Palangat Murali, Larson Daniel R
Center for Cancer Research, National Cancer Institute, National Institues of Health, Bethesda, MD, USA.
Biochim Biophys Acta. 2012 Jul;1819(7):667-72. doi: 10.1016/j.bbagrm.2012.02.024. Epub 2012 Mar 28.
Transcription of protein-coding genes by RNA polymerase II can be regulated at multiple points during the process of RNA synthesis, including initiation, elongation, and termination. In vivo data suggests that elongating polymerases exhibit heterogeneity throughout the gene body, suggestive of changes in elongation rate and/or pausing. Here, we review evidence from a variety of different experimental approaches for understanding regulation of transcription elongation. We compare steady-state measurements of nascent RNA density and polymerase occupancy to time-resolved measurements and point out areas of disagreement. Finally, we discuss future avenues of investigation for understanding this critically important step in gene regulation. This article is part of a Special Issue entitled: Chromatin in time and space.
RNA聚合酶II对蛋白质编码基因的转录可在RNA合成过程中的多个点受到调控,包括起始、延伸和终止。体内数据表明,延伸中的聚合酶在整个基因体内表现出异质性,这暗示着延伸速率和/或暂停的变化。在这里,我们综述了来自各种不同实验方法的证据,以了解转录延伸的调控。我们将新生RNA密度和聚合酶占据情况的稳态测量与时间分辨测量进行比较,并指出存在分歧的领域。最后,我们讨论了未来的研究途径,以了解基因调控中这一至关重要的步骤。本文是名为:《时空染色质》的特刊的一部分。