Literature DB >> 20096650

Rothmund-Thomson syndrome helicase, RECQ4: on the crossroad between DNA replication and repair.

Yilun Liu1.   

Abstract

RECQ proteins are conserved DNA helicases in both prokaryotes and eukaryotes. The importance of the RECQ family helicases in human health is demonstrated by their roles as cancer suppressors that are vital for preserving genome integrity. Mutations in one of the RECQ family proteins, RECQ4, not only result in developmental abnormalities and cancer predispositions, but are also linked to premature aging. Therefore, defining the function and regulation of the RECQ4 protein is fundamental to our understanding of both the aging process and cancer pathogenesis. This review will summarize the clinical effect of RECQ4 in human health, and discuss the recent progress and debate in defining the complex molecular function of RECQ4 in DNA metabolism. (c) 2010 Elsevier B.V. All rights reserved.

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Year:  2010        PMID: 20096650     DOI: 10.1016/j.dnarep.2010.01.006

Source DB:  PubMed          Journal:  DNA Repair (Amst)        ISSN: 1568-7856


  19 in total

1.  RecQL4 cytoplasmic localization: implications in mitochondrial DNA oxidative damage repair.

Authors:  Zhenfen Chi; Linghu Nie; Zhao Peng; Qiong Yang; Kuan Yang; Jiahai Tao; Yang Mi; Xiangdong Fang; Adayabalam S Balajee; Yongliang Zhao
Journal:  Int J Biochem Cell Biol       Date:  2012-07-21       Impact factor: 5.085

2.  Hrq1, a homolog of the human RecQ4 helicase, acts catalytically and structurally to promote genome integrity.

Authors:  Matthew L Bochman; Katrin Paeschke; Angela Chan; Virginia A Zakian
Journal:  Cell Rep       Date:  2014-01-16       Impact factor: 9.423

3.  RECQL4, the protein mutated in Rothmund-Thomson syndrome, functions in telomere maintenance.

Authors:  Avik K Ghosh; Marie L Rossi; Dharmendra Kumar Singh; Christopher Dunn; Mahesh Ramamoorthy; Deborah L Croteau; Yie Liu; Vilhelm A Bohr
Journal:  J Biol Chem       Date:  2011-10-28       Impact factor: 5.157

Review 4.  Helicase-inactivating mutations as a basis for dominant negative phenotypes.

Authors:  Yuliang Wu; Robert M Brosh
Journal:  Cell Cycle       Date:  2010-10-15       Impact factor: 4.534

Review 5.  Human RECQ helicases: roles in DNA metabolism, mutagenesis and cancer biology.

Authors:  Raymond J Monnat
Journal:  Semin Cancer Biol       Date:  2010-10-08       Impact factor: 15.707

6.  Activation of p38 MAP kinase and stress signalling in fibroblasts from the progeroid Rothmund-Thomson syndrome.

Authors:  Terence Davis; Hannah S E Tivey; Amy J C Brook; Julia W Grimstead; Michal J Rokicki; David Kipling
Journal:  Age (Dordr)       Date:  2012-09-22

7.  Impaired p32 regulation caused by the lymphoma-prone RECQ4 mutation drives mitochondrial dysfunction.

Authors:  Jiin-Tarng Wang; Xiaohua Xu; Aileen Y Alontaga; Yuan Chen; Yilun Liu
Journal:  Cell Rep       Date:  2014-04-17       Impact factor: 9.423

Review 8.  Evolutionary conservation of the CDK targets in eukaryotic DNA replication initiation.

Authors:  Philip Zegerman
Journal:  Chromosoma       Date:  2015-01-11       Impact factor: 4.316

9.  Human HEL308 localizes to damaged replication forks and unwinds lagging strand structures.

Authors:  Agnieszka A Tafel; Leonard Wu; Peter J McHugh
Journal:  J Biol Chem       Date:  2011-03-11       Impact factor: 5.157

Review 10.  Borrowing nuclear DNA helicases to protect mitochondrial DNA.

Authors:  Lin Ding; Yilun Liu
Journal:  Int J Mol Sci       Date:  2015-05-13       Impact factor: 5.923

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