C Quaresma Alexandre J, Bugai Andrii, Barboric Matjaz
Medicum, Department of Biochemistry and Developmental Biology, University of Helsinki, Helsinki FIN-00014, Finland.
Medicum, Department of Biochemistry and Developmental Biology, University of Helsinki, Helsinki FIN-00014, Finland
Nucleic Acids Res. 2016 Sep 19;44(16):7527-39. doi: 10.1093/nar/gkw585. Epub 2016 Jul 1.
Release of RNA polymerase II (Pol II) from promoter-proximal pausing has emerged as a critical step regulating gene expression in multicellular organisms. The transition of Pol II into productive elongation requires the kinase activity of positive transcription elongation factor b (P-TEFb), which is itself under a stringent control by the inhibitory 7SK small nuclear ribonucleoprotein (7SK snRNP) complex. Here, we provide an overview on stimulating Pol II pause release by P-TEFb and on sequestering P-TEFb into 7SK snRNP. Furthermore, we highlight mechanisms that govern anchoring of 7SK snRNP to chromatin as well as means that release P-TEFb from the inhibitory complex, and propose a unifying model of P-TEFb activation on chromatin. Collectively, these studies shine a spotlight on the central role of RNA binding proteins (RBPs) in directing the inhibition and activation of P-TEFb, providing a compelling paradigm for controlling Pol II transcription with a non-coding RNA.
RNA聚合酶II(Pol II)从启动子近端暂停状态的释放已成为多细胞生物中调节基因表达的关键步骤。Pol II向有效延伸的转变需要正转录延伸因子b(P-TEFb)的激酶活性,而P-TEFb本身受到抑制性7SK小核核糖核蛋白(7SK snRNP)复合物的严格调控。在此,我们概述了P-TEFb刺激Pol II暂停释放以及将P-TEFb隔离到7SK snRNP中的情况。此外,我们强调了控制7SK snRNP锚定到染色质的机制以及将P-TEFb从抑制复合物中释放出来的方式,并提出了染色质上P-TEFb激活的统一模型。总的来说,这些研究突出了RNA结合蛋白(RBP)在指导P-TEFb抑制和激活方面的核心作用,为用非编码RNA控制Pol II转录提供了一个令人信服的范例。