Control of gene expression and the cell cycle
Abstract
The pRb tumour suppressor protein is an essential component of the cell-cycle clock, integrating both positive and negative signals for cellular growth and proliferation with the transcription machinery. pRb exerts its tumour suppression function by both antagonizing and synergizing with downstream effectors, such as E2F. pRb has two modes of action, it can inactivate E2F transcription activity or it can assemble an active repression complex with E2F. Apart from E2F, pRb interacts with various factors to promote cellular differentiation. The differentiation properties of pRb are likely to contribute partly to its tumour suppressor function. It is also clear that pRb is a master regulator for transcription. It can both activate and repress transcription in a context-dependent manner. pRb interacts directly with histone acetyltransferase, histone deacetylases and SWI/SNF proteins, all of which are classes of proteins involved in chromatin remodelling. Last, but not least, pRb regulates transcription driven by all three polymerases, thereby integrating the cell-cycle clock with the biosynthetic capacity of the cell in controlling cellular proliferation and growth.
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SWI/SNF recruits the chromatin activators P300 and CBP, which mediate acetylation of histone H3 lysine 27 through their intrinsic histone acetyltransferase activity.
“SWI/SNF recruits the chromatin activators P300 and CBP, which mediate the acetylation of histone H3 lysine 27 through their intrinsic histone acetyltransferase (HAT) activity [59–62].”
From Transcriptional enhancers and their communication with gene promoters (2021) · cites this paper as [59]
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Transcriptional enhancers and their communication with gene promoters
Ray-Jones, H., & Spivakov, M. (2021) · Cellular and Molecular Life Sciences · doi:10.1007/s00018-021-03903-w · Cited by 81 · see citing works
- Authors
- Chan, H. M., Shikama, N., & La Thangue, N. B.
- Affiliations
- University of Glasgow (GB)
- Division of Biochemistry and Molecular Biology, Davidson Building, University of Glasgow, Glasgow G12 8QQ, U.K.
- ORCID
- Chan, Ho Man
- Venue
- Essays in Biochemistry
- Publisher
- Portland Press Ltd.
- Published
- 2001-05-01
- Volume
- 37
- Pages
- 87-96
- ISSN
- 0071-1365 (ISSN-L)
- 1744-1358
- OpenAlex
- W297574228
- Cited by
- 11
- References
- 0
- Citations by year
- 2021: 1 · 2013: 1 · 2012: 1
- FWCI
- 1.03
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Essays in Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Oncology › Cancer-related Molecular Pathways
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Keywords
- retinoblastoma protein, tumor suppressor proteins, cell cycle regulation, E2F transcription factors, transcriptional repression, chromatin remodeling, histone acetyltransferase, histone deacetylase, SWI/SNF complex, cell differentiation, transcriptional activation, RNA polymerase, cell proliferation
- MeSH terms
- Animals, Cell Cycle, Cell Line, DNA-Binding Proteins, Gene Expression Regulation, Humans, Models, Genetic, Phosphorylation, Transcription Factors, Retinoblastoma Protein, Protein Structure, Tertiary, Cell Cycle Proteins, E2F Transcription Factors
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