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多位点磷酸化对转录因子进行精细调控。

Multisite phosphorylation provides sophisticated regulation of transcription factors.

作者信息

Holmberg Carina I, Tran Stefanie E F, Eriksson John E, Sistonen Lea

机构信息

Dept of Biochemistry, Molecular Biology and Cell Biology, Rice Institute for Biomedical Research, Northwestern University, Evanston, IL, USA.

出版信息

Trends Biochem Sci. 2002 Dec;27(12):619-27. doi: 10.1016/s0968-0004(02)02207-7.

Abstract

Reversible phosphorylation is a prevalent mechanism by which the activity of eukaryotic transcription factors is regulated rapidly in response to changes in the cellular environment. Accumulated evidence has expanded the concept of phosphorylation to a process that provides dynamic and precise tuning of the transactivating potential of a factor, rather than being a static on/off switch. In the case of transcription factors such as heat shock factor 1 (HSF1), p53 and nuclear factor of activated T cells (NFAT), multisite phosphorylation enables several effects to operate within a single factor, thereby functioning as a key to signal integration. Studies on these transcription factors illustrate recent progress in solving the dynamic nature of transcriptional regulation by multisite phosphorylation.

摘要

可逆磷酸化是一种普遍存在的机制,通过该机制,真核转录因子的活性可根据细胞环境的变化而迅速调节。越来越多的证据表明,磷酸化已扩展为一个过程,该过程能够动态、精确地调节转录因子的反式激活潜力,而不仅仅是一个静态的开/关开关。就热休克因子1(HSF1)、p53和活化T细胞核因子(NFAT)等转录因子而言,多位点磷酸化可使单一转录因子产生多种效应,从而成为信号整合的关键。对这些转录因子的研究表明,在解决多位点磷酸化介导的转录调控动态性质方面取得了新进展。

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