Hubin Elizabeth A, Fay Allison, Xu Catherine, Bean James M, Saecker Ruth M, Glickman Michael S, Darst Seth A, Campbell Elizabeth A
The Rockefeller University, New York, United States.
Immunology Program, Sloan-Kettering Institute, New York, United States.
Elife. 2017 Jan 9;6:e22520. doi: 10.7554/eLife.22520.
RbpA and CarD are essential transcription regulators in mycobacteria. Mechanistic analyses of promoter open complex (RPo) formation establish that RbpA and CarD cooperatively stimulate formation of an intermediate (RP2) leading to RPo; formation of RP2 is likely a bottleneck step at the majority of mycobacterial promoters. Once RPo forms, CarD also disfavors its isomerization back to RP2. We determined a 2.76 Å-resolution crystal structure of a mycobacterial transcription initiation complex (TIC) with RbpA as well as a CarD/RbpA/TIC model. Both CarD and RbpA bind near the upstream edge of the -10 element where they likely facilitate DNA bending and impede transcription bubble collapse. In vivo studies demonstrate the essential role of RbpA, show the effects of RbpA truncations on transcription and cell physiology, and indicate additional functions for RbpA not evident in vitro. This work provides a framework to understand the control of mycobacterial transcription by RbpA and CarD.
RbpA和CarD是分枝杆菌中至关重要的转录调节因子。对启动子开放复合物(RPo)形成的机制分析表明,RbpA和CarD协同刺激导致RPo的中间体(RP2)的形成;RP2的形成可能是大多数分枝杆菌启动子处的一个瓶颈步骤。一旦RPo形成,CarD也不利于其异构化回到RP2。我们确定了一种含有RbpA的分枝杆菌转录起始复合物(TIC)的2.76 Å分辨率晶体结构以及一个CarD/RbpA/TIC模型。CarD和RbpA都结合在-10元件的上游边缘附近,它们可能在此促进DNA弯曲并阻止转录泡塌陷。体内研究证明了RbpA的重要作用,展示了RbpA截短对转录和细胞生理学的影响,并表明了RbpA在体外不明显的其他功能。这项工作为理解RbpA和CarD对分枝杆菌转录的控制提供了一个框架。