Grass carp (Ctenopharyngodon idella) deacetylase SIRT1 targets p53 to suppress apoptosis in a KAT8 dependent or independent manner

被引:5
作者
Li, Meifeng [1 ,2 ,3 ]
Hu, Jihuan [3 ]
Zhou, Jiazhan [3 ]
Wu, Chuxin [4 ]
Li, Dongming [5 ]
Mao, Huiling [3 ]
Kong, Lingbao [1 ,2 ]
Hu, Chengyu [3 ,6 ]
Xu, Xiaowen [3 ,6 ]
机构
[1] Jiangxi Agr Univ, Inst Pathogen Microorganism, Nanchang 330045, Peoples R China
[2] Jiangxi Agr Univ, Coll Biosci & Engn, Nanchang 330045, Peoples R China
[3] Nanchang Univ, Sch Life Sci, Nanchang 330031, Peoples R China
[4] Yuzhang Normal Univ, Dept Nat Sci, Nanchang 330103, Peoples R China
[5] Nanchang Univ, Fuzhou Med Coll, Fuzhou 344000, Peoples R China
[6] Nanchang Univ, Sch Life Sci, Dept Biosci, Nanchang 330031, Peoples R China
基金
中国国家自然科学基金;
关键词
Acetylation; Apoptosis; Fish; SIRT1; KAT8; p53; ACETYLTRANSFERASE; ACETYLATION;
D O I
10.1016/j.fsi.2023.109264
中图分类号
S9 [水产、渔业];
学科分类号
0908 ;
摘要
Sirtuin1 (SIRT1) is known as a deacetylase to control various physiological processes. In mammals, SIRT1 inhibits apoptotic process, but the detailed mechanism is not very clear. Here, our study revealed that grass carp (Ctenopharyngodon idella) SIRT1 (CiSIRT1, MN125614.1) inhibits apoptosis through targeting p53 in a KAT8dependent or a KAT8-independent manner. In CIK cells, CiSIRT1 over-expression results in significant decrease of some apoptotic gene expressions, including Bax/Bcl2, caspase3 and caspase9, whereas CiKAT8 or Cip53 facilitates the induction of apoptosis. Because CiSIRT1 separately interacted with CiKAT8 and Cip53, we speculated that CiSIRT1 blocked apoptosis may be by virtue of KAT8-p53 axis or directly by p53. In a KAT8dependent manner, CiSIRT1 interacted with CiKAT8, then reduced the acetylation of CiKAT8 and subsequently promoted its degradation. Then, CiKAT8 acetylated p53 and induced p53-mediated apoptosis. MYST domain of CiKAT8 was critical in this pathway. In a KAT8-independent manner, CiSIRT1 also inhibited p53induced apoptosis by directly deacetylating p53 and promoting the degradation of p53. Generally, these findings uncovered two pathways in which CiSIRT1 decreases the acetylation of p53 via a KAT8-dependent or a KAT8-independent manner.
引用
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页数:13
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