Department of Cell Biology and Molecular Genetics, The University of Maryland, College Park, MD 20742.
Microbiol Spectr. 2018 Sep;6(5). doi: 10.1128/microbiolspec.RWR-0031-2018.
Transcription is a discontinuous process, where each nucleotide incorporation cycle offers a decision between elongation, pausing, halting, or termination. Many -acting regulatory RNAs, such as riboswitches, exert their influence over transcription elongation. Through such mechanisms, certain RNA elements can couple physiological or environmental signals to transcription attenuation, a process where -acting regulatory RNAs directly influence formation of transcription termination signals. However, through another regulatory mechanism called processive antitermination (PA), RNA polymerase can bypass termination sites over much greater distances than transcription attenuation. PA mechanisms are widespread in bacteria, although only a few classes have been discovered overall. Also, although traditional, signal-responsive riboswitches have not yet been discovered to promote PA, it is increasingly clear that small RNA elements are still oftentimes required. In some instances, small RNA elements serve as loading sites for cellular factors that promote PA. In other instances, larger, more complicated RNA elements participate in PA in unknown ways, perhaps even acting alone to trigger PA activity. These discoveries suggest that what is now needed is a systematic exploration of PA in bacteria, to determine how broadly these transcription elongation mechanisms are utilized, to reveal the diversity in their molecular mechanisms, and to understand the general logic behind their cellular applications. This review covers the known examples of PA regulatory mechanisms and speculates that they may be broadly important to bacteria.
转录是一个不连续的过程,其中每个核苷酸掺入循环提供了延伸、暂停、停止或终止之间的选择。许多多效调节 RNA,如核糖体开关,对转录延伸发挥其影响。通过这种机制,某些 RNA 元件可以将生理或环境信号与转录衰减耦合,其中多效调节 RNA 直接影响转录终止信号的形成。然而,通过另一种称为连续抗终止(PA)的调节机制,RNA 聚合酶可以绕过终止位点,比转录衰减远得多。PA 机制在细菌中广泛存在,尽管总体上只发现了少数几类。此外,尽管传统的、响应信号的核糖体开关尚未被发现促进 PA,但越来越清楚的是,小 RNA 元件通常仍然是必需的。在某些情况下,小 RNA 元件作为促进 PA 的细胞因子的加载位点。在其他情况下,更大、更复杂的 RNA 元件以未知的方式参与 PA,甚至可能单独触发 PA 活性。这些发现表明,现在需要对细菌中的 PA 进行系统探索,以确定这些转录延伸机制被广泛利用的程度,揭示它们在分子机制上的多样性,并理解其在细胞应用中的一般逻辑。这篇综述涵盖了已知的 PA 调节机制的例子,并推测它们可能对细菌广泛重要。