Abstract
Aging is accompanied by physiological impairments, which, in insulin-responsive tissues, including the liver, predispose individuals to metabolic disease. However, the molecular mechanisms underlying these changes remain largely unknown. Here, we analyze genome-wide profiles of RNA and chromatin organization in the liver of young (3 months) and old (21 months) mice. Transcriptional changes suggest that derepression of the nuclear receptors PPARα, PPARγ, and LXRα in aged mouse liver leads to activation of targets regulating lipid synthesis and storage, whereas age-dependent changes in nucleosome occupancy are associated with binding sites for both known regulators (forkhead factors and nuclear receptors) and candidates associated with nuclear lamina (Hdac3 and Srf) implicated to govern metabolic function of aging liver. Winged-helix transcription factor Foxa2 and nuclear receptor corepressor Hdac3 exhibit a reciprocal binding pattern at PPARα targets contributing to gene expression changes that lead to steatosis in aged liver.
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•An in vivo genome-wide nucleosome map in the aging liver is described•Foxa2 binds regions of decreased nucleosome occupancy at PPARα targets in old livers•Hdac3 and Srf are implicated in age-dependent metabolic dysfunction•Reciprocal binding of Foxa2 and Hdac3 at PPARα targets contributes to steatosis
Bochkis et al. use genome-wide profiling in the livers of young and old mice to observe age-dependent changes in PPARα targets as well as nucleosome occupancy linked to Foxa2 and Hdac3 binding sites. A reciprocal binding pattern of Foxa2 and Hdac3 at PPARα targets contributes to gene-expression changes that lead to steatosis in the aging liver.
