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Vol. 15, Issue 2, 552-562, February 2004

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RNA Interference Inhibition of Mus81 Reduces Mitotic Recombination in Human Cells

Veronique Blais ^*, Hui Gao ^*, Cherilyn A. Elwell ^* , Michael N. Boddy ^*, Pierre-Henri L. Gaillard ^*, Paul Russell , and Clare H. McGowan  

^* Department of Molecular Biology, The Scripps Research Institute, La Jolla, California 92037; Department of Cell Biology, The Scripps Research Institute, La Jolla, California 92037

Submitted August 11, 2003; Revised October 15, 2003; Accepted October 15, 2003
Monitoring Editor: Mark Solomon

Mus81 is a highly conserved endonuclease with homology to the XPF subunit of the XPF-ERCC1 complex. In yeast Mus81 associates with a second subunit, Eme1 or Mms4, which is essential for endonuclease activity in vitro and for in vivo function. Human Mus81 binds to a homolog of fission yeast Eme1 in vitro and in vivo. We show that recombinant Mus81-Eme1 cleaves replication forks, 3' flap substrates, and Holliday junctions in vitro. By use of differentially tagged versions of Mus81 and Eme1, we find that Mus81 associates with Mus81 and that Eme1 associates with Eme1. Thus, complexes containing two or more Mus81-Eme1 units could function to coordinate substrate cleavage in vivo. Down-regulation of Mus81 by RNA interference reduces mitotic recombination in human somatic cells. The recombination defect is rescued by expression of a bacterial Holliday junction resolvase. These data provide direct evidence for a role of Mus81-Eme1 in mitotic recombination in higher eukaryotes and support the hypothesis that Mus81-Eme1 resolves Holliday junctions in vivo.

Present address: Department of Medicine, University of California, San Francisco, San Francisco, CA 94143.

Corresponding author. E-mail address: chmcg{at}scripps.edu.

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