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      QTLs associated with dry matter intake, metabolic mid-test weight, growth and feed efficiency have little overlap across 4 beef cattle studies

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          Abstract

          Background

          The identification of genetic markers associated with complex traits that are expensive to record such as feed intake or feed efficiency would allow these traits to be included in selection programs. To identify large-effect QTL, we performed a series of genome-wide association studies and functional analyses using 50 K and 770 K SNP genotypes scored in 5,133 animals from 4 independent beef cattle populations (Cycle VII, Angus, Hereford and Simmental × Angus) with phenotypes for average daily gain, dry matter intake, metabolic mid-test body weight and residual feed intake.

          Results

          A total of 5, 6, 11 and 10 significant QTL (defined as 1-Mb genome windows with Bonferroni-corrected P-value <0.05) were identified for average daily gain, dry matter intake, metabolic mid-test body weight and residual feed intake, respectively. The identified QTL were population-specific and had little overlap across the 4 populations. The pleiotropic or closely linked QTL on BTA 7 at 23 Mb identified in the Angus population harbours a promising candidate gene ACSL6 (acyl-CoA synthetase long-chain family member 6), and was the largest effect QTL associated with dry matter intake and mid-test body weight explaining 10.39% and 14.25% of the additive genetic variance, respectively. Pleiotropic or closely linked QTL associated with average daily gain and mid-test body weight were detected on BTA 6 at 38 Mb and BTA 7 at 93 Mb confirming previous reports. No QTL for residual feed intake explained more than 2.5% of the additive genetic variance in any population. Marker-based estimates of heritability ranged from 0.21 to 0.49 for residual feed intake across the 4 populations.

          Conclusions

          This GWAS study, which is the largest performed for feed efficiency and its component traits in beef cattle to date, identified several large-effect QTL that cumulatively explained a significant percentage of additive genetic variance within each population. Differences in the QTL identified among the different populations may be due to differences in power to detect QTL, environmental variation, or differences in the genetic architecture of trait variation among breeds. These results enhance our understanding of the biology of growth, feed intake and utilisation in beef cattle.

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              Development and Characterization of a High Density SNP Genotyping Assay for Cattle

              The success of genome-wide association (GWA) studies for the detection of sequence variation affecting complex traits in human has spurred interest in the use of large-scale high-density single nucleotide polymorphism (SNP) genotyping for the identification of quantitative trait loci (QTL) and for marker-assisted selection in model and agricultural species. A cost-effective and efficient approach for the development of a custom genotyping assay interrogating 54,001 SNP loci to support GWA applications in cattle is described. A novel algorithm for achieving a compressed inter-marker interval distribution proved remarkably successful, with median interval of 37 kb and maximum predicted gap of <350 kb. The assay was tested on a panel of 576 animals from 21 cattle breeds and six outgroup species and revealed that from 39,765 to 46,492 SNP are polymorphic within individual breeds (average minor allele frequency (MAF) ranging from 0.24 to 0.27). The assay also identified 79 putative copy number variants in cattle. Utility for GWA was demonstrated by localizing known variation for coat color and the presence/absence of horns to their correct genomic locations. The combination of SNP selection and the novel spacing algorithm allows an efficient approach for the development of high-density genotyping platforms in species having full or even moderate quality draft sequence. Aspects of the approach can be exploited in species which lack an available genome sequence. The BovineSNP50 assay described here is commercially available from Illumina and provides a robust platform for mapping disease genes and QTL in cattle.
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                Author and article information

                Contributors
                msaatchi@iastate.edu
                jbeever@illinois.edu
                deckerje@missouri.edu
                dfaulkner@email.arizona.edu
                harvey.freetly@ars.usda.gov
                slhansen@iastate.edu
                yamparah@missouri.edu
                johnsoka@wsu.edu
                steve.kachman@unl.edu
                kerleym@missouri.edu
                kijae@missouri.edu
                dloy@iastate.edu
                emarques@neogen.com
                neibergs@wsu.edu
                e.john.pollak@ars.usda.gov
                schnabelr@missouri.edu
                cseabury@cvm.tamu.edu
                dshike@illinois.edu
                warren.snelling@ars.usda.gov
                mspangler2@unlnotes.unl.edu
                bweaber@k-state.edu
                dorian@iastate.edu
                taylorjerr@missouri.edu
                Journal
                BMC Genomics
                BMC Genomics
                BMC Genomics
                BioMed Central (London )
                1471-2164
                20 November 2014
                20 November 2014
                2014
                : 15
                : 1
                : 1004
                Affiliations
                [ ]Department of Animal Science, Iowa State University, Ames, 50011 USA
                [ ]Department of Animal Sciences, University of Illinois, Urbana, 61801 USA
                [ ]Division of Animal Sciences, University of Missouri, Columbia, 65211 USA
                [ ]Department of Animal Sciences, The University of Arizona, Tucson, 85719 USA
                [ ]USDA, ARS, US Meat Animal Research Center, Clay Center, Kragujevac, 68933 USA
                [ ]Department of Animal Sciences, Washington State University, Pullman, 99164 USA
                [ ]Department of Statistics, University of Nebraska, Lincoln, 68583 USA
                [ ]GeneSeek a Neogen Company, Lincoln, 68521 USA
                [ ]Department of Veterinary Pathobiology, Texas A&M University, College Station, 77843 USA
                [ ]Department of Animal Science, University of Nebraska, Lincoln, 68583 USA
                [ ]Department of Animal Sciences and Industry, Kansas State University, Manhattan, 66506 USA
                [ ]Institute of Veterinary, Animal and Biomedical Sciences, Massey University, Palmerston North, New Zealand
                Article
                6705
                10.1186/1471-2164-15-1004
                4253998
                25410110
                a107c5b5-7512-4a64-8b6e-01defe79e943
                © Saatchi et al.; licensee BioMed Central Ltd. 2014

                This article is published under license to BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 11 March 2014
                : 31 October 2014
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2014

                Genetics
                gwas,qtl,genomic selection,feed efficiency,beef cattle
                Genetics
                gwas, qtl, genomic selection, feed efficiency, beef cattle

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