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Vol. 15, Issue 1, 71-80, January 2004
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* 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 13, 2003;
Revised September 5, 2003;
Accepted September 6, 2003
Monitoring Editor: Trisha Davis
In most eukaryotes, genes encoding ribosomal RNAs (rDNA) are clustered in long tandem head-to-tail repeats. Studies of Saccharomyces cerevisiae have indicated that rDNA copy number is maintained through recombination events associated with site-specific blockage of replication forks (RFs). Here, we describe two Schizosaccharomyces pombe proteins, homologs of S. cerevisiae Slx1 and Slx4, as subunits of a novel type of endonuclease that maintains rDNA copy number. The Slx1-Slx4dependent endonuclease introduces single-strand cuts in duplex DNA on the 3' side of junctions with single-strand DNA. Deletion of Slx1 or Rqh1 RecQ-like DNA helicase provokes rDNA contraction, whereas simultaneous elimination of Slx1-Slx4 endonuclease and Rqh1 is lethal. Slx1 associates with chromatin at two foci characteristic of the two rDNA repeat loci in S. pombe. We propose a model in which the Slx1Slx4 complex is involved in the control of the expansion and contraction of the rDNA loci by initiating recombination events at stalled RFs.
These authors contributed equally to this work.
Corresponding author. E-mail address: prussell{at}scripps.edu.
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