A maternal high-fat diet modulates fetal SIRT1 histone and protein deacetylase activity in nonhuman primates

Melissa A. Suter, Aishe Chen, Marie S. Burdine, Mahua Choudhury, R. Alan Harris, Robert H. Lane, Jacob E. Friedman, Kevin L. Grove, Alan J. Tackett, Kjersti M. Aagaard

    Research output: Contribution to journalArticlepeer-review

    140 Scopus citations


    In nonhuman primates, we previously demonstrated that a maternal high-fat diet (MHFD) induces fetal nonalcoholic fatty liver disease (NAFLD) and alters the fetal metabolome. These changes are accompanied by altered acetylation of histone H3 (H3K14ac). However, the mechanism behind this alteration in acetylation remains unknown. As SIRT1 is both a lysine deacetylase and a crucial sensor of cellular metabolism, we hypothesized that SIRT1 may be involved in fetal epigenomic alterations. Here we show that in utero exposure to a MHFD, but not maternal obesity per se, increases fetal H3K14ac with concomitant decreased SIRT1 expression and diminished in vitro protein and histone deacetylase activity. MHFD increased H3K14ac and DBC1-SIRT1 complex formation in fetal livers, both of which were abrogated with diet reversal despite persistent maternal obesity. Moreover, MHFD was associated with altered expression of known downstream effectors deregulated in NAFLD and modulated by SIRT1 (e.g., PPARA, PPARG, SREBF1, CYP7A1, FASN, and SCD). Finally, ex vivo purified SIRT1 retains deacetylase activity on an H3K14ac peptide substrate with preferential activity toward acetylated histone H3; mutagenesis of the catalytic domain of SIRT1 (H363Y) abrogates H3K14ac deacetylation. Our data implicate SIRT1 as a likely molecular mediator of the fetal epigenome and metabolome under MHFD conditions.

    Original languageEnglish (US)
    Pages (from-to)5106-5114
    Number of pages9
    JournalFASEB Journal
    Issue number12
    StatePublished - Dec 2012


    • Developmental origins of adult disease
    • Epigenetics
    • Histone modification
    • NAFLD
    • Sirtuins

    ASJC Scopus subject areas

    • Biotechnology
    • Biochemistry
    • Molecular Biology
    • Genetics


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