Roles of the Bloom's syndrome helicase in the maintenance of genome stability

Cheok, C. F., Bachrati, Csanad, Chan, K. L., Ralf, C., Wu, L. and Hickson, I. D. (2005) Roles of the Bloom's syndrome helicase in the maintenance of genome stability. Biochemical Society Transactions, 33 (6). pp. 1456-1459. ISSN 0300-5127

Full content URL: http://dx.doi.org/10.1042/BST20051456

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Abstract

The RecQ family of DNA helicases is highly conserved in evolution from bacteria to humans. Of the five known human RecQ family members, three (BLM, WRN and RECQ4, which cause Bloom's syndrome, Werner's syndrome and Rothmund-Thomson syndrome respectively) are mutated in distinct clinical disorders associated with cancer predisposition and/or premature aging. BLM forms part of a multienzyme complex including topoisomerase IIIalpha, replication protein A and a newly identified factor called BLAP75. Together, these proteins play a role in the resolution of DNA structures that arise during the process of homologous recombination repair. In the absence of BLM, cells show genomic instability and a high incidence of sister-chromatid exchanges. In addition to a DNA structure-specific helicase activity, BLM also catalyses Holliday-junction branch migration and the annealing of complementary single-stranded DNA molecules.

Keywords:Bloom syndrome, BLM, RecQ helicases
Subjects:C Biological Sciences > C700 Molecular Biology, Biophysics and Biochemistry
Divisions:College of Science > School of Life Sciences
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ID Code:8888
Deposited On:17 Apr 2013 07:57

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