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人类干扰素-β基因表达的转录密码。

The transcriptional code of human IFN-beta gene expression.

作者信息

Ford Ethan, Thanos Dimitris

机构信息

Institute of Molecular Biology, Genetics and Biotechnology, Biomedical Research Foundation, Academy of Athens, 4 Soranou Efesiou Street, Athens 11527, Greece.

出版信息

Biochim Biophys Acta. 2010 Mar-Apr;1799(3-4):328-36. doi: 10.1016/j.bbagrm.2010.01.010. Epub 2010 Jan 30.

Abstract

Activation of interferon-beta transcription is a highly ordered process beginning with the delivery of NF-kappaB to the IFN-beta enhancer through a process involving stochastic interchromosomal interactions between the IFN-beta enhancer and specialized Alu elements. NF-kappaB delivery is followed by the binding of ATF-2/c-Jun and IRF proteins in a highly cooperative fashion. The assembled "enhanceosome" then recruits PCAF/GCN5 which acetylates the histone tails of the adjacent nucleosomes. The transcriptional coactivator CBP, which binds in a complex with the RNA polymerase II holoenzyme is recruited by the enhanceosome replacing PCAF/GCN5. Next, SWI/SNF, which is part of the holoenzyme complex, induces a conformational change in a nucleosome positioned over the transcriptional start site allowing TFIID to bind, which promotes the sliding of this nucleosome to a new downstream position. At this point the full pre-initiation complex is assembled and transcription commences. This detailed picture of the IFN-beta transcription program gathered through years of rigorous studies, now serves as a paradigm for understanding complex transcriptional switches in eukaryotic systems.

摘要

干扰素-β转录的激活是一个高度有序的过程,始于通过干扰素-β增强子与特殊Alu元件之间的随机染色体间相互作用,将核因子-κB传递至干扰素-β增强子。核因子-κB传递之后,ATF-2/c-Jun和干扰素调节因子(IRF)蛋白以高度协同的方式结合。组装好的“增强体”随后募集PCAF/GCN5,其可使相邻核小体的组蛋白尾部乙酰化。与RNA聚合酶II全酶结合形成复合物的转录共激活因子CBP被增强体募集,取代PCAF/GCN5。接下来,作为全酶复合物一部分的SWI/SNF诱导位于转录起始位点上方的核小体发生构象变化,从而使TATA盒结合蛋白(TFIID)得以结合,进而促进该核小体滑动至新的下游位置。此时,完整的起始前复合物组装完成,转录开始。通过多年严谨研究得出的这一干扰素-β转录程序的详细图景,如今成为理解真核系统中复杂转录开关的范例。

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