Literature DB >> 16925525

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

Sudha Sharma1, Kevin M Doherty, Robert M Brosh.   

Abstract

Helicases are molecular motor proteins that couple the hydrolysis of NTP to nucleic acid unwinding. The growing number of DNA helicases implicated in human disease suggests that their vital specialized roles in cellular pathways are important for the maintenance of genome stability. In particular, mutations in genes of the RecQ family of DNA helicases result in chromosomal instability diseases of premature aging and/or cancer predisposition. We will discuss the mechanisms of RecQ helicases in pathways of DNA metabolism. A review of RecQ helicases from bacteria to human reveals their importance in genomic stability by their participation with other proteins to resolve DNA replication and recombination intermediates. In the light of their known catalytic activities and protein interactions, proposed models for RecQ function will be summarized with an emphasis on how this distinct class of enzymes functions in chromosomal stability maintenance and prevention of human disease and cancer.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16925525      PMCID: PMC1559444          DOI: 10.1042/BJ20060450

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  284 in total

Review 1.  G-quadruplex DNA: a potential target for anti-cancer drug design.

Authors:  H Han; L H Hurley
Journal:  Trends Pharmacol Sci       Date:  2000-04       Impact factor: 14.819

2.  Ku complex interacts with and stimulates the Werner protein.

Authors:  M P Cooper; A Machwe; D K Orren; R M Brosh; D Ramsden; V A Bohr
Journal:  Genes Dev       Date:  2000-04-15       Impact factor: 11.361

3.  The three-dimensional structure of the HRDC domain and implications for the Werner and Bloom syndrome proteins.

Authors:  Z Liu; M J Macias; M J Bottomley; G Stier; J P Linge; M Nilges; P Bork; M Sattler
Journal:  Structure       Date:  1999-12-15       Impact factor: 5.006

4.  Telomerase prevents the accelerated cell ageing of Werner syndrome fibroblasts.

Authors:  F S Wyllie; C J Jones; J W Skinner; M F Haughton; C Wallis; D Wynford-Thomas; R G Faragher; D Kipling
Journal:  Nat Genet       Date:  2000-01       Impact factor: 38.330

5.  The Bloom's syndrome gene product interacts with topoisomerase III.

Authors:  L Wu; S L Davies; P S North; H Goulaouic; J F Riou; H Turley; K C Gatter; I D Hickson
Journal:  J Biol Chem       Date:  2000-03-31       Impact factor: 5.157

6.  Human RecQ5beta, a large isomer of RecQ5 DNA helicase, localizes in the nucleoplasm and interacts with topoisomerases 3alpha and 3beta.

Authors:  A Shimamoto; K Nishikawa; S Kitao; Y Furuichi
Journal:  Nucleic Acids Res       Date:  2000-04-01       Impact factor: 16.971

7.  Functional interaction between the Werner Syndrome protein and DNA polymerase delta.

Authors:  A S Kamath-Loeb; E Johansson; P M Burgers; L A Loeb
Journal:  Proc Natl Acad Sci U S A       Date:  2000-04-25       Impact factor: 11.205

8.  Association of the Bloom syndrome protein with topoisomerase IIIalpha in somatic and meiotic cells.

Authors:  F B Johnson; D B Lombard; N F Neff; M A Mastrangelo; W Dewolf; N A Ellis; R A Marciniak; Y Yin; R Jaenisch; L Guarente
Journal:  Cancer Res       Date:  2000-03-01       Impact factor: 12.701

9.  WRN helicase expression in Werner syndrome cell lines.

Authors:  M J Moser; A S Kamath-Loeb; J E Jacob; S E Bennett; J Oshima; R J Monnat
Journal:  Nucleic Acids Res       Date:  2000-01-15       Impact factor: 16.971

10.  The Werner syndrome gene product co-purifies with the DNA replication complex and interacts with PCNA and topoisomerase I.

Authors:  M Lebel; E A Spillare; C C Harris; P Leder
Journal:  J Biol Chem       Date:  1999-12-31       Impact factor: 5.157

View more
  103 in total

1.  Conserved helicase domain of human RecQ4 is required for strand annealing-independent DNA unwinding.

Authors:  Marie L Rossi; Avik K Ghosh; Tomasz Kulikowicz; Deborah L Croteau; Vilhelm A Bohr
Journal:  DNA Repair (Amst)       Date:  2010-05-06

Review 2.  RecQ helicases; at the crossroad of genome replication, repair, and recombination.

Authors:  Sarallah Rezazadeh
Journal:  Mol Biol Rep       Date:  2011-09-23       Impact factor: 2.316

3.  Delineation of WRN helicase function with EXO1 in the replicational stress response.

Authors:  Monika Aggarwal; Joshua A Sommers; Christa Morris; Robert M Brosh
Journal:  DNA Repair (Amst)       Date:  2010-05-05

4.  The adenovirus E1b55K/E4orf6 complex induces degradation of the Bloom helicase during infection.

Authors:  Nicole I Orazio; Colleen M Naeger; Jan Karlseder; Matthew D Weitzman
Journal:  J Virol       Date:  2010-12-01       Impact factor: 5.103

5.  RECQL5 has unique strand annealing properties relative to the other human RecQ helicase proteins.

Authors:  Prabhat Khadka; Deborah L Croteau; Vilhelm A Bohr
Journal:  DNA Repair (Amst)       Date:  2015-12-02

Review 6.  Developing master keys to brain pathology, cancer and aging from the structural biology of proteins controlling reactive oxygen species and DNA repair.

Authors:  J J P Perry; L Fan; J A Tainer
Journal:  Neuroscience       Date:  2006-12-15       Impact factor: 3.590

7.  Association of RECQL5 gene polymorphisms and osteosarcoma in a Chinese Han population.

Authors:  Li-Qiang Zhi; Wei Ma; Hong Zhang; Si-Xiang Zeng; Bo Chen
Journal:  Tumour Biol       Date:  2013-11-28

Review 8.  Genome stability roles of SUMO-targeted ubiquitin ligases.

Authors:  J Heideker; J J P Perry; M N Boddy
Journal:  DNA Repair (Amst)       Date:  2009-02-23

9.  Haplotype analysis of RECQL5 gene and laryngeal cancer.

Authors:  Ying Qi; Xu Zhou
Journal:  Tumour Biol       Date:  2013-11-09

Review 10.  FANCJ helicase operates in the Fanconi Anemia DNA repair pathway and the response to replicational stress.

Authors:  Yuliang Wu; Robert M Brosh
Journal:  Curr Mol Med       Date:  2009-05       Impact factor: 2.222

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.