Department of Hematology, Medical Research Institute, Frontier Science Center for Immunology and Metabolism, Zhongnan Hospital of Wuhan University, Wuhan University, Wuhan, China.
TaiKang Center for Life and Medical Sciences, Wuhan University, Wuhan, China.
Genome Biol. 2024 Apr 19;25(1):102. doi: 10.1186/s13059-024-03242-6.
Splicing factors are vital for the regulation of RNA splicing, but some have also been implicated in regulating transcription. The underlying molecular mechanisms of their involvement in transcriptional processes remain poorly understood.
Here, we describe a direct role of splicing factor RBM22 in coordinating multiple steps of RNA Polymerase II (RNAPII) transcription in human cells. The RBM22 protein widely occupies the RNAPII-transcribed gene locus in the nucleus. Loss of RBM22 promotes RNAPII pause release, reduces elongation velocity, and provokes transcriptional readthrough genome-wide, coupled with production of transcripts containing sequences from downstream of the gene. RBM22 preferentially binds to the hyperphosphorylated, transcriptionally engaged RNAPII and coordinates its dynamics by regulating the homeostasis of the 7SK-P-TEFb complex and the association between RNAPII and SPT5 at the chromatin level.
Our results uncover the multifaceted role of RBM22 in orchestrating the transcriptional program of RNAPII and provide evidence implicating a splicing factor in both RNAPII elongation kinetics and termination control.
剪接因子对于 RNA 剪接的调控至关重要,但有些因子也被牵涉到转录调控中。它们参与转录过程的潜在分子机制仍知之甚少。
在这里,我们描述了剪接因子 RBM22 在协调人类细胞中 RNA 聚合酶 II(RNAPII)转录的多个步骤中的直接作用。RBM22 蛋白广泛占据核内 RNAPII 转录基因座。RBM22 的缺失促进了 RNAPII 暂停释放,降低了延伸速度,并在全基因组范围内引发转录通读,同时产生包含基因下游序列的转录本。RBM22 优先结合高度磷酸化的、转录活跃的 RNAPII,并通过调节 7SK-P-TEFb 复合物的动态平衡以及 RNAPII 和 SPT5 在染色质水平上的结合来协调其动力学。
我们的结果揭示了 RBM22 在协调 RNAPII 转录程序中的多方面作用,并提供了证据表明剪接因子既参与 RNAPII 延伸动力学,也参与终止控制。