Acetylation of Werner syndrome protein (WRN): relationships with DNA damage, DNA replication and DNA metabolic activities
Author:
Publisher
Springer Science and Business Media LLC
Subject
Geriatrics and Gerontology,Gerontology,Aging
Link
http://link.springer.com/content/pdf/10.1007/s10522-014-9506-3.pdf
Reference84 articles.
1. Blander G, Zalle N, Daniely Y, Taplick J, Gray MD, Oren M (2002) DNA damage-induced translocation of the Werner helicase is regulated by acetylation. J Biol Chem 277:50934–50940
2. Brosh RM Jr, Orren DK, Nehlin JO, Ravn PH, Kenny MK, Machwe A, Bohr VA (1999) Functional and physical interaction between WRN helicase and human replication protein A. J Biol Chem 274:18341–18350
3. Brosh RM Jr, Majumdar A, Desai S, Hickson ID, Bohr VA, Seidman MM (2001a) Unwinding of a DNA triple helix by the Werner and Bloom syndrome helicases. J Biol Chem 276:3024–3030
4. Brosh RM Jr, von Kobbe C, Sommers JA, Karmakar P, Opresko PL, Piotrowski J, Dianova I, Dianov GL, Bohr VA (2001b) Werner syndrome protein interacts with human flap endonuclease 1 and stimulates its cleavage activity. EMBO J 20:5791–5801
5. Brosh RM Jr, Waheed J, Sommers JA (2002) Biochemical characterization of the DNA substrate specificity of Werner syndrome helicase. J Biol Chem 277:23236–23245
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2. WRN promotes bone development and growth by unwinding SHOX-G-quadruplexes via its helicase activity in Werner Syndrome;Nature Communications;2022-09-16
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