a Division of Hematology , The Children's Hospital of Philadelphia , Philadelphia , PA , USA.
b Perelman School of Medicine , University of Pennsylvania , Philadelphia , PA , USA.
Nucleus. 2016 Jul 3;7(4):1-8. doi: 10.1080/19491034.2016.1200770. Epub 2016 Jul 1.
RNA polymerase 2 (pol2) associates with enhancers and promoters, followed by transcription initiation and subsequent pausing. Upon release, pol2 proceeds into productive elongation. A wide spread view of transcription holds that during elongation, pol2 and associated factors clear the promoter proximal region to track along the chromatin fiber until a termination site is encountered. However, several studies are compatible with alternative models. One common feature among these models is that transcription elongation results from movement of the gene along a complex consisting of pol2 and associated factors. Such a scenario predicts that active enhancers and promoters that are bound by transcription complexes, including pol2 are in dynamic physical proximity with the gene body in a manner paralleling pol2 processivity. This has indeed been observed by chromosome conformation capture under conditions of synchronous transcription. Here we discuss these observations and their implication for architectural models of transcription elongation.
RNA 聚合酶 2(pol2)与增强子和启动子结合,随后进行转录起始和随后的暂停。释放后,pol2 进入有效的延伸阶段。广泛存在的转录观点认为,在延伸过程中,pol2 和相关因子清除启动子近端区域,沿着染色质纤维追踪,直到遇到终止位点。然而,有几项研究与替代模型兼容。这些模型的一个共同特点是,转录延伸是由基因沿着由 pol2 和相关因子组成的复合物的移动产生的。这种情况预测,活跃的增强子和启动子,包括由转录复合物结合的 pol2,与基因体在动态物理接近的方式与 pol2 的持续性平行。这确实是通过同步转录条件下的染色体构象捕获观察到的。在这里,我们讨论这些观察结果及其对转录延伸的结构模型的意义。