Metabolic Regulation of Epigenetics
Open accessAbstract
How cells sense and respond to environmental cues remains a central question of biological research. Recent evidence suggests that DNA transcription is regulated by chromatin organization. However, the mechanism for relaying the cytoplasmic signaling to chromatin remodeling remains incompletely understood. Although much emphasis has been put on delineating transcriptional output of growth factor/hormonal signaling pathways, accumulated evidence from yeast and mammalian systems suggest that metabolic signals also play critical roles in determining chromatin structure. Here we summarize recent progress in understanding the molecular connection between metabolism and epigenetic modifications of chromatin implicated in a variety of diseases including cancer.
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Glucose is a key molecule in transcriptional processes.
“Glucose is a key molecule in transcriptional processes.”
From 2-Deoxyglucose drives plasticity via an adaptive ER stress-ATF4 pathway and elicits stroke recovery and Alzheimer’s resilience (2023) · cites this paper as [47]
The Introduction says metabolism plays a significant role in transcription, and the section on yeast metabolic cycles links products of glucose metabolism, especially acetyl-CoA, to histone acetylation and gene transcription. This supports a connection between glucose metabolism and transcription, but does not establish that glucose itself is a key molecule in transcriptional processes. (LLM, conf=0.82)
Experimental — accuracy not yet measuredMetabolic intermediates of the TCA cycle affect epigenetic control of gene expression by regulating histone and DNA modifications.
“metabolic intermediates of the TCA cycle affect epigenetic-mediated control of gene expression through regulating the modification of histones and DNA 137,138”
From Inside and out: the activities of senescence in cancer (2014) · cites this paper as [138]
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References 95 · Cited by 699
- Authors
- Lu, C., & Thompson, C. B.
- Affiliations
- Memorial Sloan Kettering Cancer Center (US)
- Corresponding author
- Thompson, Craig B.
- ORCID
- Thompson, Craig B.
- Venue
- Cell Metabolism
- Publisher
- Elsevier BV
- Published
- 2012-07
- Volume
- 16
- Issue
- 1
- Pages
- 9-17
- ISSN
- 1550-4131 (ISSN-L)
- PMC
- PMC3392647
- OpenAlex
- W2147494386
- Cited by
- 699
- References
- 95
- Citations by year
- 2026: 52 · 2025: 42 · 2024: 33 · 2023: 47 · 2022: 68 · 2021: 46 · 2020: 62 · 2019: 53 · 2018: 54 · 2017: 46 · 2016: 54 · 2015: 57 · 2014: 51 · 2013: 27 · 2012: 4
- FWCI
- 17.88
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- Locations
- Cell Metabolism (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Agios Pharmaceuticals
- National Institutes of Health
- National Cancer Institute (P01CA104838, R01CA105463)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Epigenetics and DNA Methylation
- 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
- chromatin remodeling, chromatin organization, DNA transcription, cytoplasmic signaling, epigenetic modifications, cancer, growth factor signaling, hormone signaling, yeast, mammalian cells
- MeSH terms
- Animals, Circadian Rhythm, Histones, Humans, Neoplasms, Protein Processing, Post-Translational, Saccharomyces cerevisiae, DNA Methylation, Feedback, Physiological, Chromatin Assembly and Disassembly, Epigenesis, Genetic
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