KAT8 acetylation-controlled lipolysis affects the invasive and migratory potential of colorectal cancer cells
Qiu Bingquan, Li Shen, Li Meiting, Wang Shuo, Mu Guanqun, Chen Keyu, Wang Meng, Zhu Wei-guo, Wang Weibin, Wang Jiadong, Li Ziyu, Yang Jichun, Yang Yang
Journal:Cell Death & Disease
IF:9
DOI:10.1038/s41419-023-05582-w
PMID:36849520
Published:2023-02-27
research field:分子生物学癌症生物学基因组学RNA生物学转录组学
Abstract
Epigenetic mechanisms involved in gene expression play an essential role in various cellular processes, including lipid metabolism. Lysine acetyltransferase 8 (KAT8), a histone acetyltransferase, has been reported to mediate de novo lipogenesis by acetylating fatty acid synthase. However, the effect of KAT8 on lipolysis is unclear. Here, we report a novel mechanism of KAT8 on lipolysis involving in its acetylation by general control non-repressed protein 5 (GCN5) and its deacetylation by Sirtuin 6 (SIRT6). KAT8 acetylation at K168/175 residues attenuates the binding activity of KAT8 and inhibits the recruitment of RNA pol II to the promoter region of the lipolysis-related genes adipose triglyceride lipase ( ATGL ) and hormone-sensitive lipase ( HSL ), subsequently down-regulating lipolysis to affect the invasive and migratory potential of colorectal cancer cells. Our findings uncover a novel mechanism that KAT8 acetylation-controlled lipolysis affects invasive and migratory potential in colorectal cancer cells.
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