Reeves Wendy M, Hahn Steven
Molecular and Cellular Biology Program, University of Washington, Seattle 98105, USA.
Mol Cell Biol. 2003 Jan;23(1):349-58. doi: 10.1128/MCB.23.1.349-358.2003.
RNA polymerase II (Pol II) Mediator plays an essential role in both basal and activated transcription. Previously, subunits of the Sin4 Mediator complex (Sin4, Pgd1, Gal11, and Med2) have been implicated in both positive and negative transcriptional regulation. Furthermore, it was proposed that this subcomplex constitutes an activator-binding domain. A yeast nuclear-extract system was used to investigate the biochemical role of the Sin4 complex. In contrast to previous findings, we found at least two general activator-independent roles for the Sin4 complex. First, mutations in sin4 and pgd1 destabilized the Pol II-Med complex, leading to a reduced rate and extent of preinitiation complex (PIC) formation both in the presence and absence of activators. Although reduced in amount compared with the wild type, PICs that are formed lacking the Sin4 complex are stable and can initiate transcription normally. Second, mutation of pgd1 causes partial disruption of the Sin4 complex and leads to a defect in transcription reinitiation. This defect is caused by dissociation of mutant Mediator from promoters after initiation, leading to nonfunctional Scaffold complexes. These results show that function of the Sin4 complex is not essential for transcription activation in a crude in vitro system but that it plays key roles in the general transcription mechanism.
RNA聚合酶II(Pol II)中介体在基础转录和激活转录中都起着至关重要的作用。此前,Sin4中介体复合物的亚基(Sin4、Pgd1、Gal11和Med2)已被证明与正向和负向转录调控有关。此外,有人提出这个亚复合物构成一个激活剂结合结构域。我们使用酵母核提取物系统来研究Sin4复合物的生化作用。与之前的研究结果相反,我们发现Sin4复合物至少有两个不依赖于一般激活剂的作用。首先,sin4和pgd1中的突变使Pol II-中介体复合物不稳定,导致在有和没有激活剂的情况下,起始前复合物(PIC)形成的速率和程度降低。虽然与野生型相比数量减少,但在没有Sin4复合物的情况下形成的PIC是稳定的,并且能够正常起始转录。其次,pgd1的突变导致Sin4复合物部分破坏,并导致转录重新起始缺陷。这种缺陷是由起始后突变型中介体从启动子上解离引起的,导致支架复合物失去功能。这些结果表明,在一个粗制的体外系统中,Sin4复合物的功能对于转录激活不是必需的,但它在一般转录机制中起着关键作用。