Luo Jie, Cimermancic Peter, Viswanath Shruthi, Ebmeier Christopher C, Kim Bong, Dehecq Marine, Raman Vishnu, Greenberg Charles H, Pellarin Riccardo, Sali Andrej, Taatjes Dylan J, Hahn Steven, Ranish Jeff
Institute for Systems Biology, 401 Terry Avenue North, Seattle, WA 98109, USA.
Department of Bioengineering and Therapeutic Sciences, Department of Pharmaceutical Chemistry, California Institute for Quantitative Biomedical Sciences, University of California, San Francisco, San Francisco, CA 94158, USA.
Mol Cell. 2015 Sep 3;59(5):794-806. doi: 10.1016/j.molcel.2015.07.016.
TFIIH is essential for both RNA polymerase II transcription and DNA repair, and mutations in TFIIH can result in human disease. Here, we determine the molecular architecture of human and yeast TFIIH by an integrative approach using chemical crosslinking/mass spectrometry (CXMS) data, biochemical analyses, and previously published electron microscopy maps. We identified four new conserved "topological regions" that function as hubs for TFIIH assembly and more than 35 conserved topological features within TFIIH, illuminating a network of interactions involved in TFIIH assembly and regulation of its activities. We show that one of these conserved regions, the p62/Tfb1 Anchor region, directly interacts with the DNA helicase subunit XPD/Rad3 in native TFIIH and is required for the integrity and function of TFIIH. We also reveal the structural basis for defects in patients with xeroderma pigmentosum and trichothiodystrophy, with mutations found at the interface between the p62 Anchor region and the XPD subunit.
TFIIH对于RNA聚合酶II转录和DNA修复均至关重要,TFIIH中的突变可导致人类疾病。在此,我们通过整合化学交联/质谱(CXMS)数据、生化分析及先前发表的电子显微镜图谱等方法,确定了人类和酵母TFIIH的分子结构。我们识别出四个新的保守“拓扑区域”,它们作为TFIIH组装的枢纽,以及TFIIH内超过35个保守拓扑特征,阐明了TFIIH组装及其活性调节所涉及的相互作用网络。我们表明,这些保守区域之一,即p62/Tfb1锚定区域,在天然TFIIH中直接与DNA解旋酶亚基XPD/Rad3相互作用,并且是TFIIH完整性和功能所必需的。我们还揭示了着色性干皮病和毛发硫营养不良患者缺陷的结构基础,这些患者的突变位于p62锚定区域与XPD亚基之间的界面处。