Literature DB >> 8465201

DNA repair helicase: a component of BTF2 (TFIIH) basic transcription factor.

L Schaeffer1, R Roy, S Humbert, V Moncollin, W Vermeulen, J H Hoeijmakers, P Chambon, J M Egly.   

Abstract

The human BTF2 basic transcription factor (also called TFIIH), which is similar to the delta factor in rat and factor b in yeast, is required for class II gene transcription. A strand displacement assay was used to show that highly purified preparation of BTF2 had an adenosine triphosphate-dependent DNA helicase activity, in addition to the previously characterized carboxyl-terminal domain kinase activity. Amino acid sequence analysis of the tryptic digest generated from the 89-kilodalton subunit of BTF2 indicated that this polypeptide corresponded to the ERCC-3 gene product, a presumed helicase implicated in the human DNA excision repair disorders xeroderma pigmentosum and Cockayne's syndrome. These findings suggest that transcription and nucleotide excision repair may share common factors and hence may be considered to be functionally related.

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Year:  1993        PMID: 8465201     DOI: 10.1126/science.8465201

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  235 in total

1.  Mixed spermatogenic germ cell nuclear extracts exhibit high base excision repair activity.

Authors:  G W Intano; C A McMahan; R B Walter; J R McCarrey; C A Walter
Journal:  Nucleic Acids Res       Date:  2001-03-15       Impact factor: 16.971

2.  A multistep damage recognition mechanism for global genomic nucleotide excision repair.

Authors:  K Sugasawa; T Okamoto; Y Shimizu; C Masutani; S Iwai; F Hanaoka
Journal:  Genes Dev       Date:  2001-03-01       Impact factor: 11.361

3.  Molecular characterization of mutant alleles of the DNA repair/basal transcription factor haywire/ERCC3 in Drosophila.

Authors:  L C Mounkes; M T Fuller
Journal:  Genetics       Date:  1999-05       Impact factor: 4.562

4.  The general transcription factors IIA, IIB, IIF, and IIE are required for RNA polymerase II transcription from the human U1 small nuclear RNA promoter.

Authors:  T C Kuhlman; H Cho; D Reinberg; N Hernandez
Journal:  Mol Cell Biol       Date:  1999-03       Impact factor: 4.272

5.  Gadd45, a p53-responsive stress protein, modifies DNA accessibility on damaged chromatin.

Authors:  F Carrier; P T Georgel; P Pourquier; M Blake; H U Kontny; M J Antinore; M Gariboldi; T G Myers; J N Weinstein; Y Pommier; A J Fornace
Journal:  Mol Cell Biol       Date:  1999-03       Impact factor: 4.272

6.  Cell cycle-independent removal of UV-induced pyrimidine dimers from the promoter and the transcription initiation domain of the human CDC2 gene.

Authors:  S Tommasi; A B Oxyzoglou; G P Pfeifer
Journal:  Nucleic Acids Res       Date:  2000-10-15       Impact factor: 16.971

7.  Molecular cloning of a cDNA encoding mouse DNA helicase B, which has homology to Escherichia coli RecD protein, and identification of a mutation in the DNA helicase B from tsFT848 temperature-sensitive DNA replication mutant cells.

Authors:  S Tada; T Kobayashi; A Omori; Y Kusa; N Okumura; H Kodaira; Y Ishimi; M Seki; T Enomoto
Journal:  Nucleic Acids Res       Date:  2001-09-15       Impact factor: 16.971

Review 8.  Navigating the nucleotide excision repair threshold.

Authors:  Liren Liu; Jennifer Lee; Pengbo Zhou
Journal:  J Cell Physiol       Date:  2010-09       Impact factor: 6.384

9.  Transitions in the coupling of transcription and nucleotide excision repair within RNA polymerase II-transcribed genes of Saccharomyces cerevisiae.

Authors:  M Tijsterman; R A Verhage; P van de Putte; J G Tasseron-de Jong; J Brouwer
Journal:  Proc Natl Acad Sci U S A       Date:  1997-07-22       Impact factor: 11.205

10.  Reduced RNA polymerase II transcription in extracts of cockayne syndrome and xeroderma pigmentosum/Cockayne syndrome cells.

Authors:  G L Dianov; J F Houle; N Iyer; V A Bohr; E C Friedberg
Journal:  Nucleic Acids Res       Date:  1997-09-15       Impact factor: 16.971

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