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在酵母中删除转录因子 Hsf1、Msn2 和 Msn4 揭示了应对蛋白毒性应激的转录重编程。

Deletion of the transcription factors Hsf1, Msn2 and Msn4 in yeast uncovers transcriptional reprogramming in response to proteotoxic stress.

机构信息

Center for Protein Assemblies, Department of Bioscience, Technische Universität München, Garching, Germany.

Institute of Bioinformatics, Department of Informatics, Ludwig-Maximilians-Universität München, München, Germany.

出版信息

FEBS Lett. 2024 Mar;598(6):635-657. doi: 10.1002/1873-3468.14821. Epub 2024 Feb 16.

Abstract

The response to proteotoxic stresses such as heat shock allows organisms to maintain protein homeostasis under changing environmental conditions. We asked what happens if an organism can no longer react to cytosolic proteotoxic stress. To test this, we deleted or depleted, either individually or in combination, the stress-responsive transcription factors Msn2, Msn4, and Hsf1 in Saccharomyces cerevisiae. Our study reveals a combination of survival strategies, which together protect essential proteins. Msn2 and 4 broadly reprogram transcription, triggering the response to oxidative stress, as well as biosynthesis of the protective sugar trehalose and glycolytic enzymes, while Hsf1 mainly induces the synthesis of molecular chaperones and reverses the transcriptional response upon prolonged mild heat stress (adaptation).

摘要

在应对热休克等蛋白毒性应激时,生物体能够在不断变化的环境条件下维持蛋白质的内稳态。我们想知道,如果生物体不能再对细胞质蛋白毒性应激做出反应,会发生什么。为了测试这一点,我们在酿酒酵母中单独或组合缺失或耗尽了应激反应转录因子 Msn2、Msn4 和 Hsf1。我们的研究揭示了一系列生存策略的组合,这些策略共同保护了必需蛋白。Msn2 和 4 广泛地重新编程转录,引发对氧化应激的反应,以及保护性糖海藻糖和糖酵解酶的生物合成,而 Hsf1 主要诱导分子伴侣的合成,并在长时间轻度热应激(适应)时逆转转录反应。

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