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As two species diverge from one another, they become increasingly isolated by reproductive incompatibilities. New findings, however, undermine this evolutionary orthodoxy, showing that the first identified mammal speciation gene causes only transient incompatibility between diverging species.

Crossing over between homologous chromosomes during meiosis repairs programmed DNA double-strand breaks, ensures proper segregation at meiosis I [1], shapes the genomic distribution of nucleotide variability in populations, and enhances the efficacy of natural selection among genetically linked sites [2]. Between closely related Drosophila species, large differences exist in the rate and chromosomal distribution of crossing over. Little, however, is known about the molecular genetic changes or population genetic forces that mediate evolved differences in recombination between species [3, 4]. Here, we show that a meiosis gene with a history of rapid evolution acts as a trans-acting modifier of species differences in crossing over. In transgenic flies, the dicistronic gene, mei-217/mei-218, recapitulates a large part of the species differences in the rate and chromosomal distribution of crossing over. These phenotypic differences appear to result from changes in protein sequence not gene expression. Our population genetics analyses show that the protein-coding sequence of mei-218, but not mei-217, has a history of recurrent positive natural selection. By modulating the intensity of centromeric and telomeric suppression of crossing over, evolution at mei-217/-218 has incidentally shaped gross differences in the chromosomal distribution of nucleotide variability between species. We speculate that recurrent bouts of adaptive evolution at mei-217/-218 might reflect a history of coevolution with selfish genetic elements.

Summary Evolutionary theory predicts that the rate and level of adaptation will be enhanced in sexual relative to asexual genomes because sexual recombination facilitates the elimination of deleterious mutations and the fixation of beneficial ones by natural selection [1–3]. To date, the most compelling evidence for this prediction comes from experimental evolution studies [4] and from loci completely lacking recombination, such as those on Y chromosomes [5], which often show reduced adaptation and even degeneration. Here, by analyzing replacement and silent DNA polymorphism and divergence at 98 loci, I show that recombination increases the efficacy of protein adaptation throughout the genome of the fruit fly Drosophila melanogaster . Genes residing in genomic regions with reduced recombination rates suffer a greater load of segregating, mildly deleterious mutations and fix fewer beneficial mutations than genes residing in regions with higher recombination rates. These findings suggest that the capacity to respond to natural selection varies with recombination rate across the genome, consistent with theory on the evolutionary advantages of sex and recombination.

SummaryHeteromorphic sex chromosomes are thought to represent a terminal evolutionary endpoint due to their specialized gene content and chromosome-specific regulation. New findings, however, show that an ancient X chromosome reverted to an autosome in the lineage leading to Drosophila.

Evolutionary biologists have long recognized that the sterility and inviability of species hybrids must involve incompatible epistatic interactions between two (or more) genes. The first pair of such hybrid incompatibility genes has now been identified.

SummaryOne of the strongest rules of biological diversity — the observation that more species live on large islands than on small ones — is usually attributed to the balance between colonization and extinction. But speciation on islands cannot be ignored.

SummaryTheory predicts that, as species diverge from one another, the number of genetic incompatibilities causing sterility or inviability in interspecies hybrids grows faster than linearly, or snowballs. Two new genetic analyses now provide the first empirical support for this snowball effect.