Literature DB >> 14726023

Human diseases deficient in RecQ helicases.

J A Harrigan1, V A Bohr.   

Abstract

RecQ helicases are conserved from bacteria to man. Mutations in three of the human RecQ family members give rise to genetic disorders characterized by genomic instability and a predisposition to cancer. RecQ helicases are therefore caretakers of the genome, and although they do not directly regulate tumorigenesis, they influence stability and the rate of accumulation of genetic alterations, which in turn, result in tumorigenesis. Maintenance of genome stability by RecQ helicases likely involves their participation in DNA replication, recombination, and repair pathways.

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Year:  2003        PMID: 14726023     DOI: 10.1016/j.biochi.2003.10.006

Source DB:  PubMed          Journal:  Biochimie        ISSN: 0300-9084            Impact factor:   4.079


  16 in total

1.  RecQ helicase translocates along single-stranded DNA with a moderate processivity and tight mechanochemical coupling.

Authors:  Kata Sarlós; Máté Gyimesi; Mihály Kovács
Journal:  Proc Natl Acad Sci U S A       Date:  2012-06-04       Impact factor: 11.205

Review 2.  Genetic and epigenetic features in radiation sensitivity. Part II: implications for clinical practice and radiation protection.

Authors:  Michel H Bourguignon; Pablo A Gisone; Maria R Perez; Severino Michelin; Diana Dubner; Marina Di Giorgio; Edgardo D Carosella
Journal:  Eur J Nucl Med Mol Imaging       Date:  2005-03       Impact factor: 9.236

Review 3.  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

4.  A helical bundle in the N-terminal domain of the BLM helicase mediates dimer and potentially hexamer formation.

Authors:  Jing Shi; Wei-Fei Chen; Bo Zhang; San-Hong Fan; Xia Ai; Na-Nv Liu; Stephane Rety; Xu-Guang Xi
Journal:  J Biol Chem       Date:  2017-02-22       Impact factor: 5.157

5.  [Hereditary bone tumors].

Authors:  D Baumhoer
Journal:  Pathologe       Date:  2017-05       Impact factor: 1.011

6.  A nucleotide-dependent and HRDC domain-dependent structural transition in DNA-bound RecQ helicase.

Authors:  Zsuzsa S Kocsis; Kata Sarlós; Gábor M Harami; Máté Martina; Mihály Kovács
Journal:  J Biol Chem       Date:  2014-01-08       Impact factor: 5.157

7.  [Hereditary bone tumors].

Authors:  G Jundt; D Baumhoer
Journal:  Pathologe       Date:  2010-10       Impact factor: 1.011

Review 8.  DNA repair deficiency and neurological disease.

Authors:  Peter J McKinnon
Journal:  Nat Rev Neurosci       Date:  2009-01-15       Impact factor: 34.870

9.  Poly(ADP-ribose) polymerase 1 regulates both the exonuclease and helicase activities of the Werner syndrome protein.

Authors:  Cayetano von Kobbe; Jeanine A Harrigan; Valérie Schreiber; Patrick Stiegler; Jason Piotrowski; Lale Dawut; Vilhelm A Bohr
Journal:  Nucleic Acids Res       Date:  2004-08-03       Impact factor: 16.971

10.  RECQ1 possesses DNA branch migration activity.

Authors:  Dmitry V Bugreev; Robert M Brosh; Alexander V Mazin
Journal:  J Biol Chem       Date:  2008-05-21       Impact factor: 5.157

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