Identification of TFB5, a new component of general transcription and DNA repair factor IIH
Open Access
- 27 June 2004
- journal article
- letter
- Published by Springer Nature in Nature Genetics
- Vol. 36 (7), 707-713
- https://doi.org/10.1038/ng1385
Abstract
We previously described the use of quantitative proteomics to study macromolecular complexes1. Applying the method to analyze a yeast RNA polymerase II preinitiation complex, we identified a new 8-kDa protein, encoded by the uncharacterized open reading frame YDR079c-a, as a potential new component of the preinitiation complex. Here we show that YDR079c-a is a bona fide component of polymerase II preinitiation complexes and investigate its role in transcription. YDR079c-a is recruited to promoters both in vivo and in vitro and is required for efficient transcription in vitro and for normal induction of GAL genes. In addition, YDR079c-a is a core component of general transcription and DNA repair factor IIH and is required for efficient recruitment of TFIIH to a promoter. Yeast lacking YDR079c-a grow slowly, and, like strains carrying mutations in core TFIIH subunits, are sensitive to ultraviolet radiation. YDR079c-a is conserved throughout evolution, and mutations in the human ortholog account for a DNA repair–deficient form of the tricothiodystrophy disorder called TTD-A2. The identification of a new, evolutionarily conserved, core TFIIH subunit is essential for our understanding of TFIIH function in transcription, DNA repair and human disease.Keywords
This publication has 27 references indexed in Scilit:
- A new, tenth subunit of TFIIH is responsible for the DNA repair syndrome trichothiodystrophy group ANature Genetics, 2004
- Automated Statistical Analysis of Protein Abundance Ratios from Data Generated by Stable-Isotope Dilution and Tandem Mass SpectrometryAnalytical Chemistry, 2003
- REX1, a Novel Gene Required for DNA RepairJournal of Biological Chemistry, 2003
- The study of macromolecular complexes by quantitative proteomicsNature Genetics, 2003
- Quantitative profiling of differentiation-induced microsomal proteins using isotope-coded affinity tags and mass spectrometryNature Biotechnology, 2001
- Sublimiting concentration of TFIIH transcription/DNA repair factor causes TTD-A trichothiodystrophy disorderNature Genetics, 2000
- Genes For Tfb2, Tfb3, and Tfb4 Subunits of Yeast Transcription/Repair Factor IIHJournal of Biological Chemistry, 1997
- Reconstitution of TFIIH and Requirement of Its DNA Helicase Subunits, Rad3 and Rad25, in the Incision Step of Nucleotide Excision RepairPublished by Elsevier ,1996
- An interaction between the Tfb1 and SsI1 subunits of yeast TFIIH correlates with DNA repair activityNucleic Acids Research, 1995
- Different forms of TFIIH for transcription and DNA repair: Holo-TFIIH and a nucleotide excision repairosomeCell, 1995