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Molecular and Cellular Biology, January 2009, p. 483-492, Vol. 29, No. 2
0270-7306/09/$08.00+0     doi:10.1128/MCB.01525-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

Rad50 Is Dispensable for the Maintenance and Viability of Postmitotic Tissues ^,

Carrie A. Adelman,^1,2 Saurav De,¹ and John H. J. Petrini^1,2*

Molecular Biology and Genetics, Sloan-Kettering Institute, New York, New York,¹ Weill Cornell Graduate School of Medical Science, New York, New York²

Received 30 September 2008/ Returned for modification 21 October 2008/ Accepted 28 October 2008

The majority of spontaneous chromosome breakage occurs during the process of DNA replication. Homologous recombination is the primary mechanism of repair of such damage, which probably accounts for the fact that it is essential for genome integrity and viability in mammalian cells. The Mre11 complex plays diverse roles in the maintenance of genomic integrity, influencing homologous recombination, checkpoint activation, and telomere maintenance. The complex is essential for cellular viability, but given its myriad influences on genomic integrity, the mechanistic basis for the nonviability of Mre11 complex-deficient cells has not been defined. In this study we generated mice carrying a conditional allele of Rad50 and examined the effects of Rad50 deficiency in proliferative and nonproliferative settings. Depletion of Rad50 in cultured cells caused extensive DNA damage and death within 3 to 5 days of Rad50 deletion. This was not associated with gross telomere dysfunction, suggesting that the telomeric functions of the Mre11 complex are not required for viability. Rad50 was also dispensable for the viability of quiescent liver and postmitotic Purkinje cells of the cerebellum. These findings support the idea that the essential functions of the Mre11 complex are associated with DNA replication and further suggest that homologous recombination is not essential in nondividing cells.

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* Corresponding author. Mailing address: Laboratory of Chromosome Biology, Memorial Sloan-Kettering Cancer Center, 1275 York Avenue, RRL 901C Box 474, New York, NY 10021. Phone: (212) 639-2927. Fax: (646) 422-2062. E-mail: petrinij{at}mskcc.org

Published ahead of print on 10 November 2008.

Supplemental material for this article may be found at http://mcb.asm.org/.

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Molecular and Cellular Biology, January 2009, p. 483-492, Vol. 29, No. 2
0270-7306/09/$08.00+0     doi:10.1128/MCB.01525-08
Copyright © 2009, American Society for Microbiology. All Rights Reserved.

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