Multiple start codons and phosphorylation result in discrete Rad52 protein species

• Published in: Nucleic acids research 2006-01, Vol.34 (9), p.2587-2597
• Main Authors: de Mayolo, Adriana Antúnez, Lisby, Michael, Erdeniz, Naz, Thybo, Tanja, Mortensen, Uffe H., Rothstein, Rodney
• Format: Article
• Language: English
• Subjects: Alleles; Amino Acid Sequence; Cell Cycle; Codon, Initiator; Molecular Sequence Data; Mutation; Phosphorylation; Protein Processing, Post-Translational; Rad52 DNA Repair and Recombination Protein - chemistry; Rad52 DNA Repair and Recombination Protein - genetics; Rad52 DNA Repair and Recombination Protein - metabolism; Recombination, Genetic; Saccharomyces cerevisiae - genetics; Saccharomyces cerevisiae Proteins - chemistry; Saccharomyces cerevisiae Proteins - genetics; Saccharomyces cerevisiae Proteins - metabolism
• ISSN: 0305-1048; 1362-4962
• DOI: 10.1093/nar/gkl280

The sequence of the Saccharomyces cerevisiae RAD52 gene contains five potential translation start sites and protein-blot analysis typically detects multiple Rad52 species with different electrophoretic mobilities. Here we define the gene products encoded by RAD52. We show that the multiple Rad52 protein species are due to promiscuous choice of start codons as well as post-translational modification. Specifically, Rad52 is phosphorylated both in a cell cycle-independent and in a cell cycle-dependent manner. Furthermore, phosphorylation is dependent on the presence of the Rad52 C terminus, but not dependent on its interaction with Rad51. We also show that the Rad52 protein can be translated from the last three start sites and expression from any one of them is sufficient for spontaneous recombination and the repair of gamma-ray-induced double-strand breaks.