Ardehali M Behfar, Yao Jie, Adelman Karen, Fuda Nicholas J, Petesch Steven J, Webb Watt W, Lis John T
Department of Molecular Biology and Genetics, Cornell University, Ithaca, NY 14853, USA.
EMBO J. 2009 Apr 22;28(8):1067-77. doi: 10.1038/emboj.2009.56. Epub 2009 Mar 12.
Several eukaryotic transcription factors have been shown to modulate the elongation rate of RNA polymerase II (Pol II) on naked or chromatin-reconstituted templates in vitro. However, none of the tested factors have been shown to directly affect the elongation rate of Pol II in vivo. We performed a directed RNAi knock-down (KD) screen targeting 141 candidate transcription factors and identified multiple factors, including Spt6, that alter the induced Hsp70 transcript levels in Drosophila S2 cells. Spt6 is known to interact with both nucleosome structure and Pol II, and it has properties consistent with having a role in elongation. Here, ChIP assays of the first wave of Pol II after heat shock in S2 cells show that KD of Spt6 reduces the rate of Pol II elongation. Also, fluorescence recovery after photobleaching assays of GFP-Pol II in salivary gland cells show that this Spt6-dependent effect on elongation rate persists during steady-state-induced transcription, reducing the elongation rate from approximately 1100 to 500 bp/min. Furthermore, RNAi depletion of Spt6 reveals its broad requirement during different stages of development.
已有研究表明,几种真核转录因子可在体外调节RNA聚合酶II(Pol II)在裸露或染色质重构模板上的延伸速率。然而,在体内尚未有实验证明所测试的转录因子能直接影响Pol II的延伸速率。我们针对141个候选转录因子进行了定向RNA干扰敲除(KD)筛选,并鉴定出多个能够改变果蝇S2细胞中热休克蛋白70(Hsp70)转录本诱导水平的因子,其中包括Spt6。已知Spt6与核小体结构和Pol II均有相互作用,并且其特性表明它在延伸过程中发挥作用。在此,对S2细胞热休克后首批Pol II进行的染色质免疫沉淀(ChIP)分析表明,Spt6的敲除降低了Pol II的延伸速率。此外,对唾液腺细胞中绿色荧光蛋白标记的Pol II(GFP-Pol II)进行的光漂白后荧光恢复分析表明,在稳态诱导转录过程中,Spt6对延伸速率的影响依然存在,延伸速率从约1100 bp/min降至500 bp/min。此外,RNA干扰去除Spt6后揭示了其在发育不同阶段的广泛需求。