Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
2047433 | FEBS Letters | 2015 | 8 Pages |
Abstract
By using acetyl-CoA as a substrate, acetyltransferases and histone deacetylases regulate protein acetylation by adding or removing an acetyl group on lysines. Nuclear-located Hdac1 is a regulator of intestinal homeostasis. We have previously shown that Hdac1 define specific intestinal epithelial cell basal and inflammatory-dependent gene expression patterns and control cell proliferation. We show here that Hdac1 depletion in cellulo leads to increased histone acetylation after metabolic stresses, and to metabolic disturbances resulting in impaired responses to oxidative stresses, AMPK kinase activation and mitochondrial biogenesis. Thus, nuclear Hdac1 may control intestinal epithelial cell metabolism by regulating the supply of acetyl groups.
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Authors
Alexis Gonneaud, Naomie Turgeon, François-Michel Boisvert, François Boudreau, Claude Asselin,