Sirt6 deacetylase activity regulates circadian rhythms via Per2

被引:15
|
作者
Sun, Shimin [1 ,2 ]
Liu, Zuojun [3 ,4 ,5 ]
Feng, Yukun [6 ]
Shi, Lei [6 ]
Cao, Xinyue [3 ,4 ,5 ]
Cai, Yanlin [3 ,4 ,5 ]
Liu, Baohua [3 ,4 ,5 ]
机构
[1] Shandong Univ Technol, Antiaging & Regenerat Med Res Inst, Sch Life Sci, Zibo 255049, Shandong, Peoples R China
[2] Shandong Univ Technol, Lab Dev & Evolutionary Biol, Sch Life Sci, Zibo 255049, Shandong, Peoples R China
[3] Shenzhen Univ, Hlth Sci Ctr, Guangdong Key Lab Genome Stabil & Human Dis Preve, Shenzhen 518055, Peoples R China
[4] Shenzhen Univ, Hlth Sci Ctr, Med Res Ctr, Shenzhen 518055, Peoples R China
[5] Shenzhen Univ, Hlth Sci Ctr, Dept Biochem & Mol Biol, Shenzhen 518055, Peoples R China
[6] Univ Hong Kong, Sch Biomed Sci, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
Sirt6; Deacetylation; Degradation; Per2; Circadian clock; DNA-DAMAGE; GENOMIC INSTABILITY; TUMOR SUPPRESSION; GENE-EXPRESSION; LIFE-SPAN; CLOCK; METABOLISM; SLEEP; PHOSPHORYLATION; ACETYLATION;
D O I
10.1016/j.bbrc.2019.01.143
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Circadian clock relies on a transcription and translation feedback loop (TTFL). Two transcription factors, i.e. Bmal1 and Clock, activate the transcription of Period (Per) and Cryptochrome (Cry), which inhibit their own transcription when accumulated to a critical concentration. NAD(+)-dependent deacylase Sirt1 deacetylates Bmal1 and Per2 to regulate circadian rhythms. Sirt6 interacts with Bmal1 to regulate clock-controlled gene (CCG) expression by local chromatin remodeling. Whether Sirt6 directly modify clock components is elusive. Here, we found that loss of Sirt6 jeopardizes circadian phase. At molecular level, Sirt6 interacts with and deacetylates Per2, thus preventing its proteasomal degradation. These data highlight an important function of Sirt6 in the direct regulation of TTFL and circadian rhythms. (C) 2019 Published by Elsevier Inc.
引用
收藏
页码:234 / 238
页数:5
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