Involvement of Mammalian Mus81 in Genome Integrity and Tumor Suppression

Author:

McPherson John Peter12345,Lemmers Bénédicte12345,Chahwan Richard12345,Pamidi Ashwin12345,Migon Eva12345,Matysiak-Zablocki Elzbieta12345,Moynahan Mary Ellen12345,Essers Jeroen12345,Hanada Katsuhiro12345,Poonepalli Anuradha12345,Sanchez-Sweatman Otto12345,Khokha Rama12345,Kanaar Roland12345,Jasin Maria12345,Hande M. Prakash12345,Hakem Razqallah12345

Affiliation:

1. Ontario Cancer Institute, 620 University Avenue, Suite 706, Toronto, Ontario, Canada M5G 2C1.

2. Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada M5G 2M9.

3. Department of Medicine, Memorial Sloan-Kettering Cancer Center, New York, NY 10021, USA.

4. Department of Cell Biology and Genetics, and Department of Radiation Oncology, Erasmus MC (University Medical Center), Post Office Box 1738, 3000 DR Rotterdam, Netherlands.

5. Department of Physiology and Oncology Research Institute, Faculty of Medicine, National University of Singapore, Singapore 117597.

Abstract

Mus81-Eme1 endonuclease has been implicated in the rescue of stalled replication forks and the resolution of meiotic recombination intermediates in yeast. We used gene targeting to study the physiological requirements of Mus81 in mammals. Mus81 –/– mice are viable and fertile, which indicates that mammalian Mus81 is not essential for recombination processes associated with meiosis. Mus81-deficient mice and cells were hypersensitive to the DNA cross-linking agent mitomycin C but not to γ-irradiation. Remarkably, both homozygous Mus81 –/– and heterozygous Mus81 +/– mice exhibited a similar susceptibility to spontaneous chromosomal damage and a profound and equivalent predisposition to lymphomas and other cancers. These studies demonstrate a critical role for the proper biallelic expression of the mammalian Mus81 in the maintenance of genomic integrity and tumor suppression.

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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