| Literature DB >> 26340423 |
Jie Luo1, Peter Cimermancic2, Shruthi Viswanath2, Christopher C Ebmeier3, Bong Kim1, Marine Dehecq4, Vishnu Raman3, Charles H Greenberg2, Riccardo Pellarin2, Andrej Sali2, Dylan J Taatjes3, Steven Hahn5, Jeff Ranish6.
Abstract
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.Entities:
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Year: 2015 PMID: 26340423 PMCID: PMC4560838 DOI: 10.1016/j.molcel.2015.07.016
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970