ATM phosphorylation of Nijmegen breakage syndrome protein is required in a DNA damage response View Full Text


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Article Info

DATE

2000-05

AUTHORS

Xiaohua Wu, Velvizhi Ranganathan, David S. Weisman, Walter F. Heine, David N. Ciccone, Ted B. O'Neill, Kindra E. Crick, Kerry A. Pierce, William S. Lane, Gary Rathbun, David M. Livingston, David T. Weaver

ABSTRACT

Nijmegen breakage syndrome (NBS) is characterized by extreme radiation sensitivity, chromosomal instability and cancer. The phenotypes are similar to those of ataxia telangiectasia mutated (ATM) disease, where there is a deficiency in a protein kinase that is activated by DNA damage, indicating that the Nbs and Atm proteins may participate in common pathways. Here we report that Nbs is specifically phosphorylated in response to gamma-radiation, ultraviolet light and exposure to hydroxyurea. Phosphorylation of Nbs mediated by gamma-radiation, but not that induced by hydroxyurea or ultraviolet light, was markedly reduced in ATM cells. In vivo, Nbs was phosphorylated on many serine residues, of which S343, S397 and S615 were phosphorylated by Atm in vitro. At least two of these sites were underphosphorylated in ATM cells. Inactivation of these serines by mutation partially abrogated Atm-dependent phosphorylation. Reconstituting NBS cells with a mutant form of Nbs that cannot be phosphorylated at selected, ATM-dependent serine residues led to a specific reduction in clonogenic survival after gamma-radiation. Thus, phosphorylation of Nbs by Atm is critical for certain responses of human cells to DNA damage. More... »

PAGES

477

References to SciGraph publications

Identifiers

URI

http://scigraph.springernature.com/pub.10.1038/35013089

DOI

http://dx.doi.org/10.1038/35013089

DIMENSIONS

https://app.dimensions.ai/details/publication/pub.1036110211

PUBMED

https://www.ncbi.nlm.nih.gov/pubmed/10839545


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