61
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      The Drosophila Genome Nexus: A Population Genomic Resource of 623 Drosophila melanogaster Genomes, Including 197 from a Single Ancestral Range Population

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Hundreds of wild-derived Drosophila melanogaster genomes have been published, but rigorous comparisons across data sets are precluded by differences in alignment methodology. The most common approach to reference-based genome assembly is a single round of alignment followed by quality filtering and variant detection. We evaluated variations and extensions of this approach and settled on an assembly strategy that utilizes two alignment programs and incorporates both substitutions and short indels to construct an updated reference for a second round of mapping prior to final variant detection. Utilizing this approach, we reassembled published D. melanogaster population genomic data sets and added unpublished genomes from several sub-Saharan populations. Most notably, we present aligned data from phase 3 of the Drosophila Population Genomics Project (DPGP3), which provides 197 genomes from a single ancestral range population of D. melanogaster (from Zambia). The large sample size, high genetic diversity, and potentially simpler demographic history of the DPGP3 sample will make this a highly valuable resource for fundamental population genetic research. The complete set of assemblies described here, termed the Drosophila Genome Nexus, presently comprises 623 consistently aligned genomes and is publicly available in multiple formats with supporting documentation and bioinformatic tools. This resource will greatly facilitate population genomic analysis in this model species by reducing the methodological differences between data sets.

          Related collections

          Most cited references25

          • Record: found
          • Abstract: found
          • Article: not found

          Chromosome inversions, local adaptation and speciation.

          We study the evolution of inversions that capture locally adapted alleles when two populations are exchanging migrants or hybridizing. By suppressing recombination between the loci, a new inversion can spread. Neither drift nor coadaptation between the alleles (epistasis) is needed, so this local adaptation mechanism may apply to a broader range of genetic and demographic situations than alternative hypotheses that have been widely discussed. The mechanism can explain many features observed in inversion systems. It will drive an inversion to high frequency if there is no countervailing force, which could explain fixed differences observed between populations and species. An inversion can be stabilized at an intermediate frequency if it also happens to capture one or more deleterious recessive mutations, which could explain polymorphisms that are common in some species. This polymorphism can cycle in frequency with the changing selective advantage of the locally favored alleles. The mechanism can establish underdominant inversions that decrease heterokaryotype fitness by several percent if the cause of fitness loss is structural, while if the cause is genic there is no limit to the strength of underdominance that can result. The mechanism is expected to cause loci responsible for adaptive species-specific differences to map to inversions, as seen in recent QTL studies. We discuss data that support the hypothesis, review other mechanisms for inversion evolution, and suggest possible tests.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: found
            Is Open Access

            Natural variation in genome architecture among 205 Drosophila melanogaster Genetic Reference Panel lines

            The Drosophila melanogaster Genetic Reference Panel (DGRP) is a community resource of 205 sequenced inbred lines, derived to improve our understanding of the effects of naturally occurring genetic variation on molecular and organismal phenotypes. We used an integrated genotyping strategy to identify 4,853,802 single nucleotide polymorphisms (SNPs) and 1,296,080 non-SNP variants. Our molecular population genomic analyses show higher deletion than insertion mutation rates and stronger purifying selection on deletions. Weaker selection on insertions than deletions is consistent with our observed distribution of genome size determined by flow cytometry, which is skewed toward larger genomes. Insertion/deletion and single nucleotide polymorphisms are positively correlated with each other and with local recombination, suggesting that their nonrandom distributions are due to hitchhiking and background selection. Our cytogenetic analysis identified 16 polymorphic inversions in the DGRP. Common inverted and standard karyotypes are genetically divergent and account for most of the variation in relatedness among the DGRP lines. Intriguingly, variation in genome size and many quantitative traits are significantly associated with inversions. Approximately 50% of the DGRP lines are infected with Wolbachia , and four lines have germline insertions of Wolbachia sequences, but effects of Wolbachia infection on quantitative traits are rarely significant. The DGRP complements ongoing efforts to functionally annotate the Drosophila genome. Indeed, 15% of all D. melanogaster genes segregate for potentially damaged proteins in the DGRP, and genome-wide analyses of quantitative traits identify novel candidate genes. The DGRP lines, sequence data, genotypes, quality scores, phenotypes, and analysis and visualization tools are publicly available.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Massive genomic variation and strong selection in Arabidopsis thaliana lines from Sweden.

              Despite advances in sequencing, the goal of obtaining a comprehensive view of genetic variation in populations is still far from reached. We sequenced 180 lines of A. thaliana from Sweden to obtain as complete a picture as possible of variation in a single region. Whereas simple polymorphisms in the unique portion of the genome are readily identified, other polymorphisms are not. The massive variation in genome size identified by flow cytometry seems largely to be due to 45S rDNA copy number variation, with lines from northern Sweden having particularly large numbers of copies. Strong selection is evident in the form of long-range linkage disequilibrium (LD), as well as in LD between nearby compensatory mutations. Many footprints of selective sweeps were found in lines from northern Sweden, and a massive global sweep was shown to have involved a 700-kb transposition.
                Bookmark

                Author and article information

                Journal
                Genetics
                Genetics
                genetics
                genetics
                genetics
                Genetics
                Genetics Society of America
                0016-6731
                1943-2631
                April 2015
                27 January 2015
                27 January 2015
                : 199
                : 4
                : 1229-1241
                Affiliations
                [* ]Laboratory of Genetics, University of Wisconsin, Madison, Wisconsin 53706
                []Department of Evolution and Ecology, University of California, Davis, California 95616
                []Department of Computer Sciences, University of Wisconsin, Madison, Wisconsin 53706
                [§ ]Department of Integrative Biology, University of California, Berkeley, California 94720
                [** ]Department of Statistics, University of California, Berkeley, California 94720
                Author notes
                [1 ]Corresponding authors: 5302 Genetics/Biotechnology Bldg., Laboratory of Genetics, University of Wisconsin, 425-G Henry Mall, Madison, WI 53706. E-mail: jlack@ 123456wisc.edu ; 3342B Storer Hall, Center for Population Biology and Department of Evolution and Ecology, University of California, One Shields Ave., Davis, CA 95616-8554. E-mail: chlangley@ 123456ucdavis.edu ; 5302 Genetics/Biotechnology Bldg., Laboratory of Genetics, University of Wisconsin, 425-G Henry Mall, Madison, WI 53706. E-mail: jpool@ 123456wisc.edu
                Article
                174664
                10.1534/genetics.115.174664
                4391556
                25631317
                8eb789ac-f60d-43b8-ac74-a633b89e7f76
                Copyright © 2015 by the Genetics Society of America

                Available freely online through the author-supported open access option.

                History
                : 02 October 2014
                : 23 January 2015
                Page count
                Pages: 13
                Categories
                Investigations
                Population and Evolutionary Genetics
                Custom metadata
                highlight-article

                Genetics
                drosophila melanogaster,population genomics,genome assembly,drosophila genome nexus
                Genetics
                drosophila melanogaster, population genomics, genome assembly, drosophila genome nexus

                Comments

                Comment on this article