Cloning of human and mouse genes homologous to RAD52, a yeast gene involved in DNA repair and recombination

Daan F.R. Muris, Olga Bezzubova, Jean Marie Buerstedde, Kees Vreeken, A. S. Balajee, Chris J. Osgood, Christine Troelstra, Jan H.J. Hoeijmakers, Kai Ostermann, Henning Schmidt, A. T. Natarajan, Jan C.J. Eeken, Paul H.M. Lohman, Albert Pastink

Onderzoeksoutput: Bijdrage aan tijdschriftArtikelpeer review

104 Citaten (Scopus)


The RAD52 gene of Saccharomyces cerevisiae is required for recombinational repair of double-strand breaks. Using degenerate oligonucleotides based on conserved amino acid sequences of RAD52 and rad22, its counterpart from Schizosaccharomyces pombe, RAD52 homologs from man and mouse were cloned by the polymerase chain reaction. DNA sequence analysis revealed an open reading frame of 418 amino acids for the human RAD52 homolog and of 420 amino acid residues for the mouse counterpart. The identity between the two proteins is 69% and the overall similarity 80%. The homology of the mammalian proteins with their counterparts from yeast is primarily concentrated in the N-terminal region. Low amounts of RAD52 RNA were observed in adult mouse tissues. A relatively high level of gene expression was observed in testis and thymus, suggesting that the mammalian RAD52 protein, like its homolog from yeast, plays a role in recombination. The mouse RAD52 gene is located near the tip of chromosome 6 in region G3. The human equivalent maps to region p13.3 of chromosome 12. Until now, this human chromosome has not been implicated in any of the rodent mutants with a defect in the repair of double-strand breaks.

Originele taal-2Engels
Pagina's (van-tot)295-305
Aantal pagina's11
TijdschriftMutation Research-DNA Repair
Nummer van het tijdschrift3
StatusGepubliceerd - nov. 1994
Extern gepubliceerdJa


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