Rad22 protein, a Rad52 homologue in Schizosaccharomyces pombe, binds to DNA double-strand breaks

Woo Jae Kim, Suman Lee, Min Sung Park, Yeun Kyu Jang, Jae Bum Kim, Sang Dai Park

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

DNA double-strand breaks can be introduced by exogenous agents or during normal cellular processes. Genes belonging to the RAD52 eplstasis group are known to repair these breaks in budding yeast. Among these genes, RAD52 plays a central role in homologous recombination and DNA double-strand break repair. Despite its importance, its mechanism of action is not yet clear. It is known, however, that the human homologue of Rad52 is capable of binding to DNA ends in vitro. Herein, we show that Rad22 protein, a Rad52 homologue in the fission yeast Schizosaccharomyces pombe, can similarly bind to DNA ends at double-strand breaks. This end-binding ability was demonstrated in vitro by electron microscopy and by protection from exonuclease attack. We also showed that Rad22 specifically binds near double-strand break associated with mating type switching in vivo by chromatin immunoprecipitation analysis. This is the first evidence that a recombinational protein directly binds to DNA double-strand breaks in vivo.

Original languageEnglish
Pages (from-to)35607-35611
Number of pages5
JournalJournal of Biological Chemistry
Volume275
Issue number45
DOIs
Publication statusPublished - 2000 Nov 10

Fingerprint

Rad52 DNA Repair and Recombination Protein
Double-Stranded DNA Breaks
Schizosaccharomyces
DNA
Exonucleases
Proteins
Saccharomycetales
Chromatin Immunoprecipitation
Homologous Recombination
Yeast
Repair
Genes
Electron Microscopy
Electron microscopy
Chromatin
In Vitro Techniques

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Molecular Biology
  • Cell Biology

Cite this

Kim, Woo Jae ; Lee, Suman ; Park, Min Sung ; Jang, Yeun Kyu ; Kim, Jae Bum ; Park, Sang Dai. / Rad22 protein, a Rad52 homologue in Schizosaccharomyces pombe, binds to DNA double-strand breaks. In: Journal of Biological Chemistry. 2000 ; Vol. 275, No. 45. pp. 35607-35611.
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abstract = "DNA double-strand breaks can be introduced by exogenous agents or during normal cellular processes. Genes belonging to the RAD52 eplstasis group are known to repair these breaks in budding yeast. Among these genes, RAD52 plays a central role in homologous recombination and DNA double-strand break repair. Despite its importance, its mechanism of action is not yet clear. It is known, however, that the human homologue of Rad52 is capable of binding to DNA ends in vitro. Herein, we show that Rad22 protein, a Rad52 homologue in the fission yeast Schizosaccharomyces pombe, can similarly bind to DNA ends at double-strand breaks. This end-binding ability was demonstrated in vitro by electron microscopy and by protection from exonuclease attack. We also showed that Rad22 specifically binds near double-strand break associated with mating type switching in vivo by chromatin immunoprecipitation analysis. This is the first evidence that a recombinational protein directly binds to DNA double-strand breaks in vivo.",
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Rad22 protein, a Rad52 homologue in Schizosaccharomyces pombe, binds to DNA double-strand breaks. / Kim, Woo Jae; Lee, Suman; Park, Min Sung; Jang, Yeun Kyu; Kim, Jae Bum; Park, Sang Dai.

In: Journal of Biological Chemistry, Vol. 275, No. 45, 10.11.2000, p. 35607-35611.

Research output: Contribution to journalArticle

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AU - Lee, Suman

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