The Mre11-Nbs1 Interface Is Essential for Viability and Tumor Suppression

• Main Authors: Jun Hyun Kim, Malgorzata Grosbart, Roopesh Anand, Claire Wyman, Petr Cejka, John H.J. Petrini
• Format: Article
• Language: English
• Published: Elsevier 2017-01-01
• Series: Cell Reports
• Online Access: http://www.sciencedirect.com/science/article/pii/S2211124716317259

Summary: The Mre11 complex (Mre11, Rad50, and Nbs1) is integral to both DNA repair and ataxia telangiectasia mutated (ATM)-dependent DNA damage signaling. All three Mre11 complex components are essential for viability at the cellular and organismal levels. To delineate essential and non-essential Mre11 complex functions that are mediated by Nbs1, we used TALEN-based genome editing to derive Nbs1 mutant mice (Nbs1mid mice), which harbor mutations in the Mre11 interaction domain of Nbs1. Nbs1mid alleles that abolished interaction were incompatible with viability. Conversely, a 108-amino-acid Nbs1 fragment comprising the Mre11 interface was sufficient to rescue viability and ATM activation in cultured cells and support differentiation of hematopoietic cells in vivo. These data indicate that the essential role of Nbs1 is via its interaction with Mre11 and that most of the Nbs1 protein is dispensable for Mre11 complex functions and suggest that Mre11 and Rad50 directly activate ATM. : Kim et al. find that Nbs1 promotes the proper assembly and localization of a complex containing Mre11 and Rad50. Nbs1-mediated assembly is required for the function of the complex, and a 108-amino-acid Nbs1 fragment containing the Mre11 interaction domain is sufficient for this essential role. Keywords: Nbs1mid mutants, Mre11-Nbs1 interface, ATM activation, Mre11 complex assembly