Literature DB >> 8976161

Werner syndrome: entering the helicase era.

C J Epstein1, A G Motulsky.   

Abstract

Werner syndrome is a rare autosomal recessive disorder that mimics some of the characteristics of aging. The gene for this disorder has recently been identified as a helicase of the recQ subclass. Other phenotypically distinctive disorders caused by different helicase mutations include Bloom syndrome, Cockayne syndrome, xeroderma pigmentosum and trichothiodystrophy. Possible mechanisms by which helicases might produce the variable phenotypes are discussed. These include altered nucleotide excision repair and RNA polymerase II-mediated transcription. The discovery of the helicase defect in Werner syndrome provides a road map for future study of its unique pathogenesis and conceivable, but unproved, relationship to the aging process.

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Year:  1996        PMID: 8976161     DOI: 10.1002/bies.950181214

Source DB:  PubMed          Journal:  Bioessays        ISSN: 0265-9247            Impact factor:   4.345


  10 in total

1.  Analyses of the interaction between the origin binding domain from simian virus 40 T antigen and single-stranded DNA provide insights into DNA unwinding and initiation of DNA replication.

Authors:  Danielle K Reese; Gretchen Meinke; Anuradha Kumar; Stephanie Moine; Kathleen Chen; James L Sudmeier; William Bachovchin; Andrew Bohm; Peter A Bullock
Journal:  J Virol       Date:  2006-09-27       Impact factor: 5.103

Review 2.  Progeroid syndromes: probing the molecular basis of aging?

Authors:  D Kipling; R G Faragher
Journal:  Mol Pathol       Date:  1997-10

3.  Werner protein protects nonproliferating cells from oxidative DNA damage.

Authors:  Anna M Szekely; Franziska Bleichert; Astrid Nümann; Stephen Van Komen; Elisabeth Manasanch; Abdelhakim Ben Nasr; Allon Canaan; Sherman M Weissman
Journal:  Mol Cell Biol       Date:  2005-12       Impact factor: 4.272

4.  A DNA helicase purified by replication protein A (RPA) affinity chromatography from mouse FM3A cells.

Authors:  P Hughes; G Baldacci
Journal:  Nucleic Acids Res       Date:  1997-10-01       Impact factor: 16.971

5.  Comparative sequence analysis of ribonucleases HII, III, II PH and D.

Authors:  I S Mian
Journal:  Nucleic Acids Res       Date:  1997-08-15       Impact factor: 16.971

6.  The N-terminal region of the Schizosaccharomyces pombe RecQ helicase, Rqh1p, physically interacts with Topoisomerase III and is required for Rqh1p function.

Authors:  Fouzia Ahmad; Elspeth Stewart
Journal:  Mol Genet Genomics       Date:  2005-02-09       Impact factor: 3.291

7.  Age-associated decreases in human DNA repair capacity: Implications for the skin.

Authors:  I M Hadshiew; M S Eller; B A Gilchrest
Journal:  Age (Omaha)       Date:  1999-04

8.  Requirement of Rrm3 helicase for repair of spontaneous DNA lesions in cells lacking Srs2 or Sgs1 helicase.

Authors:  Kristina H Schmidt; Richard D Kolodner
Journal:  Mol Cell Biol       Date:  2004-04       Impact factor: 4.272

Review 9.  Werner Syndrome Protein and DNA Replication.

Authors:  Shibani Mukherjee; Debapriya Sinha; Souparno Bhattacharya; Kalayarasan Srinivasan; Salim Abdisalaam; Aroumougame Asaithamby
Journal:  Int J Mol Sci       Date:  2018-11-02       Impact factor: 5.923

Review 10.  MUT-7 Provides Molecular Insight into the Werner Syndrome Exonuclease.

Authors:  Tsung-Yuan Hsu; Ling-Nung Hsu; Shih-Yu Chen; Bi-Tzen Juang
Journal:  Cells       Date:  2021-12-08       Impact factor: 6.600

  10 in total

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