Literature DB >> 7920640

Mutations in the xeroderma pigmentosum group D DNA repair/transcription gene in patients with trichothiodystrophy.

B C Broughton1, H Steingrimsdottir, C A Weber, A R Lehmann.   

Abstract

DNA repair defects in the xeroderma pigmentosum (XP) group D complementation group can be associated with the clinical features of two quite different disorders; XP, a sun-sensitive and cancer-prone disorder, or trichothiodystrophy (TTD) which is characterized by sulphur-deficient brittle hair and a variety of other associated abnormalities, but no skin cancer. The XPD gene product, a DNA helicase, is required for nucleotide excision repair and recent evidence has demonstrated a role in transcription. We have now identified causative mutations in XPD in four TTD patients. The patients are all compound heterozygotes and the locations of the mutations enable us to suggest relationships between different domains in the gene and its roles in excision repair and transcription.

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Year:  1994        PMID: 7920640     DOI: 10.1038/ng0694-189

Source DB:  PubMed          Journal:  Nat Genet        ISSN: 1061-4036            Impact factor:   38.330


  29 in total

1.  Domain structure, localization, and function of DNA polymerase eta, defective in xeroderma pigmentosum variant cells.

Authors:  P Kannouche; B C Broughton; M Volker; F Hanaoka; L H Mullenders; A R Lehmann
Journal:  Genes Dev       Date:  2001-01-15       Impact factor: 11.361

2.  Diagnosis of Xeroderma Pigmentosum and Related DNA Repair-Deficient Cutaneous Diseases.

Authors:  James E Cleaver
Journal:  Curr Med Lit Dermatol       Date:  2008

Review 3.  Trichothiodystrophy: a systematic review of 112 published cases characterises a wide spectrum of clinical manifestations.

Authors:  S Faghri; D Tamura; K H Kraemer; J J Digiovanna
Journal:  J Med Genet       Date:  2008-06-25       Impact factor: 6.318

4.  Persistence of repair proteins at unrepaired DNA damage distinguishes diseases with ERCC2 (XPD) mutations: cancer-prone xeroderma pigmentosum vs. non-cancer-prone trichothiodystrophy.

Authors:  Jennifer Boyle; Takahiro Ueda; Kyu-Seon Oh; Kyoko Imoto; Deborah Tamura; Jared Jagdeo; Sikandar G Khan; Carine Nadem; John J Digiovanna; Kenneth H Kraemer
Journal:  Hum Mutat       Date:  2008-10       Impact factor: 4.878

5.  Molecular and biochemical characterization of xrs mutants defective in Ku80.

Authors:  B K Singleton; A Priestley; H Steingrimsdottir; D Gell; T Blunt; S P Jackson; A R Lehmann; P A Jeggo
Journal:  Mol Cell Biol       Date:  1997-03       Impact factor: 4.272

6.  Mutations in the consensus helicase domains of the Werner syndrome gene. Werner's Syndrome Collaborative Group.

Authors:  C E Yu; J Oshima; E M Wijsman; J Nakura; T Miki; C Piussan; S Matthews; Y H Fu; J Mulligan; G M Martin; G D Schellenberg
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

7.  A mutation in the XPB/ERCC3 DNA repair transcription gene, associated with trichothiodystrophy.

Authors:  G Weeda; E Eveno; I Donker; W Vermeulen; O Chevallier-Lagente; A Taïeb; A Stary; J H Hoeijmakers; M Mezzina; A Sarasin
Journal:  Am J Hum Genet       Date:  1997-02       Impact factor: 11.025

8.  Adverse effects of trichothiodystrophy DNA repair and transcription gene disorder on human fetal development.

Authors:  R Moslehi; C Signore; D Tamura; J L Mills; J J Digiovanna; M A Tucker; J Troendle; T Ueda; J Boyle; S G Khan; K-S Oh; A M Goldstein; K H Kraemer
Journal:  Clin Genet       Date:  2009-12-10       Impact factor: 4.438

9.  The human CSB (ERCC6) gene corrects the transcription-coupled repair defect in the CHO cell mutant UV61.

Authors:  D K Orren; G L Dianov; V A Bohr
Journal:  Nucleic Acids Res       Date:  1996-09-01       Impact factor: 16.971

10.  Differentiation driven changes in the dynamic organization of Basal transcription initiation.

Authors:  Giuseppina Giglia-Mari; Arjan F Theil; Pierre-Olivier Mari; Sophie Mourgues; Julie Nonnekens; Lise O Andrieux; Jan de Wit; Catherine Miquel; Nils Wijgers; Alex Maas; Maria Fousteri; Jan H J Hoeijmakers; Wim Vermeulen
Journal:  PLoS Biol       Date:  2009-10-20       Impact factor: 8.029

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