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Despite many years of theoretical and experimental work, the explanation for why sex is so common as a reproductive strategy continues to resist understanding. Recent empirical work has addressed key questions in this field, especially regarding rates of mutation accumulation in sexual and asexual organisms, and the roles of negative epistasis and drift as sources of adaptive constraint in asexually reproducing organisms. At the same time, new ideas about the evolution of sexual recombination are being tested, including intriguing suggestions of an important interplay between sex and genetic architecture, which indicate that sex and recombination could have affected their own evolution.
Drift, Evolution, Mutation accumulation, deleterious mutations, synergistic epistasis, mullers ratchet, Models, Biological, Linkage Disequilibrium, yeast saccharomyces-cerevisiae, polygenes controlling viability, Negative epistasis, Reproduction, Asexual, Sexual reproduction, Selection, Genetic, drosophila-melanogaster, Genome, Models, Genetic, Genetic Drift, Epistasis, Genetic, Biological Evolution, beneficial mutations, caenorhabditis-elegans, escherichia-coli, Sex, Recombinational load, natural-selection
Drift, Evolution, Mutation accumulation, deleterious mutations, synergistic epistasis, mullers ratchet, Models, Biological, Linkage Disequilibrium, yeast saccharomyces-cerevisiae, polygenes controlling viability, Negative epistasis, Reproduction, Asexual, Sexual reproduction, Selection, Genetic, drosophila-melanogaster, Genome, Models, Genetic, Genetic Drift, Epistasis, Genetic, Biological Evolution, beneficial mutations, caenorhabditis-elegans, escherichia-coli, Sex, Recombinational load, natural-selection
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