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Eukaryotic Cell, July 2005, p. 1239-1252, Vol. 4, No. 7
1535-9778/05/$08.00+0 doi:10.1128/EC.4.7.1239-1252.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.
Camile P. Semighini,2,
Iran Malavazi,1
Marcela Savoldi,1
Joel Fernandes de Lima,1
Maria Helena de Souza Goldman,3
Steven D. Harris,2 and
Gustavo Henrique Goldman1*
Faculdade de Ciências Farmacêuticas de Ribeirão Preto,1 Faculdade de Filosofia, Ciências e Letras de Ribeirão Preto, Universidade de São Paulo, São Paulo, Brazil,3 Plant Science Initiative, University of Nebraska, N234 Beadle Center, Lincoln, Nebraska 68588-06602
Received 22 February 2005/ Accepted 19 April 2005
The ATM/ATR kinases and the Mre11 (Mre11-Rad50-Nbs1) protein complex are central players in the cellular DNA damage response. Here we characterize possible interactions between Aspergillus nidulans uvsBATR and the Mre11 complex (scaANBS1). We demonstrate that there is an epistatic relationship between uvsBATR, the homolog of the ATR/MEC1 gene, and scaANBS1, the homolog of the NBS1/XRS2 gene, for both repair and checkpoint functions and that correct ScaANBS1 expression during recovery from replication stress depends on uvsBATR. In addition, we also show that the formation of UvsC foci during recovery from replication stress is dependent on both uvsBATR and scaANBS1 function. Furthermore, ScaANBS1 is also dependent on uvsBATR for nuclear focus formation upon the induction of DNA double-strand breaks by phleomycin. Our results highlight the extensive genetic interactions between UvsB and the Mre11 complex that are required for S-phase progression and recovery from DNA damage.
Both authors contributed equally to this work.
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