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The chromatin factors SET-26 and HCF-1 oppose the histone deacetylase HDA-1 in longevity and gene regulation in C. elegans.
Emerson, Felicity J; Chiu, Caitlin; Lin, Laura Y; Riedel, Christian G; Zhu, Ming; Lee, Siu Sylvia.
Afiliação
  • Emerson FJ; Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America.
  • Chiu C; Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America.
  • Lin LY; Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America.
  • Riedel CG; Department of Biosciences and Nutrition, Karolinska Institutet, Huddinge, Sweden.
  • Zhu M; National Institute of Biological Sciences, Beijing, China.
  • Lee SS; Department of Molecular Biology and Genetics, Cornell University, Ithaca, New York, United States of America.
bioRxiv ; 2023 Mar 23.
Article em En | MEDLINE | ID: mdl-36993207
ABSTRACT
SET-26, HCF-1, and HDA-1 are highly conserved chromatin factors with key roles in development and aging. Here we present mechanistic insights into how these factors regulate gene expression and modulate longevity in C. elegans. We show that SET-26 and HCF-1 cooperate to regulate a common set of genes, and both antagonize the histone deacetylase HDA-1 to limit longevity. We propose a model in which SET-26 recruits HCF-1 to chromatin in somatic cells, where they stabilize each other at the promoters of a subset of genes, particularly mitochondrial function genes, and regulate their expression. HDA-1 opposes SET-26 and HCF-1 on the regulation of a subset of their common target genes and in longevity. Our findings suggest that SET-26, HCF-1, and HDA-1 comprise a mechanism to fine-tune gene expression and longevity and likely have important implications for the mechanistic understanding of how these factors function in diverse organisms, particularly in aging biology.

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2023 Tipo de documento: Article