Short-chain fatty acid metabolites propionate and butyrate are unique epigenetic regulatory elements linking diet, metabolism and gene expression

The short-chain fatty acids (SCFAs) propionate and butyrate have beneficial health effects, are produced in large amounts by microbial metabolism and have been identified as unique acyl lysine histone marks. To better understand the function of these modifications, we used chromatin immunoprecipitation followed by sequencing to map the genome-wide location of four short-chain acyl histone marks, H3K18pr, H3K18bu, H4K12pr and H4K12bu, in treated and untreated colorectal cancer (CRC) and normal cells as well as in mouse intestines in vivo. We correlate these marks with open chromatin regions and gene expression to access the function of the target regions. Our data demonstrate that propionate and butyrate bind and act as promoters of genes involved in growth, differentiation and ion transport. We propose a mechanism involving direct modification of specific genomic regions by SCFAs resulting in increased chromatin accessibility and, in the case of butyrate, opposing effects on the proliferation of normal versus CRC cells.

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Publication Details

Journal
Nature Metabolism
Published
2025-01-09
DOI
https://doi.org/10.1038/s42255-024-01191-9
Citations
88
Primary Topic
RNA modifications and cancer
Type
article
Field-Weighted Citation Impact
70.93

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article

Short-chain fatty acid metabolites propionate and butyrate are unique epigenetic regulatory elements linking diet, metabolism and gene expression

Faye Chleilat, Yingming Zhao, Michael Snyder, Samuel M. Lancaster et al.
88 citations
Nature Metabolism
RNA modifications and cancer
70.93
article

Short-chain fatty acid metabolites propionate and butyrate are unique epigenetic regulatory elements linking diet, metabolism and gene expression

Faye Chleilat, Yingming Zhao, Michael Snyder, Samuel M. Lancaster, Joshua James Gruber, Benjamin S. Geller, Shannon M. White, Michael Nshanian, Jeannie M. Camarillo, Neil L. Kelleher, Ludmila Alexandrova
article en
88 citations

Abstract

The short-chain fatty acids (SCFAs) propionate and butyrate have beneficial health effects, are produced in large amounts by microbial metabolism and have been identified as unique acyl lysine histone marks. To better understand the function of these modifications, we used chromatin immunoprecipitation followed by sequencing to map the genome-wide location of four short-chain acyl histone marks, H3K18pr, H3K18bu, H4K12pr and H4K12bu, in treated and untreated colorectal cancer (CRC) and normal cells as well as in mouse intestines in vivo. We correlate these marks with open chromatin regions and gene expression to access the function of the target regions. Our data demonstrate that propionate and butyrate bind and act as promoters of genes involved in growth, differentiation and ion transport. We propose a mechanism involving direct modification of specific genomic regions by SCFAs resulting in increased chromatin accessibility and, in the case of butyrate, opposing effects on the proliferation of normal versus CRC cells.

Nature MetabolismVol. 7(1)
Northwestern University (US), University of Chicago (US), Stanford Medicine (US), Stanford University (US)
Cancer Prevention and Research Institute of Texas, Northwestern University, National Institutes of Health, National Human Genome Research Institute, National Cancer Institute, Division of Cancer Epidemiology and Genetics, National Cancer Institute
Good health and well-being
Openalex Percentile: Top 0%
RNA modifications and cancer
70.93
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