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Roles of His_(101) in DNA-Binding Domain of Human Heat Shock Factor 1 Under Acid pH Environment

机译:酸性pH环境下His_(101)在人类热激因子1 DNA结合域中的作用

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摘要

The cellular response to acute and proteotoxic stresses, historically called "heat shock response" (HSR), is strongly conserved throughout all known organisms. Heat shock factor 1 (HSF1) was first characterized as a major transcription factor during HSR, by its potentialities to regulate the expression of heat shock proteins (HSPs, also known as molecular chaperones). In most tissues and cell types, HSF1 is constitutively expressed, and is kept inactive in the absence of stress. Under the abnormal conditions, HSF1 homo-trimer is formed by three monomeric ones, and exhibits its DNA-binding and post-translational activities (inducing the expression of downstream HSP genes). Recent studies have reported that HSF1 plays a powerful multi-faceted role in tumor growth and response to cancer therapy.
机译:历史上称为“热休克反应”(HSR)的细胞对急性和蛋白毒性应激的反应在所有已知生物中都得到了高度保守。热休克因子1(HSF1)首先被表征为HSR中的主要转录因子,因为它具有调节热休克蛋白(HSPs,也称为分子伴侣)表达的潜力。在大多数组织和细胞类型中,HSF1组成型表达,在没有压力的情况下保持无活性。在异常情况下,HSF1同型三聚体由三个单体形成,并表现出其DNA结合和翻译后活性(诱导下游HSP基因的表达)。最近的研究报道,HSF1在肿瘤生长和对癌症治疗的反应中起着强大的多方面作用。

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