Literature DB >> 11316787

Loss of Werner syndrome protein function promotes aberrant mitotic recombination.

P R Prince1, M J Emond, R J Monnat.   

Abstract

The chromosome 8p11-12 Werner syndrome (WRN ) locus encodes a RecQ helicase protein of unknown function that possesses both 3' --> 5' helicase and 3' --> 5' exonuclease activities. We show that WRN cell lines display a marked reduction in cell proliferation following mitotic recombination, and generate few viable gene conversion-type recombinants. These findings indicate that WRN plays a role in mitotic recombination, and that a loss of WRN function may promote genetic instability and disease via recombination-initiated mitotic arrest, cell death, or gene rearrangement.

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Year:  2001        PMID: 11316787      PMCID: PMC312674          DOI: 10.1101/gad.877001

Source DB:  PubMed          Journal:  Genes Dev        ISSN: 0890-9369            Impact factor:   11.361


  41 in total

1.  Werner's syndrome protein (WRN) migrates Holliday junctions and co-localizes with RPA upon replication arrest.

Authors:  A Constantinou; M Tarsounas; J K Karow; R M Brosh; V A Bohr; I D Hickson; S C West
Journal:  EMBO Rep       Date:  2000-07       Impact factor: 8.807

2.  Homologous recombination is responsible for cell death in the absence of the Sgs1 and Srs2 helicases.

Authors:  S Gangloff; C Soustelle; F Fabre
Journal:  Nat Genet       Date:  2000-06       Impact factor: 38.330

3.  Immortalization of Werner syndrome and progeria fibroblasts.

Authors:  H Saito; R E Moses
Journal:  Exp Cell Res       Date:  1991-02       Impact factor: 3.905

4.  Branch migration and Holliday junction resolution catalyzed by activities from mammalian cells.

Authors:  A Constantinou; A A Davies; S C West
Journal:  Cell       Date:  2001-01-26       Impact factor: 41.582

5.  Detection of transcribable recombination products following conjugation in rec+, reCB- and recC-strains of Escherichia coli K12.

Authors:  E A Birge; K B Low
Journal:  J Mol Biol       Date:  1974-03-15       Impact factor: 5.469

6.  Estimation of mutation rates in cultured mammalian cells.

Authors:  I C Li; J Fu; Y T Hung; E H Chu
Journal:  Mutat Res       Date:  1983-10       Impact factor: 2.433

Review 7.  The Werner syndrome gene: the molecular basis of RecQ helicase-deficiency diseases.

Authors:  J C Shen; L A Loeb
Journal:  Trends Genet       Date:  2000-05       Impact factor: 11.639

Review 8.  DNA double strand break repair in mammalian cells.

Authors:  P Karran
Journal:  Curr Opin Genet Dev       Date:  2000-04       Impact factor: 5.578

9.  Nucleolar localization of the Werner syndrome protein in human cells.

Authors:  R A Marciniak; D B Lombard; F B Johnson; L Guarente
Journal:  Proc Natl Acad Sci U S A       Date:  1998-06-09       Impact factor: 11.205

10.  Mutator phenotype of Werner syndrome is characterized by extensive deletions.

Authors:  K Fukuchi; G M Martin; R J Monnat
Journal:  Proc Natl Acad Sci U S A       Date:  1989-08       Impact factor: 11.205

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  58 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

Review 2.  Mechanisms of RecQ helicases in pathways of DNA metabolism and maintenance of genomic stability.

Authors:  Sudha Sharma; Kevin M Doherty; Robert M Brosh
Journal:  Biochem J       Date:  2006-09-15       Impact factor: 3.857

3.  Non-B DNA-forming sequences and WRN deficiency independently increase the frequency of base substitution in human cells.

Authors:  Albino Bacolla; Guliang Wang; Aklank Jain; Nadia A Chuzhanova; Regina Z Cer; Jack R Collins; David N Cooper; Vilhelm A Bohr; Karen M Vasquez
Journal:  J Biol Chem       Date:  2011-02-01       Impact factor: 5.157

4.  Hyperinsulinemia and insulin resistance in Wrn null mice fed a diabetogenic diet.

Authors:  Gina Moore; Susan Knoblaugh; Kathryn Gollahon; Peter Rabinovitch; Warren Ladiges
Journal:  Mech Ageing Dev       Date:  2008-01-17       Impact factor: 5.432

5.  Tissue-specific differences in the accumulation of sequence rearrangements with age.

Authors:  Dominika M Wiktor-Brown; Werner Olipitz; Carrie A Hendricks; Rebecca E Rugo; Bevin P Engelward
Journal:  DNA Repair (Amst)       Date:  2008-03-20

6.  Werner syndrome protein interacts functionally with translesion DNA polymerases.

Authors:  Ashwini S Kamath-Loeb; Li Lan; Satoshi Nakajima; Akira Yasui; Lawrence A Loeb
Journal:  Proc Natl Acad Sci U S A       Date:  2007-06-11       Impact factor: 11.205

7.  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

8.  Werner syndrome protein limits MYC-induced cellular senescence.

Authors:  Carla Grandori; Kou-Juey Wu; Paula Fernandez; Celine Ngouenet; Jonathan Grim; Bruce E Clurman; Michael J Moser; Junko Oshima; David W Russell; Karen Swisshelm; Scott Frank; Bruno Amati; Riccardo Dalla-Favera; Raymond J Monnat
Journal:  Genes Dev       Date:  2003-07-01       Impact factor: 11.361

9.  WRN helicase and FEN-1 form a complex upon replication arrest and together process branchmigrating DNA structures associated with the replication fork.

Authors:  Sudha Sharma; Marit Otterlei; Joshua A Sommers; Henry C Driscoll; Grigory L Dianov; Hui-I Kao; Robert A Bambara; Robert M Brosh
Journal:  Mol Biol Cell       Date:  2003-12-02       Impact factor: 4.138

10.  The Werner syndrome helicase/exonuclease processes mobile D-loops through branch migration and degradation.

Authors:  Patricia L Opresko; Gregory Sowd; Hong Wang
Journal:  PLoS One       Date:  2009-03-13       Impact factor: 3.240

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