Abstract
<jats:p>During meiosis, programmed DNA double-strand breaks (DSBs) are repaired with the homolog to form crossovers (COs) essential for chromosome segregation, or noncrossovers (nCOs) to restore genomic integrity. Only a few recombination intermediates will become COs and these sites are progressively enriched in proCO factors at the expense of nCO sites, referred to as coarsening. Here, we show that in C. elegans this process is engineered by ZHP-2/HEI10, a conserved E3 ligase that has functions at early and late stages of CO formation. Early on, ZHP-2-mediated loss of RMH-1/RMI1 and HIM-6/BLM from strand exchange intermediates is required for joint molecule formation and nCO repair. In zhp-2 mutants, proCO factors accumulate at HR sites, leading to defects in CO formation and CO spacing. We find that Polo kinase recruitment to a ZHP-2 at CO precursors signals an end to further DSB formation, and triggers proCO factor coarsening and CO formation. We propose that ZHP-2 disassembles proCO factors from recombination intermediates until it is inactivated at CO precursors through Polo kinase recruitment, leading to stabilization of proCO factors, and resolution of joint molecules as crossovers. Our study reveals that ZHP-2/HEI10 is the central component of a Polo kinase-driven switch that initiates proCO factor coarsening and execution of crossing over.</jats:p>