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The molecular principles of gene regulation by Polycomb repressive complexes
- Source :
- Nature reviews. Molecular cell biology
- Publication Year :
- 2021
- Publisher :
- Springer Science and Business Media LLC, 2021.
-
Abstract
- Precise control of gene expression is fundamental to cell function and development. Although ultimately gene expression relies on DNA-binding transcription factors to guide the activity of the transcription machinery to genes, it has also become clear that chromatin and histone post-translational modification have fundamental roles in gene regulation. Polycomb repressive complexes represent a paradigm of chromatin-based gene regulation in animals. The Polycomb repressive system comprises two central protein complexes, Polycomb repressive complex 1 (PRC1) and PRC2, which are essential for normal gene regulation and development. Our early understanding of Polycomb function relied on studies in simple model organisms, but more recently it has become apparent that this system has expanded and diverged in mammals. Detailed studies are now uncovering the molecular mechanisms that enable mammalian PRC1 and PRC2 to identify their target sites in the genome, communicate through feedback mechanisms to create Polycomb chromatin domains, and control transcription to regulate gene expression. In this Review, we discuss and contextualise the emerging principles that define how this fascinating chromatin-based system regulates gene expression in mammals.
- Subjects :
- Polycomb Repressive Complex 1
Regulation of gene expression
Transcription, Genetic
biology
Polycomb Repressive Complex 2
Ubiquitination
macromolecular substances
Cell Biology
Methylation
Chromatin
Article
Cell biology
Histones
Histone
Gene Expression Regulation
Gene expression
biology.protein
Humans
PRC1
PRC2
Protein Processing, Post-Translational
Molecular Biology
Gene
Transcription factor
Subjects
Details
- ISSN :
- 14710080 and 14710072
- Volume :
- 22
- Database :
- OpenAIRE
- Journal :
- Nature Reviews Molecular Cell Biology
- Accession number :
- edsair.doi.dedup.....c1dca36e396cb28492c41492dffb8018
- Full Text :
- https://doi.org/10.1038/s41580-021-00398-y