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.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4560838PMC
http://dx.doi.org/10.1016/j.molcel.2015.07.016DOI Listing

Publication Analysis

Top Keywords

tfiih
9
architecture human
8
human yeast
8
transcription dna
8
dna repair
8
tfiih assembly
8
anchor region
8
yeast general
4
general transcription
4
repair factor
4

Similar Publications

Background: Platinum chemotherapy (CT) remains the backbone of systemic therapy for patients with small-cell lung cancer (SCLC). The nucleotide excision repair (NER) pathway plays a central role in the repair of the DNA damage exerted by platinum agents. Alteration in this repair mechanism may affect patients' survival.

View Article and Find Full Text PDF

Unlocking transcription-coupled DNA repair with the STK19 key.

Mol Cell

December 2024

Department of Pharmacology and Chemical Biology, University of Pittsburgh School of Medicine, Pittsburgh, PA, USA; UPMC-Hillman Cancer Center, Pittsburgh, PA, USA. Electronic address:

A study in Molecular Cell by Ramadhin et al. and two studies in Cell by van den Heuvel et al. and by Mevissen et al.

View Article and Find Full Text PDF

Transcription-coupled repair - mechanisms of action, regulation, and associated human disorders.

FEBS Lett

December 2024

Department of Genetics, Research Institute of Environmental Medicine (RIeM), Nagoya University, Furo-cho, Chikusa-ku, Nagoya, 464-8601, Japan.

The transcription-coupled repair (TCR) pathway resolves transcription-blocking DNA lesions to maintain cellular function and prevent transcriptional arrest. Stalled RNA polymerase II (RNAPII) triggers repair mechanisms, including RNAPII ubiquitination, which recruit UVSSA and TFIIH. Defects in TCR-associated genes cause disorders like Cockayne syndrome, UV-sensitive syndrome, xeroderma pigmentosum, and recently defined AMeDS.

View Article and Find Full Text PDF
Article Synopsis
  • Human Excision Repair Cross-Complementation Group 2 (ERCC2) proteins are crucial for the nucleotide excision repair pathway, and polymorphisms in the ERCC2 gene are linked to cancer susceptibility, though previous findings were inconsistent.
  • This study aimed to explore the connection between specific ERCC2 genetic polymorphisms at codons 312 and 751 and the risk and aggressiveness of bladder cancer in Bangladeshi patients.
  • Results indicated that individuals with certain ERCC2 polymorphisms, particularly Gln/Gln at codon 751 and Asp/Asn at codon 312, had a significantly higher risk of developing bladder cancer, especially among those with a family history of the disease.
View Article and Find Full Text PDF

Transcription-coupled DNA repair (TCR) removes bulky DNA lesions impeding RNA polymerase II (RNAPII) transcription. Recent studies have outlined the stepwise assembly of TCR factors CSB, CSA, UVSSA, and transcription factor IIH (TFIIH) around lesion-stalled RNAPII. However, the mechanism and factors required for the transition to downstream repair steps, including RNAPII removal to provide repair proteins access to the DNA lesion, remain unclear.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!