This Article Full Text Full Text (PDF) Alert me when this article is cited Alert me if a correction is posted Services Similar articles in this journal Similar articles in PubMed Alert me to new issues of the journal Download to citation manager Copyright Information Books from ASM Press MicrobeWorld Citing Articles Citing Articles via Google Scholar Google Scholar Articles by Shalguev, V. I. Articles by Lanzov, V. A. Search for Related Content PubMed PubMed Citation Articles by Shalguev, V. I. Articles by Lanzov, V. A.

Rad51 Protein from the Thermotolerant Yeast Pichia angusta as a Typical but Thermodependent Member of the Rad51 Family

Valery I. Shalguev, Yury V. Kil, Ludmila V. Yurchenko, Eugene A. Namsaraev, and Vladislav A. Lanzov^*

Division of Molecular and Radiation Biophysics, Petersburg Nuclear Physics Institute, Russian Academy of Sciences, Gatchina/St. Petersburg, Russia

Received 16 June 2004/ Accepted 9 September 2004

The Rad51 protein from the methylotrophic yeast Pichia angusta (Rad51_Pa) of the taxonomic complex Hansenula polymorpha is a homolog of the RecA-RadA-Rad51 protein superfamily, which promotes homologous recombination and recombination repair in prokaryotes and eukaryotes. We cloned the RAD51 gene from the cDNA library of the thermotolerant P. angusta strain BKM Y1397. Induction of this gene in a rad51-deficient Saccharomyces cerevisiae strain partially complemented the survival rate after ionizing radiation. Purified Rad51_Pa protein exhibited properties typical of the superfamily, including the stoichiometry of binding to single-stranded DNA (ssDNA) (one protomer of Rad51_Pa per 3 nucleotides) and DNA specificity for ssDNA-dependent ATP hydrolysis [poly(dC) > poly(dT) > X174 ssDNA > poly(dA) > double-stranded M13 DNA]. An inefficient ATPase and very low cooperativity for ATP interaction position Rad51_Pa closer to Rad51 than to RecA. Judging by thermoinactivation, Rad51_Pa alone was 20-fold more thermostable at 37°C than its S. cerevisiae homolog (Rad51_Sc). Moreover, it maintained ssDNA-dependent ATPase and DNA transferase activities up to 52 to 54°C, whereas Rad51_Sc was completely inactive at 47°C. A quick nucleation and an efficient final-product formation in the strand exchange reaction promoted by Rad51_Pa occurred only at temperatures above 42°C. These reaction characteristics suggest that Rad51_Pa is dependent on high temperatures for activity.

Present address: Stanford Genome Technology Center, Stanford University, Palo Alto, CA 94304.