Literature DB >> 10480367

Cell fusion corrects the 4-nitroquinoline 1-oxide sensitivity of Werner syndrome fibroblast cell lines.

P R Prince1, C E Ogburn, M J Moser, M J Emond, G M Martin, R J Monnat.   

Abstract

We have shown that Werner syndrome (WRN) fibroblast cell lines are unusually sensitive to the DNA-damaging agent 4-nitroquinoline 1-oxide (4NQO), though not to gamma radiation or to hydrogen peroxide. The fusion of 4NQO-sensitive WRN and 4NQO-resistant control fibroblast cell lines generated proliferating WRN x control cell hybrids that expressed WRN protein and were 4NQO-resistant. These results establish the recessive nature of 4NQO sensitivity in WRN cell lines and provide a cellular assay for WRN protein function.

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Year:  1999        PMID: 10480367     DOI: 10.1007/s004399900078

Source DB:  PubMed          Journal:  Hum Genet        ISSN: 0340-6717            Impact factor:   4.132


  14 in total

1.  Telomere instability in a human tumor cell line expressing a dominant-negative WRN protein.

Authors:  Yongli Bai; John P Murnane
Journal:  Hum Genet       Date:  2003-06-25       Impact factor: 4.132

2.  Selective blockage of the 3'-->5' exonuclease activity of WRN protein by certain oxidative modifications and bulky lesions in DNA.

Authors:  A Machwe; R Ganunis; V A Bohr; D K Orren
Journal:  Nucleic Acids Res       Date:  2000-07-15       Impact factor: 16.971

3.  Loss of Werner syndrome protein function promotes aberrant mitotic recombination.

Authors:  P R Prince; M J Emond; R J Monnat
Journal:  Genes Dev       Date:  2001-04-15       Impact factor: 11.361

Review 4.  Human RECQ helicases: roles in DNA metabolism, mutagenesis and cancer biology.

Authors:  Raymond J Monnat
Journal:  Semin Cancer Biol       Date:  2010-10-08       Impact factor: 15.707

5.  Identification of a coiled coil in werner syndrome protein that facilitates multimerization and promotes exonuclease processivity.

Authors:  J Jefferson P Perry; Aroumougame Asaithamby; Adam Barnebey; Foad Kiamanesch; David J Chen; Seungil Han; John A Tainer; Steven M Yannone
Journal:  J Biol Chem       Date:  2010-06-01       Impact factor: 5.157

6.  Homologous recombination resolution defect in werner syndrome.

Authors:  Yannick Saintigny; Kate Makienko; Cristina Swanson; Mary J Emond; Raymond J Monnat
Journal:  Mol Cell Biol       Date:  2002-10       Impact factor: 4.272

7.  The Werner's Syndrome protein collaborates with REV1 to promote replication fork progression on damaged DNA.

Authors:  Lara G Phillips; Julian E Sale
Journal:  DNA Repair (Amst)       Date:  2010-08-05

8.  Divergent cellular phenotypes of human and mouse cells lacking the Werner syndrome RecQ helicase.

Authors:  Kiranjit K Dhillon; Julia M Sidorova; Tina M Albertson; Judith B Anderson; Warren C Ladiges; Peter S Rabinovitch; Bradley D Preston; Raymond J Monnat
Journal:  DNA Repair (Amst)       Date:  2009-11-05

9.  Sensitivity of RECQL4-deficient fibroblasts from Rothmund-Thomson syndrome patients to genotoxic agents.

Authors:  Weidong Jin; Hao Liu; Yiqun Zhang; Subhendu K Otta; Sharon E Plon; Lisa L Wang
Journal:  Hum Genet       Date:  2008-05-27       Impact factor: 4.132

Review 10.  From old organisms to new molecules: integrative biology and therapeutic targets in accelerated human ageing.

Authors:  L S Cox; R G A Faragher
Journal:  Cell Mol Life Sci       Date:  2007-10       Impact factor: 9.261

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