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热休克因子编码:指定多种广泛促进应激恢复力的转录调控程序。

The heat shock factor code: Specifying a diversity of transcriptional regulatory programs broadly promoting stress resilience.

作者信息

Alasady Milad J, Mendillo Marc L

机构信息

Department of Biochemistry and Molecular Genetics, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA; Simpson Querrey Center for Epigenetics, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA; Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.

Department of Biochemistry and Molecular Genetics, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA; Simpson Querrey Center for Epigenetics, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA; Robert H. Lurie Comprehensive Cancer Center, Northwestern University Feinberg School of Medicine, Chicago, IL 60611, USA.

出版信息

Cell Stress Chaperones. 2024 Dec;29(6):735-749. doi: 10.1016/j.cstres.2024.10.006. Epub 2024 Oct 23.

Abstract

The heat shock factor (HSF) family of transcription factors drives gene expression programs that maintain cytosolic protein homeostasis (proteostasis) in response to a vast array of physiological and exogenous stressors. The importance of HSF function has been demonstrated in numerous physiological and pathological contexts. Evidence accumulating over the last two decades has revealed that the regulatory programs driven by the HSF family can vary dramatically depending on the context in which it is activated. To broadly maintain proteostasis across these contexts, HSFs must bind and appropriately regulate the correct target genes at the correct time. Here, we discuss "the heat shock factor code"-our current understanding of how human cells use HSF paralog diversification and interplay, local concentration, post-translational modifications, and interactions with other proteins to enable the functional plasticity required for cellular resilience across a multitude of environments.

摘要

热休克因子(HSF)转录因子家族驱动基因表达程序,以响应大量生理和外源性应激源来维持胞质蛋白质稳态(蛋白质平衡)。HSF功能的重要性已在众多生理和病理环境中得到证实。过去二十年积累的证据表明,HSF家族驱动的调控程序会因激活环境的不同而有很大差异。为了在这些环境中广泛维持蛋白质平衡,HSF必须在正确的时间结合并适当地调控正确的靶基因。在这里,我们讨论“热休克因子密码”——我们目前对人类细胞如何利用HSF旁系同源物的多样化和相互作用、局部浓度、翻译后修饰以及与其他蛋白质的相互作用,以实现细胞在多种环境中恢复力所需的功能可塑性的理解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8f5c/11570959/455c81d215ef/gr1.jpg

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