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PRC1 drives Polycomb-mediated gene repression by controlling transcription initiation and burst frequency

Abstract:
The Polycomb repressive system plays a fundamental role in controlling gene expression during mammalian development. To achieve this, Polycomb repressive complexes 1 and 2 (PRC1 and PRC2) bind target genes and use histone modification-dependent feedback mechanisms to form Polycomb chromatin domains and repress transcription. The inter-relatedness of PRC1 and PRC2 activity at these sites has made it difficult to discover the specific components of Polycomb chromatin domains that drive gene repression and to understand mechanistically how this is achieved. Here, by exploiting rapid degron-based approaches and time-resolved genomics, we kinetically dissect Polycomb-mediated repression and discover that PRC1 functions independently of PRC2 to counteract RNA polymerase II binding and transcription initiation. Using single-cell gene expression analysis, we reveal that PRC1 acts uniformly within the cell population and that repression is achieved by controlling transcriptional burst frequency. These important new discoveries provide a mechanistic and conceptual framework for Polycomb-dependent transcriptional control.
Publication status:
Published
Peer review status:
Peer reviewed

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Publisher copy:
10.1038/s41594-021-00661-y

Authors

More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Biochemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Biochemistry
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MSD
Department:
Biochemistry
Oxford college:
Exeter College
Role:
Author
ORCID:
0000-0002-8726-7888


More from this funder
Funder identifier:
https://ror.org/029chgv08
Grant:
209400/Z/17/Z
More from this funder
Funder identifier:
https://ror.org/0472cxd90
Grant:
681440


Publisher:
Springer Nature
Journal:
Nature Structural and Molecular Biology More from this journal
Volume:
28
Issue:
10
Pages:
811-824
Publication date:
2021-10-04
Acceptance date:
2021-08-10
DOI:
EISSN:
1545-9985
ISSN:
1545-9993
Pmid:
34608337


Language:
English
Keywords:
Pubs id:
1200133
Local pid:
pubs:1200133
Source identifiers:
W3204751963
Deposit date:
2026-03-09
ARK identifier:

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