Regulation of TFEB nuclear localization by HSP90AA1 promotes autophagy and longevity

TFEB 自噬 生物 细胞生物学 雷帕霉素的作用靶点 碱性螺旋-环-螺旋-亮氨酸拉链转录因子 尼泊尔卢比1 袋3 转录因子 遗传学 基因 DNA结合蛋白 细胞凋亡
作者
Shaosong Yang,Tiejian Nie,Hua She,Kai Tao,Fangfang Lu,Yiman Hu,Lu Huang,Lin Zhu,Dayun Feng,Dalin He,Ji Qi,Thomas Kukar,Long Ma,Zixu Mao,Qian Yang
出处
期刊:Autophagy [Informa]
卷期号:19 (3): 822-838 被引量:7
标识
DOI:10.1080/15548627.2022.2105561
摘要

ABSTRACTTFEB (transcription factor EB) regulates multiple genes involved in the process of macroautophagy/autophagy and plays a critical role in lifespan determination. However, the detailed mechanisms that regulate TFEB activity are not fully clear. In this study, we identified a role for HSP90AA1 in modulating TFEB. HSP90AA1 was phosphorylated by CDK5 at Ser 595 under basal condition. This phosphorylation inhibited HSP90AA1, disrupted its binding to TFEB, and impeded TFEB’s nuclear localization and subsequent autophagy induction. Pro-autophagy signaling attenuated CDK5 activity and enhanced TFEB function in an HSP90AA1-dependent manner. Inhibition of HSP90AA1 function or decrease in its expression significantly attenuated TFEB’s nuclear localization and transcriptional function following autophagy induction. HSP90AA1-mediated regulation of a TFEB ortholog was involved in the extended lifespan of Caenorhabditis elegans in the absence of its food source bacteria. Collectively, these findings reveal that this regulatory process plays an important role in modulation of TFEB, autophagy, and longevity.Abbreviations : AL: autolysosome; AP: autophagosome; ATG: autophagy related; BafA1: bafilomycin A1; CDK5: cyclin-dependent kinase 5; CDK5R1: cyclin dependent kinase 5 regulatory subunit 1; CR: calorie restriction; FUDR: 5-fluorodeoxyuridine; HSP90AA1: heat shock protein 90 alpha family class A member 1; MAP1LC3: microtubule associated protein 1 light chain 3; NB: novobiocin sodium; SQSTM1: sequestosome 1; TFEB: transcription factor EB; WT: wild type.KEYWORDS: AgingCDK5macroautophagyphosphorylationtranscriptional factor AcknowledgmentsWe thank Hong Zhang for the C. elegans strain of MAH235.Disclosure statementThe authors declare that they have no competing interests.Supplementary materialSupplemental data for this article can be accessed online at https://doi.org/10.1080/15548627.2022.2105561Additional informationFundingThis work was supported by the National Natural Science Foundation of China [81720108016]; National Natural Science Foundation of China [31930048]; National Natural Science Foundation of China [31671060].
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