Key result
A transgene insertion expressing GFP::COSA-1 suppressed the crossover deficit caused by a partial reduction in MutSγ function.
COSA-1 promotes crossover formation, at least in part, through positive regulation of MutSγ function.
Indicates COSA-1 positively regulates MutSγ for crossover formation; extends meiotic models but leaves open conservation in mammals.
Meiotic crossover formation requires the activity of multiple pro-crossover factors, including the MutSγ complex and the cyclin-related protein COSA-1, that become concentrated together at the sites of crossover recombination intermediates. Here we show that a transgene insertion expressing GFP::COSA-1 can suppress the crossover deficit caused by a partial reduction in MutSγ function. Our data, combined with previous findings, support a model in which COSA-1 promotes crossover formation, at least in part, through positive regulation of MutSγ function.
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Girard et al. (2021) studied Meiotic crossover deficit. Transgene insertion expressing GFP::COSA-1 was evaluated on Crossover deficit caused by a partial reduction in MutSγ function. A transgene insertion expressing GFP::COSA-1 suppressed the crossover deficit caused by a partial reduction in MutSγ function.
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