AI Article Synopsis

  • Spo11 or related proteins are crucial for forming DNA double-strand breaks (DSBs) during meiosis in various organisms.
  • Researchers discovered a new recombination pathway (Rec*) that can function without Rec12, restoring meiotic processes in certain mutant strains.
  • Rad2, a protein not typically associated with meiotic recombination, appears to play a role by allowing the initiation of recombination through non-DSB DNA issues rather than the standard DSB approach.

Article Abstract

Spo11 or a homologous protein appears to be essential for meiotic DNA double-strand break (DSB) formation and recombination in all organisms tested. We report here the first example of an alternative, mutationally activated pathway for meiotic recombination in the absence of Rec12, the Spo11 homolog of Schizosaccharomyces pombe. Rad2, a FEN-1 flap endonuclease homolog, is involved in processing Okazaki fragments. In its absence, meiotic recombination and proper segregation of chromosomes were restored in rec12Delta mutants to nearly wild-type levels. Although readily detectable in wild-type strains, meiosis-specific DSBs were undetectable in recombination-proficient rad2Delta rec12Delta strains. On the basis of the biochemical properties of Rad2, we propose that meiotic recombination by this alternative (Rec*) pathway can be initiated by non-DSB lesions, such as nicks and gaps, which accumulate during premeiotic DNA replication in the absence of Okazaki fragment processing. We compare the Rec* pathway to alternative pathways of homologous recombination in other organisms.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1456079PMC
http://dx.doi.org/10.1534/genetics.105.046821DOI Listing

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