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KAT8 acetylation-controlled lipolysis affects the invasive and migratory potential of colorectal cancer cells.


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.

SUBMITTER: Qiu B 

PROVIDER: S-EPMC9970984 | biostudies-literature | 2023 Feb

REPOSITORIES: biostudies-literature

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KAT8 acetylation-controlled lipolysis affects the invasive and migratory potential of colorectal cancer cells.

Qiu Bingquan B   Li Shen S   Li Meiting M   Wang Shuo S   Mu Guanqun G   Chen Keyu K   Wang Meng M   Zhu Wei-Guo WG   Wang Weibin W   Wang Jiadong J   Li Ziyu Z   Yang Jichun J   Yang Yang Y  

Cell death & disease 20230227 2


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  ...[more]

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