RNA Polymerase II occupancy but not chromatin accessibility at CGI-associated promoters. Together this reveals a demethylase-independent role for KDM2 proteins in transcriptional repression and uncovers a new function for CGIs in constraining gene expression.
- Subjects :
- Jumonji Domain-Containing Histone Demethylases
Transcription, Genetic
RNA polymerase II
Histones
03 medical and health sciences
Histone H3
Mice
0302 clinical medicine
Demethylase activity
Gene expression
mental disorders
Genetics
Animals
Humans
Histone demethylase activity
Promoter Regions, Genetic
030304 developmental biology
Regulation of gene expression
0303 health sciences
biology
Models, Genetic
F-Box Proteins
Lysine
Gene regulation, Chromatin and Epigenetics
Promoter
Mouse Embryonic Stem Cells
DNA Methylation
Chromatin
3. Good health
Cell biology
HEK293 Cells
CpG site
Gene Expression Regulation
030220 oncology & carcinogenesis
biology.protein
CpG Islands
RNA Polymerase II
030217 neurology & neurosurgery
Subjects
Details
- Language :
- English
- ISSN :
- 13624962 and 03051048
- Volume :
- 47
- Issue :
- 17
- Database :
- OpenAIRE
- Journal :
- Nucleic Acids Research
- Accession number :
- edsair.doi.dedup.....64e6ddcc5fd5545c8f439336269a9122
- Full Text :
- https://doi.org/10.1093/nar/gkz607