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Genomic Variation in Natural Populations ofDrosophila melanogaster
Author(s) -
Charles H. Langley,
Kristian Stevens,
Charis Cardeno,
Yuh Chwen G. Lee,
Daniel R. Schrider,
John E. Pool,
Sasha A. Langley,
Charlyn Suarez,
Russell CorbettDetig,
Bryan Kolaczkowski,
Shu Fang,
Phillip M Nista,
Alisha K. Holloway,
Andrew D. Kern,
Colin N. Dewey,
Yun S. Song,
Matthew W. Hahn,
David J. Begun
Publication year - 2012
Publication title -
genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.792
H-Index - 246
eISSN - 1943-2631
pISSN - 0016-6731
DOI - 10.1534/genetics.112.142018
Subject(s) - biology , genetics , nonsynonymous substitution , natural selection , evolutionary biology , genome , linkage disequilibrium , genome evolution , population , gene density , allele , haplotype , gene , demography , sociology
This report of independent genome sequences of two natural populations of Drosophila melanogaster (37 from North America and 6 from Africa) provides unique insight into forces shaping genomic polymorphism and divergence. Evidence of interactions between natural selection and genetic linkage is abundant not only in centromere- and telomere-proximal regions, but also throughout the euchromatic arms. Linkage disequilibrium, which decays within 1 kbp, exhibits a strong bias toward coupling of the more frequent alleles and provides a high-resolution map of recombination rate. The juxtaposition of population genetics statistics in small genomic windows with gene structures and chromatin states yields a rich, high-resolution annotation, including the following: (1) 5'- and 3'-UTRs are enriched for regions of reduced polymorphism relative to lineage-specific divergence; (2) exons overlap with windows of excess relative polymorphism; (3) epigenetic marks associated with active transcription initiation sites overlap with regions of reduced relative polymorphism and relatively reduced estimates of the rate of recombination; (4) the rate of adaptive nonsynonymous fixation increases with the rate of crossing over per base pair; and (5) both duplications and deletions are enriched near origins of replication and their density correlates negatively with the rate of crossing over. Available demographic models of X and autosome descent cannot account for the increased divergence on the X and loss of diversity associated with the out-of-Africa migration. Comparison of the variation among these genomes to variation among genomes from D. simulans suggests that many targets of directional selection are shared between these species.

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