| Literature DB >> 12955454 |
Alexandra L Grishchuk1, Rolf Kraehenbuehl, Monika Molnar, Oliver Fleck, Juerg Kohli.
Abstract
The Schizosaccharomyces pombe rad51(+) and dmc1(+) genes code for homologues of the Escherichia coli recombination protein RecA. Deletion of rad51(+) causes slow growth, retardation of cell division and a decrease in viability. rad51Delta cells have a defect in mating-type switching. The DNA modification at the mating-type locus required for mating-type switching contributes to slow growth in the rad51 mutant. Cell mating is reduced in crosses homozygous for rad51Delta. Ectopic expression of the dmc1(+) gene allowed us to demonstrate that the reduction in meiotic recombination in dmc1 mutants is not caused by a disturbance of rad24 expression from the dmc1- rad24 bicistronic RNA. We describe the functional defects of terminally epitope-tagged Dmc1 and Rad51 and discuss it in terms of protein interaction. Presumptive Rad51 and Dmc1 foci were detected on spreads of meiotic chromatin.Entities:
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Year: 2003 PMID: 12955454 DOI: 10.1007/s00294-003-0439-7
Source DB: PubMed Journal: Curr Genet ISSN: 0172-8083 Impact factor: 3.886