4.3 Review

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

Journal

DNA REPAIR
Volume 9, Issue 3, Pages 325-330

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.dnarep.2010.01.006

Keywords

RECQ protein; Rothmund-Thomson syndrome; Baller-Gerold syndrome

Funding

  1. NIH
  2. Breast Cancer Alliance

Ask authors/readers for more resources

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.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.3
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available