Das Rita, Yu Jiong, Zhang Zuo, Gygi Melanie P, Krainer Adrian R, Gygi Steven P, Reed Robin
Department of Cell Biology, Harvard Medical School, 240 Longwood Avenue, Boston, MA 02115, USA.
Mol Cell. 2007 Jun 22;26(6):867-81. doi: 10.1016/j.molcel.2007.05.036.
Transcription and splicing are functionally coupled, resulting in highly efficient splicing of RNA polymerase II (RNAP II) transcripts. The mechanism involved in this coupling is not known. To identify potential coupling factors, we carried out a comprehensive proteomic analysis of immunopurified human RNAP II, identifying >100 specifically associated proteins. Among these are the SR protein family of splicing factors and all of the components of U1 snRNP, but no other snRNPs or splicing factors. We show that SR proteins function in coupling transcription to splicing and provide evidence that the mechanism involves cotranscriptional recruitment of SR proteins to RNAP II transcripts. We propose that the exclusive association of U1 snRNP/SR proteins with RNAP II positions these splicing factors, which are known to function early in spliceosome assembly, close to the nascent pre-mRNA. Thus, these factors readily out-compete inhibitory hnRNP proteins, resulting in efficient spliceosome assembly on nascent RNAP II transcripts.
转录与剪接在功能上相互偶联,使得RNA聚合酶II(RNAP II)转录本能够高效剪接。这种偶联所涉及的机制尚不清楚。为了鉴定潜在的偶联因子,我们对免疫纯化的人RNAP II进行了全面的蛋白质组学分析,鉴定出100多种特异性相关蛋白。其中包括剪接因子的SR蛋白家族以及U1 snRNP的所有组分,但没有其他snRNP或剪接因子。我们表明SR蛋白在转录与剪接的偶联中发挥作用,并提供证据表明该机制涉及SR蛋白共转录募集至RNAP II转录本。我们提出U1 snRNP/SR蛋白与RNAP II的排他性结合将这些已知在剪接体组装早期发挥作用的剪接因子定位在新生前体mRNA附近。因此,这些因子很容易在竞争中胜过抑制性hnRNP蛋白,从而在新生的RNAP II转录本上实现高效的剪接体组装。