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A New Recombinational DNA Repair Gene From Schizosaccharomyces pombe With Homology to Escherichia coli RecA
Fuat K. Khasanova, Galina V. Savchenkoa, Elena V. Bashkirovab, Vladimir G. Korolevc, Wolf-Dietrich Heyerb,d, and Vladimir I. Bashkirova,b,da Institute of Gene Biology, Russian Academy of Sciences, Moscow 117 984, Russia,
b Section of Microbiology, University of California, Davis, California 95616,
c St. Petersburg Nuclear Physics Institute, Gatchina 188 350, Russia
d Institute for General Microbiology, University of Bern, CH-3012 Bern, Switzerland
Corresponding author: Wolf-Dietrich Heyer, Section of Microbiology, University of California, Davis, 1 Shields Ave., Davis, CA 95616., wdheyer{at}ucdavis.edu (E-mail)
Communicating editor: L. S. SYMINGTON
mutant was highly sensitive to methyl methanesulfonate (MMS), ionizing radiation (IR), and, to a lesser degree, UV. These phenotypes were enhanced at low temperatures, similar to deletions in the S. cerevisiae RAD55 and RAD57 genes. Many rhp55
cells were elongated with aberrant nuclei and an increased DNA content. The rhp55 mutant showed minor deficiencies in meiotic intra- and intergenic recombination. Sporulation efficiency and spore viability were significantly reduced. Double-mutant analysis showed that rhp55+ acts in one DNA repair pathway with rhp51+ and rhp54+, homologs of the budding yeast RAD51 and RAD54 genes, respectively. However, rhp55+ is in a different epistasis group for repair of UV-, MMS-, or
-ray-induced DNA damage than is rad22+, a putative RAD52 homolog of fission yeast. The structural and functional similarity suggests that rhp55+ is a homolog of the S. cerevisiae RAD55 gene and we propose that the functional diversification of RecA-like genes in budding yeast is evolutionarily conserved.
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