Gilchrist Daniel A, Adelman Karen
Laboratory of Molecular Carcinogenesis, National Institute of Environmental Health Sciences, NIH, Research Triangle Park, NC 27709, USA.
Biochim Biophys Acta. 2012 Jul;1819(7):700-6. doi: 10.1016/j.bbagrm.2012.02.015. Epub 2012 Mar 2.
Altering gene expression in response to stimuli is a pivotal mechanism through which organisms execute developmental programs and respond to changes in their environment. Packaging of promoter DNA into chromatin can greatly impact the ability of RNA polymerase II to access and transcribe a gene. Promoter chromatin environments thus play a central role in establishing transcriptional output appropriate for specific environmental conditions or developmental states. Recent genomic studies have illuminated general principles of chromatin organization and deepened our understanding of how promoter sequence and nucleosome architecture may impact gene expression. Concurrently, pausing of polymerase during early elongation has been recognized as an important event influencing transcription of genes within stimulus-responsive networks. Promoters regulated by pausing are now recognized to possess a distinct chromatin architecture that may facilitate the plasticity of gene expression in response to signaling events. Here we review advances in understanding chromatin and pausing, and explore how coupling Pol II pausing to distinct promoter architectures may help organisms achieve flexible yet precise transcriptional control. This article is part of a Special Issue entitled: Chromatin in time and space.
响应刺激而改变基因表达是生物体执行发育程序并应对环境变化的关键机制。启动子DNA包装成染色质会极大地影响RNA聚合酶II访问和转录基因的能力。因此,启动子染色质环境在建立适合特定环境条件或发育状态的转录输出方面起着核心作用。最近的基因组研究揭示了染色质组织的一般原则,并加深了我们对启动子序列和核小体结构如何影响基因表达的理解。同时,聚合酶在早期延伸过程中的暂停已被认为是影响刺激响应网络内基因转录的重要事件。现在人们认识到,受暂停调节的启动子具有独特的染色质结构,这可能有助于基因表达响应信号事件的可塑性。在这里,我们综述了在理解染色质和暂停方面的进展,并探讨了将Pol II暂停与不同的启动子结构相结合如何帮助生物体实现灵活而精确的转录控制。本文是名为:《时空染色质》的特刊的一部分。