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      Origin and phylogenetic status of the local Ashanti Dwarf pig (ADP) of Ghana based on genetic analysis

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          Abstract

          Background

          The Ashanti Dwarf Pig (ADP) of Ghana is an endangered pig breed with hardy and disease resistant traits. Characterisation of animal genetic resources provides relevant data for their conservation and sustainable use for food security and economic development. We investigated the origin and phylogenetic status of the local ADP of Ghana and their crosses with modern commercial breeds based on mtDNA, MC1R, Y-chromosome sequence polymorphisms, and genome-wide SNP genotyping.

          Results

          The study involved 164 local pigs sampled from the three agro-ecological zones of Ghana. Analyses of the mitochondrial D-loop region and Y-chromosome sequences revealed both European and Asian genetic signatures, with differences between the geographical zones. Black coat colour is the most predominant within the breed, with black MC1R alleles of both Asian and European origin. European alleles for spotting are present at a low frequency in the sample set, and may account for the occurrence of spotted piglets in some APD litters. PCA analysis of SNP data revealed a strong location and breed effect on clustering of local Ghanaian pigs. On a global level, Ghanaian local pigs cluster closely with European pigs of commercial origin, but we identified intervals via F ST analyses that may elucidate loci for ADP specific traits.

          Conclusions

          The presence of both European and Asian contributions, with differences between geographical zones probably reflects trading and colonial influences. Understanding the effects of admixture on important adaptive and economic traits of the ADP and other local breeds in Africa is critical for developing sustainable conservation programmes to prevent the decline of these genetic resources.

          Electronic supplementary material

          The online version of this article (doi:10.1186/s12864-017-3536-6) contains supplementary material, which is available to authorized users.

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          Most cited references36

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          Pigmentation phenotypes of variant extension locus alleles result from point mutations that alter MSH receptor function.

          Coat colors in the chestnut horse, the yellow Labrador retriever, the red fox, and one type of yellow mouse are due to recessive alleles at the extension locus. Similarly, dominant alleles at this locus are often responsible for dark coat colors in mammals, such as the melanic form of the leopard, Panthera pardus. We show here that the murine extension locus encodes the melanocyte-stimulating hormone (MSH) receptor. In mice, the recessive yellow allele (e) results from a frameshift that produces a prematurely terminated, nonfunctioning receptor. The sombre (Eso and Eso-3J) and tobacco darkening (Etob) alleles, which both have dominant melanizing effects, results from point mutations that produce hyperactive MSH receptors. The Eso-3J receptor is constitutively activated, while the Etob receptor remains hormone responsive and produces a greater activation of its effector, adenylyl cyclase, than does the wild-type allele.
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            DNA markers reveal the complexity of livestock domestication.

            A series of recent genetic studies has revealed the remarkably complex picture of domestication in both New World and Old World livestock. By comparing mitochondrial and nuclear DNA sequences of modern breeds with their potential wild and domestic ancestors, we have gained new insights into the timing and location of domestication events that produced the farm animals of today. The real surprise has been the high number of domestication events and the diverse locations in which they took place - factors which could radically change our approach to conserving livestock biodiversity resources in the future.
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              Pattern of polymorphism after strong artificial selection in a domestication event.

              The process of strong artificial selection during a domestication event is modeled, and its effect on the pattern of DNA polymorphism is investigated. The model also considers population bottleneck during domestication. Artificial selection during domestication is different from a regular selective sweep because artificial selection acts on alleles that may have been neutral variants before domestication. Therefore, the fixation of such a beneficial allele does not always wipe out DNA variation in the surrounding region. The amount by which variation is reduced largely depends on the initial frequency of the beneficial allele, p. As a consequence, p has a strong effect on the likelihood of detecting the signature of selection during domestication from patterns of polymorphism. These theoretical results are discussed in light of data collected from maize. Although the main focus of this article is on domestication, this model can also be generalized to describe selective sweeps from standing genetic variation.
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                Author and article information

                Contributors
                roamponsah@ug.edu.gh , rich12668@yahoo.co.uk
                bms41@cam.ac.uk
                dennis30009@yahoo.com
                jb393@cam.ac.uk
                greger.larson@arch.ox.ac.uk
                na106@cam.ac.uk
                cas1001@cam.ac.uk
                Journal
                BMC Genomics
                BMC Genomics
                BMC Genomics
                BioMed Central (London )
                1471-2164
                20 February 2017
                20 February 2017
                2017
                : 18
                : 193
                Affiliations
                [1 ]ISNI 0000 0004 1937 1485, GRID grid.8652.9, Animal Breeding and Genetics Research Group, Department of Animal Science, , University of Ghana, ; P. O. Box LG 226, Legon-ACCRA, Ghana
                [2 ]ISNI 0000000121885934, GRID grid.5335.0, Mammalian Genetics Research Group, Department of Pathology, , University of Cambridge, ; Tennis Court Rd, Cambridge, CB2 1QP UK
                [3 ]Palaeogenomics and Bio-Archaeology Research Network, Research Laboratory for Archaeology, Dyson Perrins Building, South Parks Road, Oxford, OX1 3QY UK
                Article
                3536
                10.1186/s12864-017-3536-6
                5319064
                28219344
                6cce3419-fb1e-4f79-8840-6a0a4ee4b6a3
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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
                : 3 August 2016
                : 2 February 2017
                Funding
                Funded by: to Cambridge in Africa Research Excellence (CAPREx)
                Funded by: Alborada Trust (GB)
                Funded by: FundRef http://dx.doi.org/10.13039/501100000781, European Research Council;
                Award ID: 337574-UNDEAD
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100000268, Biotechnology and Biological Sciences Research Council;
                Award ID: BB/N000129/1
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2017

                Genetics
                local pigs,d-loop,gene sequencing,snp genotyping
                Genetics
                local pigs, d-loop, gene sequencing, snp genotyping

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