11
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Quantifying the contribution of sequence variants with regulatory and evolutionary significance to 34 bovine complex traits

      research-article

      Read this article at

      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.

          Significance

          The extent to which variants with genome regulatory and evolutionary roles affect mammalian phenotypes is unclear. We systemically analyzed large datasets covering genomics, transcriptomics, epigenomics, metabolomics, and 34 phenotypes in over 44,000 cattle. This allowed us to provide a framework to rank over 17.7 million sequence variants based on their contribution to gene regulation, evolution, and variation in 34 complex traits. Validated in independent datasets with over 7,500 cattle, our sequence-variant ranking showed consistent performances in genomic prediction of phenotypes. Our study provides methods and an analytical framework to quantify the functional importance of sequence variants. By providing public data of biological priors on genomic markers, our work can make the global selection of animals efficient and accurate.

          Abstract

          Many genome variants shaping mammalian phenotype are hypothesized to regulate gene transcription and/or to be under selection. However, most of the evidence to support this hypothesis comes from human studies. Systematic evidence for regulatory and evolutionary signals contributing to complex traits in a different mammalian model is needed. Sequence variants associated with gene expression (expression quantitative trait loci [eQTLs]) and concentration of metabolites (metabolic quantitative trait loci [mQTLs]) and under histone-modification marks in several tissues were discovered from multiomics data of over 400 cattle. Variants under selection and evolutionary constraint were identified using genome databases of multiple species. These analyses defined 30 sets of variants, and for each set, we estimated the genetic variance the set explained across 34 complex traits in 11,923 bulls and 32,347 cows with 17,669,372 imputed variants. The per-variant trait heritability of these sets across traits was highly consistent ( r > 0.94) between bulls and cows. Based on the per-variant heritability, conserved sites across 100 vertebrate species and mQTLs ranked the highest, followed by eQTLs, young variants, those under histone-modification marks, and selection signatures. From these results, we defined a Functional-And-Evolutionary Trait Heritability (FAETH) score indicating the functionality and predicted heritability of each variant. In additional 7,551 cattle, the high FAETH-ranking variants had significantly increased genetic variances and genomic prediction accuracies in 3 production traits compared to the low FAETH-ranking variants. The FAETH framework combines the information of gene regulation, evolution, and trait heritability to rank variants, and the publicly available FAETH data provide a set of biological priors for cattle genomic selection worldwide.

          Related collections

          Most cited references43

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

          Genome-wide survey of SNP variation uncovers the genetic structure of cattle breeds.

          The imprints of domestication and breed development on the genomes of livestock likely differ from those of companion animals. A deep draft sequence assembly of shotgun reads from a single Hereford female and comparative sequences sampled from six additional breeds were used to develop probes to interrogate 37,470 single-nucleotide polymorphisms (SNPs) in 497 cattle from 19 geographically and biologically diverse breeds. These data show that cattle have undergone a rapid recent decrease in effective population size from a very large ancestral population, possibly due to bottlenecks associated with domestication, selection, and breed formation. Domestication and artificial selection appear to have left detectable signatures of selection within the cattle genome, yet the current levels of diversity within breeds are at least as great as exists within humans.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Annotation-free quantification of RNA splicing using LeafCutter

            The excision of introns from pre-mRNA is an essential step in mRNA processing. We developed LeafCutter to study sample and population variation in intron splicing. LeafCutter identifies variable splicing events from short-read RNA-seq data and finds events of high complexity. Our approach obviates the need for transcript annotations and circumvents the challenges in estimating relative isoform or exon usage in complex splicing events. LeafCutter can be used both for detecting differential splicing between sample groups, and for mapping splicing quantitative trait loci (sQTLs). Compared to contemporary methods, we find 1.4–2.1 times more sQTLs, many of which help us ascribe molecular effects to disease-associated variants. Strikingly, transcriptome-wide associations between LeafCutter intron quantifications and 40 complex traits increased the number of associated disease genes at 5% FDR by an average of 2.1-fold as compared to using gene expression levels alone. LeafCutter is fast, scalable, easy to use, and available online.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Detection of human adaptation during the past 2000 years.

              Detection of recent natural selection is a challenging problem in population genetics. Here we introduce the singleton density score (SDS), a method to infer very recent changes in allele frequencies from contemporary genome sequences. Applied to data from the UK10K Project, SDS reflects allele frequency changes in the ancestors of modern Britons during the past ~2000 to 3000 years. We see strong signals of selection at lactase and the major histocompatibility complex, and in favor of blond hair and blue eyes. For polygenic adaptation, we find that recent selection for increased height has driven allele frequency shifts across most of the genome. Moreover, we identify shifts associated with other complex traits, suggesting that polygenic adaptation has played a pervasive role in shaping genotypic and phenotypic variation in modern humans.
                Bookmark

                Author and article information

                Journal
                Proc Natl Acad Sci U S A
                Proc. Natl. Acad. Sci. U.S.A
                pnas
                pnas
                PNAS
                Proceedings of the National Academy of Sciences of the United States of America
                National Academy of Sciences
                0027-8424
                1091-6490
                24 September 2019
                9 September 2019
                9 September 2019
                : 116
                : 39
                : 19398-19408
                Affiliations
                [1] aFaculty of Veterinary & Agricultural Science, The University of Melbourne , Parkville, VIC 3052, Australia;
                [2] bAgriculture Victoria, AgriBio , Centre for AgriBiosciences, Bundoora, VIC 3083, Australia;
                [3] cCentre for Animal Science, The University of Queensland , St. Lucia, QLD 4067, Australia;
                [4] dSchool of Applied Systems Biology, La Trobe University , Bundoora, VIC 3083, Australia;
                [5] eCenter for Quantitative Genetics and Genomics, Department of Molecular Biology and Genetics, Aarhus University , DK-8830 Tjele, Denmark
                Author notes
                1To whom correspondence may be addressed. Email: ruidong.xiang@ 123456unimelb.edu.au .

                Edited by Harris A. Lewin, University of California, Davis, California, and approved August 20, 2019 (received for review March 10, 2019)

                Author contributions: R.X., I.M.M., and M.E.G. designed research; R.X., I.v.d.B., and I.M.M. performed research; R.X., I.M.M., B.J.H., C.P.P.-W., M.W., S.B., Z.L., S.J.R., C.M.R., B.A.M., C.J.V.J., H.D.D., M.S.L., and A.J.C. contributed new reagents/analytic tools; R.X., I.v.d.B., I.M.M., B.J.H., C.P.P.-W., M.W., S.B., Z.L., S.J.R., C.J.V.J., A.J.C., and M.E.G. analyzed data; and R.X. and M.E.G. wrote the paper.

                Article
                201904159
                10.1073/pnas.1904159116
                6765237
                31501319
                9e247f57-b408-482d-a68e-69f7839c63f3
                Copyright © 2019 the Author(s). Published by PNAS.

                This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND).

                History
                Page count
                Pages: 11
                Funding
                Funded by: Australian Research Council (ARC) 501100000923
                Award ID: DP160101056
                Award Recipient : Ruidong Xiang Award Recipient : Michael Goddard
                Categories
                PNAS Plus
                Biological Sciences
                Agricultural Sciences
                PNAS Plus

                gene regulation,evolution,quantitative traits,animal breeding,cattle

                Comments

                Comment on this article