The transcription factor IID subunit Taf13 is dispensable for TATA binding protein promoter recruitment and RNA polymerase II transcription

IF 4.6 2区 综合性期刊 Q1 MULTIDISCIPLINARY SCIENCES
Igor Martianov , Stephanie Le Gras , Guillaume Davidson , Irwin Davidson
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引用次数: 0

Abstract

The multiprotein complex TFIID, comprising the TATA binding protein (TBP) and 13 TBP-associated factors (TAFs), is an essential component of the RNA polymerase II (Pol II) preinitiation complex (PIC). Cryo-electron microscopy studies suggested a critical role of the TAF11-TAF13 heterodimer in TBP promoter deposition upstream of the transcription start site. To investigate this hypothesis, we inactivated the gene encoding Taf13 in mice and embryonic stem cells (ESCs). Taf13-null embryos implant and survive until E6.5, but fail to undergo gastrulation, while Taf13-null ESCs are viable, but fail to form embryoid bodies and differentiate. Taf13 loss had little effect on TFIID integrity and led to only a mild reduction of TBP promoter recruitment, but led to altered PIC formation and globally reduced Pol II recruitment. Thus, the Taf11-Taf13 heterodimer is not essential for TBP/TFIID recruitment, revealing plasticity in the pathways of PIC formation.
转录因子IID亚基Taf13对于TATA结合蛋白启动子募集和RNA聚合酶II转录是必不可少的
多蛋白复合物TFIID由TATA结合蛋白(TBP)和13个TBP相关因子(TAFs)组成,是RNA聚合酶II (Pol II)预起始复合物(PIC)的重要组成部分。低温电镜研究表明,TAF11-TAF13异源二聚体在转录起始位点上游的TBP启动子沉积中起着关键作用。为了验证这一假说,我们在小鼠和胚胎干细胞(ESCs)中灭活了编码Taf13的基因。Taf13-null胚胎植入并存活至E6.5,但不能发生原肠胚形成,而Taf13-null胚胎可存活,但不能形成胚状体并分化。Taf13缺失对TFIID完整性的影响很小,仅导致TBP启动子招募轻微减少,但导致PIC形成改变和全局Pol II招募减少。因此,Taf11-Taf13异源二聚体对于TBP/TFIID的募集并不是必需的,这揭示了PIC形成途径的可塑性。
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来源期刊
iScience
iScience Multidisciplinary-Multidisciplinary
CiteScore
7.20
自引率
1.70%
发文量
1972
审稿时长
6 weeks
期刊介绍: Science has many big remaining questions. To address them, we will need to work collaboratively and across disciplines. The goal of iScience is to help fuel that type of interdisciplinary thinking. iScience is a new open-access journal from Cell Press that provides a platform for original research in the life, physical, and earth sciences. The primary criterion for publication in iScience is a significant contribution to a relevant field combined with robust results and underlying methodology. The advances appearing in iScience include both fundamental and applied investigations across this interdisciplinary range of topic areas. To support transparency in scientific investigation, we are happy to consider replication studies and papers that describe negative results. We know you want your work to be published quickly and to be widely visible within your community and beyond. With the strong international reputation of Cell Press behind it, publication in iScience will help your work garner the attention and recognition it merits. Like all Cell Press journals, iScience prioritizes rapid publication. Our editorial team pays special attention to high-quality author service and to efficient, clear-cut decisions based on the information available within the manuscript. iScience taps into the expertise across Cell Press journals and selected partners to inform our editorial decisions and help publish your science in a timely and seamless way.
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