WRN exonuclease structure and molecular mechanism imply an editing role in DNA end processing-Reference-Cited by-同舟云学术

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WRN exonuclease structure and molecular mechanism imply an editing role in DNA end processing

Published:2006-04-23 Issue:5 Volume:13 Page:414-422
ISSN:1545-9993
Container-title:Nature Structural & Molecular Biology
language:en
Short-container-title:Nat Struct Mol Biol

Author:

Perry J Jefferson P,Yannone Steven M,Holden Lauren G,Hitomi Chiharu,Asaithamby Aroumougame,Han Seungil,Cooper Priscilla K,Chen David J,Tainer John A

Publisher

Springer Science and Business Media LLC

Subject

Molecular Biology,Structural Biology

Link

http://www.nature.com/articles/nsmb1088.pdf

Reference50 articles.

1. Goto, M. Hierarchical deterioration of body systems in Werner's syndrome: implications for normal ageing. Mech. Ageing Dev. 98, 239–254 (1997).

2. Opresko, P.L., Cheng, W.H., von Kobbe, C., Harrigan, J.A. & Bohr, V.A. Werner syndrome and the function of the Werner protein; what they can teach us about the molecular aging process. Carcinogenesis 24, 791–802 (2003).

3. Yu, C.E. et al. Positional cloning of the Werner's syndrome gene. Science 272, 258–262 (1996).

4. von Kobbe, C. & Bohr, V.A. A nucleolar targeting sequence in the Werner syndrome protein resides within residues 949–1092. J. Cell Sci. 115, 3901–3907 (2002).

5. Matsumoto, T., Shimamoto, A., Goto, M. & Furuichi, Y. Impaired nuclear localization of defective DNA helicases in Werner's syndrome. Nat. Genet. 16, 335–336 (1997).

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