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解析抑制作用:共抑制子作用的进化模型。

Deconstructing repression: evolving models of co-repressor action.

机构信息

Department of Medicine, Howard Hughes Medical Institute, School of Medicine, University of California-San Diego, 9500 Gilman Drive, La Jolla, California 92093, USA.

出版信息

Nat Rev Genet. 2010 Feb;11(2):109-23. doi: 10.1038/nrg2736.

Abstract

A crucial aspect of development, homeostasis and prevention of disease is the strict maintenance of patterns of gene repression. Gene repression is largely achieved by the combinatorial action of various enzymatic complexes - known as co-repressor complexes - that are recruited to DNA by transcription factors and often act through enzymatic modification of histone protein tails. Our understanding of how co-repressors act has begun to change over recent years owing to the increased availability of genome-scale data. Here, we consider specific strategies that underlie repression events - for example, those mediated by the nuclear receptor co-repressor (NCoR, also known as NCOR1) and silencing mediator of retinoic acid and thyroid hormone receptor (SMRT, also known as NCOR2) co-repressor complexes - and discuss emerging themes in gene repression.

摘要

基因抑制的严格维持是发育、内稳态和疾病预防的关键方面。基因抑制主要通过各种酶复合物(称为共抑制复合物)的组合作用来实现,这些复合物通过转录因子被招募到 DNA 上,并经常通过组蛋白尾部的酶修饰起作用。近年来,由于基因组规模数据的可用性增加,我们对共抑制因子如何发挥作用的理解开始发生变化。在这里,我们考虑了抑制事件背后的特定策略——例如,由核受体共抑制因子(NCoR,也称为 NCOR1)和视黄酸和甲状腺激素受体沉默介质(SMRT,也称为 NCOR2)共抑制复合物介导的策略——并讨论了基因抑制中出现的主题。

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