Department of Biochemistry, University of Wisconsin-Madison, Madison, United States.
Department of Bacteriology, University of Wisconsin-Madison, Madison, United States.
Elife. 2019 Jan 8;8:e40981. doi: 10.7554/eLife.40981.
Transcriptional pausing underlies regulation of cellular RNA biogenesis. A consensus pause sequence that acts on RNA polymerases (RNAPs) from bacteria to mammals halts RNAP in an elemental paused state from which longer-lived pauses can arise. Although the structural foundations of pauses prolonged by backtracking or nascent RNA hairpins are recognized, the fundamental mechanism of the elemental pause is less well-defined. Here we report a mechanistic dissection that establishes the elemental pause signal () is multipartite; () causes a modest conformational shift that puts γ-proteobacterial RNAP in an off-pathway state in which template base loading but not RNA translocation is inhibited; and () allows RNAP to enter pretranslocated and one-base-pair backtracked states easily even though the half-translocated state observed in paused cryo-EM structures rate-limits pause escape. Our findings provide a mechanistic basis for the elemental pause and a framework to understand how pausing is modulated by sequence, cellular conditions, and regulators.
转录暂停是细胞 RNA 生物发生调控的基础。一个共识暂停序列作用于从细菌到哺乳动物的 RNA 聚合酶(RNAP),将 RNAP 置于基本暂停状态,在这种状态下可以产生更长时间的暂停。尽管已经认识到由回溯或新生 RNA 发夹延长的暂停的结构基础,但基本暂停的基本机制定义得还不够清楚。在这里,我们进行了一项机制剖析,确定了基本暂停信号()是多部分的;()导致适度的构象变化,使 γ-变形菌 RNAP 进入非途径状态,其中模板碱基加载但不抑制 RNA 易位;并且()允许 RNAP 容易地进入预易位和一个碱基回溯的状态,即使在暂停 cryo-EM 结构中观察到的半易位状态限制了暂停逃逸。我们的发现为基本暂停提供了一个机制基础,并为理解暂停如何被序列、细胞条件和调节剂调节提供了一个框架。