Department of Biochemistry and Molecular Biology, University of Texas Medical Branch at Galveston, Galveston, TX 77550, USA.
Department of Biological Chemistry and Molecular Pharmacology, Harvard Medical School, Boston, MA 02115, USA.
Mol Cell. 2020 Oct 15;80(2):345-358.e9. doi: 10.1016/j.molcel.2020.08.016. Epub 2020 Sep 22.
Efficient release of promoter-proximally paused RNA Pol II into productive elongation is essential for gene expression. Recently, we reported that the Integrator complex can bind paused RNA Pol II and drive premature transcription termination, potently attenuating the activity of target genes. Premature termination requires RNA cleavage by the endonuclease subunit of Integrator, but the roles of other Integrator subunits in gene regulation have yet to be elucidated. Here we report that Integrator subunit 8 (IntS8) is critical for transcription repression and required for association with protein phosphatase 2A (PP2A). We find that Integrator-bound PP2A dephosphorylates the RNA Pol II C-terminal domain and Spt5, preventing the transition to productive elongation. Thus, blocking PP2A association with Integrator stimulates pause release and gene activity. These results reveal a second catalytic function associated with Integrator-mediated transcription termination and indicate that control of productive elongation involves active competition between transcriptional kinases and phosphatases.
促进 RNA 聚合酶 II 从起始延伸复合物中有效释放到延伸阶段对于基因表达至关重要。最近,我们报道了整合酶复合物可以结合起始延伸复合物中的 RNA 聚合酶 II,并驱动转录过早终止,从而强烈抑制靶基因的活性。过早终止需要整合酶的内切核酸酶亚基进行 RNA 切割,但整合酶其他亚基在基因调控中的作用尚未阐明。在这里,我们报告整合酶亚基 8(IntS8)对于转录抑制是至关重要的,并且需要与蛋白磷酸酶 2A(PP2A)结合。我们发现整合酶结合的 PP2A 可以使 RNA 聚合酶 II C 末端结构域和 Spt5 去磷酸化,从而阻止向延伸阶段的转变。因此,阻止 PP2A 与整合酶的结合可以刺激暂停释放和基因活性。这些结果揭示了与整合酶介导的转录终止相关的第二个催化功能,并表明延伸阶段的控制涉及转录激酶和磷酸酶之间的积极竞争。