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Short-chain fatty acids propionate and butyrate control growth and differentiation linked to cellular metabolism.
Nshanian, Michael; Geller, Benjamin S; Gruber, Joshua J; Chleilat, Faye; Camarillo, Jeannie Marie; Kelleher, Neil L; Zhao, Yingming; Snyder, Michael P.
Afiliação
  • Nshanian M; Department of Genetics, Stanford University, School of Medicine, Stanford, CA.
  • Geller BS; Department of Genetics, Stanford University, School of Medicine, Stanford, CA.
  • Gruber JJ; Department of Genetics, Stanford University, School of Medicine, Stanford, CA.
  • Chleilat F; Department of Genetics, Stanford University, School of Medicine, Stanford, CA.
  • Camarillo JM; Department of Chemistry, Molecular Biosciences and Proteomics Center of Excellence, Northwestern University, Evanston, IL.
  • Kelleher NL; Department of Chemistry, Molecular Biosciences and Proteomics Center of Excellence, Northwestern University, Evanston, IL.
  • Zhao Y; Department of Biochemistry and Molecular Genetics, Feinberg School of Medicine, Northwestern University, Evanston, IL.
  • Snyder MP; Ben May Department of Cancer Research Committee on Cancer Biology, University of Chicago; Chicago, IL.
Res Sq ; 2024 Feb 16.
Article em En | MEDLINE | ID: mdl-38410440
ABSTRACT
The short-chain fatty acids (SCFA) propionate and butyrate are produced in large amounts by microbial metabolism and have been identified as unique acyl lysine histone marks. In order to better understand the function of these modifications we used ChIP-seq to map the genome-wide location of four short-chain acyl histone marks H3K18pr/bu and H4K12pr/bu 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 along with gene expression to access the function of the target regions. Our data demonstrate that propionate and butyrate act as promoters of growth, differentiation as well as ion transport. We propose a mechanism involving direct modification of specific genomic regions, resulting in increased chromatin accessibility, and in case of butyrate, opposing effects on the proliferation of normal versus CRC cells.

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Res Sq Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Res Sq Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá