Pascual-García Pau, Govind Chhabi K, Queralt Ethel, Cuenca-Bono Bernardo, Llopis Ana, Chavez Sebastián, Hinnebusch Alan G, Rodríguez-Navarro Susana
Centro de Investigación Príncipe Felipe, E-46012 Valencia, Spain.
Genes Dev. 2008 Oct 15;22(20):2811-22. doi: 10.1101/gad.483308.
Gene transcription, RNA biogenesis, and mRNA transport constitute a complicated process essential for all eukaryotic cells. The transcription/export factor Sus1 plays a key role in coupling transcription activation with mRNA export, and it resides in both the SAGA and TREX2 complexes. Moreover, Sus1 is responsible for GAL1 gene gating at the nuclear periphery, which is important for its transcriptional status. Here, we show that Sus1 is required during transcription elongation and is associated with the elongating form of RNA Polymerase II (RNAP II) phosphorylated on Ser5 and Ser2 of the C-terminal domain (CTD). In addition, Sus1 copurifies with the essential mRNA export factors Yra1 and Mex67, which bind to the mRNA cotranscriptionally. Consistently, ChIP analysis reveals that Sus1 is present at coding regions dependent on transcription in a manner stimulated by Kin28-dependent CTD phosphorylation. Strikingly, eliminating the TREX2 component Sac3 or the SAGA subunit Ubp8 partially impairs Sus1 targeting to coding sequences and upstream activating sequences (UAS). We found, unexpectedly, that Sgf73 is necessary for association of Sus1 with both SAGA and TREX2, and that its absence dramatically reduces Sus1 occupancy of UAS and ORF sequences. Our results reveal that Sus1 plays a key role in coordinating gene transcription and mRNA export by working at the interface between the SAGA and TREX2 complexes during transcription elongation.
基因转录、RNA生物合成和mRNA转运构成了所有真核细胞所必需的复杂过程。转录/输出因子Sus1在将转录激活与mRNA输出偶联中起关键作用,它存在于SAGA和TREX2复合物中。此外,Sus1负责GAL1基因在核周边的门控,这对其转录状态很重要。在这里,我们表明Sus1在转录延伸过程中是必需的,并且与在C末端结构域(CTD)的Ser5和Ser2位点磷酸化的RNA聚合酶II(RNAP II)的延伸形式相关联。此外,Sus1与必需的mRNA输出因子Yra1和Mex67共纯化,它们在转录过程中与mRNA结合。一致地,ChIP分析表明Sus1以依赖于Kin28的CTD磷酸化刺激的方式存在于依赖转录的编码区域。令人惊讶的是,消除TREX2组分Sac3或SAGA亚基Ubp8会部分损害Sus1靶向编码序列和上游激活序列(UAS)。我们意外地发现,Sgf73对于Sus1与SAGA和TREX2的结合是必需的,并且其缺失会显著降低Sus1在UAS和ORF序列上的占据率。我们的结果表明,Sus1在转录延伸过程中通过在SAGA和TREX2复合物之间的界面起作用,在协调基因转录和mRNA输出中起关键作用。