Literature DB >> 9852201

Characterization of the nuclear localization signal in the DNA helicase involved in Werner's syndrome.

T Matsumoto1, O Imamura, M Goto, Y Furuichi.   

Abstract

The nuclear localization signal (NLS) of the DNA helicase involved in Werner's syndrome (WS) was studied. Previously, we noted that the C-terminal region of WS helicase contains the NLS. In this study, we generated in HeLa cells various chimeric proteins consisting of the N-terminal tagged with an enhanced green fluorescent protein and the C-terminal fragments of the WS helicase that were truncated either from N- or C-termini, and we examined the ability of fragments to transfer the fusion proteins to the nucleoplasm by fluorescence microscopy. A small C-proximal region containing 34 amino acid residues (residues 1369-1402) was found to contain full nuclear migration activities. Subsequent amino acid substitution experiments showed that a sequence of three positively charged amino acids (Lys1371-Arg1372-Arg1373) in this region are particularly important. Similar sequence has previously been defined as the nuclear localization signal of SV-40 large T antigen that also acts as a viral DNA helicase. Conservation of this motif was found in the C-terminal regions of the other RecQ type DNA helicases, including murine WS helicase, yeast sgs1 and rqh+1 and human Bloom syndrome DNA helicases.

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Year:  1998        PMID: 9852201     DOI: 10.3892/ijmm.1.1.71

Source DB:  PubMed          Journal:  Int J Mol Med        ISSN: 1107-3756            Impact factor:   4.101


  11 in total

1.  WRN mutations in Werner syndrome patients: genomic rearrangements, unusual intronic mutations and ethnic-specific alterations.

Authors:  Katrin Friedrich; Lin Lee; Dru F Leistritz; Gudrun Nürnberg; Bidisha Saha; Fuki M Hisama; Daniel K Eyman; Davor Lessel; Peter Nürnberg; Chumei Li; María J Garcia-F-Villalta; Carolien M Kets; Joerg Schmidtke; Vítor Tedim Cruz; Peter C Van den Akker; Joseph Boak; Dincy Peter; Goli Compoginis; Kivanc Cefle; Sukru Ozturk; Norberto López; Theda Wessel; Martin Poot; P F Ippel; Birgit Groff-Kellermann; Holger Hoehn; George M Martin; Christian Kubisch; Junko Oshima
Journal:  Hum Genet       Date:  2010-05-05       Impact factor: 4.132

2.  Polymorphisms in DNA repair genes and risk of non-Hodgkin lymphoma among women in Connecticut.

Authors:  Min Shen; Tongzhang Zheng; Qing Lan; Yawei Zhang; Shelia H Zahm; Sophia S Wang; Theodore R Holford; Brian Leaderer; Meredith Yeager; Robert Welch; Daehee Kang; Peter Boyle; Bing Zhang; Kaiyong Zou; Yong Zhu; Stephen Chanock; Nathaniel Rothman
Journal:  Hum Genet       Date:  2006-04-26       Impact factor: 4.132

3.  High-resolution structure of the E.coli RecQ helicase catalytic core.

Authors:  Douglas A Bernstein; Morgan C Zittel; James L Keck
Journal:  EMBO J       Date:  2003-10-01       Impact factor: 11.598

4.  Polymorphisms of the WRN gene and DNA damage of peripheral lymphocytes in age-related cataract in a Han Chinese population.

Authors:  Shengqun Jiang; Nan Hu; Jing Zhou; Junfang Zhang; Ruifang Gao; Jianyan Hu; Huaijin Guan
Journal:  Age (Dordr)       Date:  2013-01-20

5.  Detection by epitope-defined monoclonal antibodies of Werner DNA helicases in the nucleoplasm and their upregulation by cell transformation and immortalization.

Authors:  M Shiratori; S Sakamoto; N Suzuki; Y Tokutake; Y Kawabe; T Enomoto; M Sugimoto; M Goto; T Matsumoto; Y Furuichi
Journal:  J Cell Biol       Date:  1999-01-11       Impact factor: 10.539

6.  Werner Syndrome.

Authors:  Lishan Chen; Junko Oshima
Journal:  J Biomed Biotechnol       Date:  2002

Review 7.  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

8.  A Novel WRN Frameshift Mutation Identified by Multiplex Genetic Testing in a Family with Multiple Cases of Cancer.

Authors:  Liu Yang; Guosheng Wang; Xinyi Zhao; Song Ye; Peng Shen; Weilin Wang; Shusen Zheng
Journal:  PLoS One       Date:  2015-08-04       Impact factor: 3.240

9.  Ethnic-Specific WRN Mutations in South Asian Werner Syndrome Patients: Potential Founder Effect in Patients with Indian or Pakistani Ancestry.

Authors:  Bidisha Saha; Davor Lessel; Sheela Nampoothiri; Anuradha S Rao; Fuki M Hisama; Dincy Peter; Chris Bennett; Gudrun Nürnberg; Peter Nürnberg; George M Martin; Christian Kubisch; Junko Oshima
Journal:  Mol Genet Genomic Med       Date:  2013-05-01       Impact factor: 2.183

10.  Catalytic activities of Werner protein are affected by adduction with 4-hydroxy-2-nonenal.

Authors:  Jolanta Czerwińska; Jarosław Poznański; Janusz Dębski; Zuzanna Bukowy; Vilhelm A Bohr; Barbara Tudek; Elżbieta Speina
Journal:  Nucleic Acids Res       Date:  2014-08-28       Impact factor: 16.971

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