Jaramillo-Lambert, Aimee
                            (Ed.)
                        
                    
            
                            Meiotic recombination plays an important role in ensuring proper chromosome segregation during meiosis I through the creation of chiasmata that connect homologous chromosomes. Recombination plays an additional role in evolution by creating new allelic combinations. Organisms display species-specific crossover patterns, but how these patterns are established is poorly understood.Drosophila mauritianadisplays a different meiotic recombination pattern compared toDrosophila melanogaster, withD. mauritianaexperiencing a reduced centromere effect, the suppression of recombination emanating from the centromeres. To evaluate the contribution of the synaptonemal complex (SC) C(3)G protein to these recombination rate differences, theD. melanogasterallele was replaced withD. mauritiana c(3)Gcoding sequence. We found that theD. mauritianaC(3)G could interact with theD. melanogasterSC machinery to build full length tripartite SC and chromosomes segregated accurately, indicating sufficient crossovers were generated. However, the placement of crossovers was altered, displaying an increase in frequency in the centromere-proximal euchromatin indicating a decrease in the centromere effect, similar to that observed inD. mauritianafemales. Recovery of chromatids with more than one crossover was also increased, likely due to the larger chromosome span now available for crossovers. As replacement of a single gene mediated a strong shift of one species’ crossover pattern towards another species, it indicates a small number of discrete factors may have major influence on species-specific crossover patterning. Additionally, it demonstrates the SC, a structure known to be required for crossover formation in many species, is likely one of these discrete factors. 
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