Literature DB >> 19942596

Newly identified CHO ERCC3/XPB mutations and phenotype characterization.

Ivana Rybanská1, Ján Gursky, Miriam Fasková, Edmund P Salazar, Erika Kimlícková-Polakovicová, Karol Kleibl, Larry H Thompson, Miroslav Pirsel.   

Abstract

Nucleotide excision repair (NER) is a complex multistage process involving many interacting gene products to repair a wide range of DNA lesions. Genetic defects in NER cause human hereditary diseases including xeroderma pigmentosum (XP), Cockayne syndrome (CS), trichothiodystrophy and a combined XP/CS overlapping symptom. One key gene product associated with all these disorders is the excision repair cross-complementing 3/xeroderma pigmentosum B (ERCC3/XPB) DNA helicase, a subunit of the transcription factor IIH complex. ERCC3 is involved in initiation of basal transcription and global genome repair as well as in transcription-coupled repair (TCR). The hamster ERCC3 gene shows high degree of homology with the human ERCC3/XPB gene. We identified new mutations in the Chinese hamster ovary cell ERCC3 gene and characterized the role of hamster ERCC3 protein in DNA repair of ultraviolet (UV)-induced and oxidative DNA damage. All but one newly described mutations are located in the protein C-terminal region around the last intron-exon boundary. Due to protein truncations or frameshifts, they lack amino acid Ser751, phosphorylation of which prevents the 5' incision of the UV-induced lesion during NER. Thus, despite the various locations of the mutations, their phenotypes are similar. All ercc3 mutants are extremely sensitive to UV-C light and lack recovery of RNA synthesis (RRS), confirming a defect in TCR of UV-induced damage. Their limited global genome NER capacity averages approximately 8%. We detected modest sensitivity of ercc3 mutants to the photosensitizer Ro19-8022, which primarily introduces 8-oxoguanine lesions into DNA. Ro19-8022-induced damage interfered with RRS, and some of the ercc3 mutants had delayed kinetics. All ercc3 mutants showed efficient base excision repair (BER). Thus, the positions of the mutations have no effect on the sensitivity to, and repair of, Ro19-8022-induced DNA damage, suggesting that the ERCC3 protein is not involved in BER.

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Year:  2009        PMID: 19942596      PMCID: PMC2825344          DOI: 10.1093/mutage/gep059

Source DB:  PubMed          Journal:  Mutagenesis        ISSN: 0267-8357            Impact factor:   3.000


  55 in total

Review 1.  Helicase motifs: the engine that powers DNA unwinding.

Authors:  M C Hall; S W Matson
Journal:  Mol Microbiol       Date:  1999-12       Impact factor: 3.501

2.  Phenotypic heterogeneity in the XPB DNA helicase gene (ERCC3): xeroderma pigmentosum without and with Cockayne syndrome.

Authors:  Kyu-Seon Oh; Sikandar G Khan; N G J Jaspers; Anja Raams; Takahiro Ueda; Alan Lehmann; Peter S Friedmann; Steffen Emmert; Alexi Gratchev; Katherine Lachlan; Anneke Lucassan; Carl C Baker; Kenneth H Kraemer
Journal:  Hum Mutat       Date:  2006-11       Impact factor: 4.878

3.  RNA polymerase II bypass of oxidative DNA damage is regulated by transcription elongation factors.

Authors:  Nicolas Charlet-Berguerand; Sascha Feuerhahn; Stephanie E Kong; Howard Ziserman; Joan W Conaway; Ronald Conaway; Jean Marc Egly
Journal:  EMBO J       Date:  2006-11-16       Impact factor: 11.598

Review 4.  DNA repair in mammalian cells : Nucleotide excision repair: variations on versatility.

Authors:  T Nouspikel
Journal:  Cell Mol Life Sci       Date:  2009-03       Impact factor: 9.261

Review 5.  Xeroderma pigmentosum, trichothiodystrophy and Cockayne syndrome: a complex genotype-phenotype relationship.

Authors:  K H Kraemer; N J Patronas; R Schiffmann; B P Brooks; D Tamura; J J DiGiovanna
Journal:  Neuroscience       Date:  2007-02-01       Impact factor: 3.590

6.  Transcription coupled repair of 8-oxoguanine in murine cells: the ogg1 protein is required for repair in nontranscribed sequences but not in transcribed sequences.

Authors:  F Le Page; A Klungland; D E Barnes; A Sarasin; S Boiteux
Journal:  Proc Natl Acad Sci U S A       Date:  2000-07-18       Impact factor: 11.205

7.  Distinct roles for the XPB/p52 and XPD/p44 subcomplexes of TFIIH in damaged DNA opening during nucleotide excision repair.

Authors:  Frédéric Coin; Valentyn Oksenych; Jean-Marc Egly
Journal:  Mol Cell       Date:  2007-04-27       Impact factor: 17.970

8.  An Xpb mouse model for combined xeroderma pigmentosum and cockayne syndrome reveals progeroid features upon further attenuation of DNA repair.

Authors:  Jaan-Olle Andressoo; Geert Weeda; Jan de Wit; James R Mitchell; Rudolf B Beems; Harry van Steeg; Gijsbertus T J van der Horst; Jan H Hoeijmakers
Journal:  Mol Cell Biol       Date:  2008-12-29       Impact factor: 4.272

Review 9.  DNA repair in mammalian cells: Transcription-coupled DNA repair: directing your effort where it's most needed.

Authors:  S Tornaletti
Journal:  Cell Mol Life Sci       Date:  2009-03       Impact factor: 9.261

Review 10.  Bulky DNA lesions induced by reactive oxygen species.

Authors:  Yinsheng Wang
Journal:  Chem Res Toxicol       Date:  2008-01-12       Impact factor: 3.739

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  4 in total

1.  piRNA profiling during specific stages of mouse spermatogenesis.

Authors:  Haiyun Gan; Xiwen Lin; Zhuqiang Zhang; Wei Zhang; Shangying Liao; Lixian Wang; Chunsheng Han
Journal:  RNA       Date:  2011-05-20       Impact factor: 4.942

2.  A population-based study of DNA repair gene variants in relation to non-melanoma skin cancer as a marker of a cancer-prone phenotype.

Authors:  Ingo Ruczinski; Timothy J Jorgensen; Yin Yao Shugart; Yvette Berthier Schaad; Bailey Kessing; Judith Hoffman-Bolton; Kathy J Helzlsouer; W H Linda Kao; Lee Wheless; Lesley Francis; Rhoda M Alani; Paul T Strickland; Michael W Smith; Anthony J Alberg
Journal:  Carcinogenesis       Date:  2012-05-11       Impact factor: 4.944

3.  Hydrogen peroxide induced genomic instability in nucleotide excision repair-deficient lymphoblastoid cells.

Authors:  Kalpana Gopalakrishnan; Grace Kah Mun Low; Aloysius Poh Leong Ting; Prarthana Srikanth; Predrag Slijepcevic; M Prakash Hande
Journal:  Genome Integr       Date:  2010-12-22

4.  Identification of genes involved in low aminoglycoside-induced SOS response in Vibrio cholerae: a role for transcription stalling and Mfd helicase.

Authors:  Zeynep Baharoglu; Anamaria Babosan; Didier Mazel
Journal:  Nucleic Acids Res       Date:  2013-12-06       Impact factor: 16.971

  4 in total

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