Dollinger Roberta, Deng Eilene B, Schultz Josie, Wu Sharon, Deorio Haley R, Gilmour David S
Center for Eukaryotic Gene Regulation, Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, Pennsylvania, USA.
Center for Eukaryotic Gene Regulation, Department of Biochemistry and Molecular Biology, Pennsylvania State University, University Park, Pennsylvania, USA; Department of Biomolecular Chemistry, University of Wisconsin-Madison, Madison, Wisconsin, USA.
J Biol Chem. 2023 Sep;299(9):105106. doi: 10.1016/j.jbc.2023.105106. Epub 2023 Jul 28.
Promoter proximal pausing of RNA polymerase II (Pol II) is a critical transcriptional regulatory mechanism in metazoans that requires the transcription factor DRB sensitivity-inducing factor (DSIF) and the inhibitory negative elongation factor (NELF). DSIF, composed of Spt4 and Spt5, establishes the pause by recruiting NELF to the elongation complex. However, the role of DSIF in pausing beyond NELF recruitment remains unclear. We used a highly purified in vitro system and Drosophila nuclear extract to investigate the role of DSIF in promoter proximal pausing. We identified two domains of Spt5, the KOW4 and NGN domains, that facilitate Pol II pausing. The KOW4 domain promotes pausing through its interaction with the nascent RNA while the NGN domain does so through a short helical motif that is in close proximity to the non-transcribed DNA template strand. Removal of this sequence in Drosophila has a male-specific dominant negative effect. The alpha-helical motif is also needed to support fly viability. We also show that the interaction between the Spt5 KOW1 domain and the upstream DNA helix is required for DSIF association with the Pol II elongation complex. Disruption of the KOW1-DNA interaction is dominant lethal in vivo. Finally, we show that the KOW2-3 domain of Spt5 mediates the recruitment of NELF to the elongation complex. In summary, our results reveal additional roles for DSIF in transcription regulation and identify specific domains important for facilitating Pol II pausing.
RNA聚合酶II(Pol II)在启动子近端的暂停是后生动物中一种关键的转录调控机制,这一过程需要转录因子DRB敏感性诱导因子(DSIF)和抑制性负向延伸因子(NELF)。由Spt4和Spt5组成的DSIF通过将NELF招募到延伸复合物来建立暂停。然而,DSIF在NELF招募之外的暂停过程中的作用仍不清楚。我们使用了高度纯化的体外系统和果蝇核提取物来研究DSIF在启动子近端暂停中的作用。我们鉴定出Spt5的两个结构域,即KOW4和NGN结构域,它们有助于Pol II的暂停。KOW4结构域通过与新生RNA相互作用促进暂停,而NGN结构域则通过靠近非转录DNA模板链的短螺旋基序来实现这一功能。在果蝇中去除该序列会产生雄性特异性的显性负效应。这个α-螺旋基序对于维持果蝇的生存能力也是必需的。我们还表明,Spt5的KOW1结构域与上游DNA螺旋之间的相互作用是DSIF与Pol II延伸复合物结合所必需的。破坏KOW1与DNA的相互作用在体内是显性致死的。最后,我们证明Spt5的KOW2 - 3结构域介导了NELF向延伸复合物的招募。总之,我们的结果揭示了DSIF在转录调控中的其他作用,并确定了对促进Pol II暂停很重要的特定结构域。