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Crossing Over Is Rarely Associated With Mitotic Intragenic Recombination in Schizosaccharomyces pombe
Jeffrey B. Virgina,b, Jeffrey P. Baileya, Farnaz Hasteha, James Nevillea, Amy Colea, and Gerard Trompba Department of Pathology, Wayne State University and the Barbara Ann Karmanos Cancer Institute, Detroit, Michigan
b Center for Molecular Medicine and Genetics, Wayne State University and the Barbara Ann Karmanos Cancer Institute, Detroit, Michigan
Corresponding author: Jeffrey B. Virgin, Department of Pathology, University of Washington, VA Medical Ctr., 1660 S. Columbian Way, Seattle, WA 90108., jvirgin{at}u.washington.edu (E-mail)
Communicating editor: L. S. SYMINGTON
14 x 10-6 recombinants per cell generation, similar to allelic recombination rates in diploids. In contrast, ectopic recombination rates in heterozygous diploids were 2.570 times lower than allelic recombination or ectopic recombination in haploids. These results suggest that diploid-specific factors inhibit ectopic recombination. Very few crossovers occurred in ade6 mitotic recombination, either allelic or ectopic. Allelic intragenic recombination was associated with 2% crossing over, and ectopic recombination between multiple different pairing partners showed 17% crossing over. These results contrast sharply with the 3565% crossovers associated with meiotic ade6 recombination and suggest either differential control of resolution of recombination intermediates or alternative pathways of recombination in mitosis and meiosis.
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