Biological control through regulated transcriptional coactivators
Open accessAbstract
Gene activation in higher eukaryotes requires the concerted action of transcription factors and coactivator proteins. Coactivators exist in multiprotein complexes that dock on transcription factors and modify chromatin, allowing effective transcription to take place. While biological control focused at the level of the transcription factor is very common, it is now quite clear that a substantial component of gene control is directed at the expression of coactivators, involving pathways as diverse as B-cell development, smooth muscle differentiation, and hepatic gluconeogenesis. Quantitative control of coactivators allows the functional integration of multiple transcription factors and facilitates the formation of distinct biological programs. This coordination and acceleration of different steps in linked pathways has important kinetic considerations, enabling outputs of particular pathways to be increased far more than would otherwise be possible. These kinetic aspects suggest opportunities and concerns as coactivators become targets of therapeutic intervention.
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Increased PCG1α is consistent with increased mitochondrial biogenesis.
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From Comprehensive Multi-omics Analysis Reveals Mitochondrial Stress as a Central Biological Hub for Spaceflight Impact (2020) · cites this paper as Spiegelman and Heinrich, 2004
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- Authors
- Spiegelman, B. M., & Heinrich, R.
- Affiliations
- Harvard University (US)
- Humboldt-Universität zu Berlin (DE)
- Corresponding author
- Spiegelman, Bruce M.
- ORCID
- Spiegelman, Bruce M.
- Venue
- Cell
- Publisher
- Elsevier BV
- Published
- 2004-10
- Volume
- 119
- Issue
- 2
- Pages
- 157-167
- ISSN
- 0092-8674 (ISSN-L)
- OpenAlex
- W2050175422
- Cited by
- 377
- References
- 92
- Citations by year
- 2026: 6 · 2025: 7 · 2024: 13 · 2023: 14 · 2022: 9 · 2021: 9 · 2020: 11 · 2019: 9 · 2018: 11 · 2017: 4 · 2016: 9 · 2015: 14 · 2014: 11 · 2013: 20 · 2012: 16
- FWCI
- 2.61
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.elsevier.com/tdm/userlicense/1.0/ (tdm)
- www.elsevier.com/legal/tdmrep-license (tdm)
- www.elsevier.com/open-access/userlicense/1.0/ (vor, 3211 d)
- doi.org/10.15223/policy-017 (stm-asf)
- doi.org/10.15223/policy-037 (stm-asf)
- doi.org/10.15223/policy-012 (stm-asf)
- doi.org/10.15223/policy-029 (stm-asf)
- doi.org/10.15223/policy-004 (stm-asf)
- Locations
- Cell (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute of Diabetes and Digestive and Kidney Diseases (DK54477, R01DK061562, DK 61562)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Genomics and Chromatin Dynamics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Gene Regulatory Network Analysis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Chromatin Remodeling and Cancer
- Keywords
- transcriptional coactivator, gene expression regulation, chromatin modification, transcription factors, B cell development, smooth muscle differentiation, hepatic gluconeogenesis, kinetic control, therapeutic target
- MeSH terms
- Animals, B-Lymphocytes, Gene Expression Regulation, Models, Genetic, Nuclear Proteins, Transcription Factors, Transcription, Genetic, Transcriptional Activation, Trans-Activators, Chromatin Assembly and Disassembly, Macromolecular Substances
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