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Hsf1 的调控和热休克反应。

Regulation of Hsf1 and the Heat Shock Response.

机构信息

Department of Molecular Genetics and Cell Biology, Center for Physics of Evolving Systems, University of Chicago, Chicago, IL, USA.

出版信息

Adv Exp Med Biol. 2020;1243:41-50. doi: 10.1007/978-3-030-40204-4_3.

Abstract

The heat shock response (HSR) is characterized by the induction of molecular chaperones following a sudden increase in temperature. In eukaryotes, the HSR comprises the set of genes controlled by the transcription factor Hsf1. The HSR is induced by defects in co-translational protein folding, ribosome biogenesis, organellar targeting of nascent proteins, and protein degradation by the ubiquitin proteasome system. Upon heat shock, these processes may be endogenous sources of polypeptide ligands that activate the HSR. Mechanistically, these ligands are thought to titrate the chaperone Hsp70 away from Hsf1, releasing Hsf1 to induce the full arsenal of cellular chaperones to restore protein homeostasis. In metazoans, this cell-autonomous feedback loop is modulated by the microenvironment and neuronal cues to enable tissue-level and organism-wide coordination.

摘要

热激反应(HSR)的特征是在温度突然升高后诱导分子伴侣。在真核生物中,HSR 由转录因子 Hsf1 控制的一组基因组成。HSR 是由共翻译蛋白折叠、核糖体生物发生、新生蛋白的细胞器靶向以及泛素蛋白酶体系统的蛋白降解缺陷引起的。在热激后,这些过程可能是激活 HSR 的多肽配体的内源性来源。从机制上讲,这些配体被认为可以使伴侣蛋白 Hsp70 从 Hsf1 上滴定下来,从而释放 Hsf1 来诱导全套细胞伴侣以恢复蛋白质的内稳态。在后生动物中,这种细胞自主的反馈环被微环境和神经元信号所调节,以实现组织水平和全器官的协调。

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