The genetic basis of breed diversification: signatures of selection in pig breeds

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The genetic basis of breed diversification: signatures of selection in pig breeds Samantha Wilkinson Lu ZH, Megens H-J, Archibald AL, Haley CS, Jackson IJ, Groenen MAM, Crooijmans RP, Ogden R, Wiener P

Breed diversification Domestication and selective breeding has produced a diversity of pig breeds What is the genetic architecture underlying this variation?

History of UK pig breeds Unique and interesting history of selective breeding 1. Selective breeding from 18 th century Breeds-crossed, selection for fat 2. Introgression from Asian breeds Growth, prolificacy, early maturing contemporary breeds formed 3. Pig breed societies set up consequence of so much crossing, some well-known breeds have undergone rapid changes; thus, according to Nathusius, the Berkshire breed of 1780 Breeds is quite kept different distinct from that of 1810 (Darwin 1868). 4. Further selection in 20 th century Reproduction, leanness, muscularity, growth Specialisation

Strong and recent genetic change Resultant UK pig breed diversity Numerous breeds Broad and distinct phenotypic diversity High breed genetic differentiation Many commercial breeds originated from UK Valuable model to study the genetic basis of phenotypic variation that arose from selection Wiener Wilkinson & Wilkinson et al. 2011. 2011. An Deciphering assessment of the individual-based genetic basis of population domestication. genetic statistical Proceedings techniques: of application the Royal to Society British B. pig Biological breeds Sciences Heredity 278:1177. 106: 261

Selection Theory: regions under selection display patterns that depart from neutral expectations

Selection mapping Measuring population genetic differentiation (F ST ) With 000s SNPs - can scan genome of populations for signatures of diversifying selection

Genetic basis of pig phenotypes Detect signatures of selection associated with pig breed diversification by mapping breed genetic differentiation QUESTIONS: 1. Do signatures of selection overlap regions already associated with phenotypic traits (QTLs and genes)? 2. What types of traits are associated with the signatures of selection? What does this tell us about the history of selective breeding and genetic characteristics underlying phenotypic diversity in pig breeds?

Porcine Data SNPs (PorcineSNP60 chip: 60,000) 13 UK/Europe breeds - 372 individuals 1 Asian breed Sequence (10x coverage, Illumina) 12 UK/Europe breeds - 52 individuals 8 Asian breeds - 24 individuals

Analysis pipeline After quality control 49,260 SNPs remained For each breed, locus-by- locus F ST estimated For each breed, moving average estimated using 13-SNP sliding window For each breed, a 99 th percentile was imposed on the F ST distribution Breed specific signatures of diversifying selection

RESULTS

Coat colour: KITLG in BERKSHIRE: black animal with 6 white points Signal of F ST : 98.36-99.01 Mb KITLG is involved in melanocyte production Investigated for role in pig colouration (Hadjiconstantouras et al. 2008; Okumura et al, 2010) Pigmentation in mice, humans

Variation at KITLG Differentiation region on SSC5 (98.0-99.0 Mb) searched for sequence variants unique to Berkshire Key variants found: 1 SNP on the 3 -UTR of KITLG in Berkshire not in other European breeds; in 1 Asian breed, the Jiangquahai 2 non-synonymous variants in KITLG in Berkshire 3/50 European and 16/24 Asian individuals, respectively Similar results by Okamura et al (2008) Jiangquahai: An Asian origin of KITLG in Berkshire MC1R implicated in Berkshire coat phenotype E P allele: 2bp insertion Interactions between the different coat loci?

Coat colour: EDNRB in GLOUCESTERSHIRE OLD SPOTS: white animal with black spots Signal of F ST : 53.5 55.5 Mb EDNRB involved in melanocyte development White coat-spotting (mice, horses)

Variation at EDNRB Residue 17 European breeds Asian breeds Genetic differentiation region on SSC11 (53.5-55.5 Mb) searched for sequence variants Leucine unique to Gloucestershire Gloucestershire Old Old Spots Spots Xiang, Jiangquahai Phenylalanine All other European breeds All other Asian breeds Key variants found: Residue 68 European breeds Asian breeds 2 non-synonymous changes in the exon of EDNRB Phenylalanine Gloucestershire Old Spots Xiang Serine All other European breeds All other Asian breeds Signal peptide N-terminal extracellular domain

Mutations at EDNRB Mutations in EDNRB lead to reduced expression or partial/complete loss-of-function Hirschsprung s disease

EDNRB and pig spotting Gloucestershire Old Spots MC1R E P allele: 2bp insertion Other European coat phenotypes also associated with E P allele At low frequency or absent in Asian breeds Xiang Jiangquahai Melanocortin Endothelin signalling Complex melanocortin-endothelin signalling in cats (Kaelin et al 2012) MC1R variant interacts with partial loss-offunction EDNRB to give Gloucestershire Old Spots its spots?

Ear phenotype variation Prick-eared breeds Intermediate-eared breeds Flat-eared breeds Berkshire Duroc British Saddleback Hampshire Landrace Gloucestershire Large White Welsh Old Spots Middle White Large Black Pietrain Tamworth Mangalica Assess genetic divergence between the different ear phenotypes: F ST : Prick-eared breeds vs flat-eared breeds Prick-eared breeds vs intermediate-eared breeds Intermediate-eared breeds vs flat-eared breeds

Signals for ear phenotype SSC5: 31.74 33.78 Mb SSC7: 31.86 34.19 Mb SSC7: 55.43 58.19 Mb SSC5: 32.28 33.80 Mb SSC7: 55.41 58.20 Mb Significant QTL on SSC7 overlaps the signal Significant QTL on SSC5 is ~10Mb upstream of the signal

Signal on SSC5 Associated with contrast between prick or intermediate ears and large flat ears Syntenic to a region in the dog genome associated with ear morphology (Boyko et al. 2010, Vaysse et al 2011)

Variation at SCC5 signal Differentiation region on SSC5 (31.0-34.0 Mb) searched for variants shared by flat-eared breeds vs prick-eared breeds: No non-synonymous differences Variants in non-protein coding sequence SNPs in regulatory elements or mirna genes may be responsible?

Selection mapping of QTLs in DUROC Fatty acid composition QTL in Duroc (Uemoto et al 2012) GWAS study found a significant SNP in this region (Yang et al 2013) Genes with a role of fatty acid synthesis found in the region: SCD (120.90-121.30 Mb) ; EVOLVL3 (123.08-123.083 Mb) Duroc has a unique meat quality composition high intramuscular fat content high concentrations of saturated and mono-unsaturated fatty acids

Conclusions Pig breeds display signatures of selection associated with highly visible phenotypic differences Gloucestershire Old Spots and Berkshire selected for distinct coat phenotypes EDNRB amino acid differences KITLG variation 3 genomic regions are associated with ear phenotype variation in pigs Influence of Asian alleles on the UK phenotypic diversity Asian breeds influenced highly visible phenotypic differences as well as production traits

Acknowledgements Study was financially supported by: UK Food Standards Agency UK Department of Environment, Food and Rural Affairs Genesis Faraday (Biosciences KTN) SPARK award BBSRC Rare Breeds Survival Trust European Research Council under the European Community s 7 th Framework Programme (FP7/2007-2013)/ERC grant #ERC-2009-AdG: 249894 (SelSweep project) Travel to EAAP 2013 financially supported by: British Society of Animal Science

Thank you... Questions? Journal article on this study: Wilkinson S, Lu ZH, Megens H-J, Archibald AL, Haley CS, Jackson IJ, Groenen MAM, Crooijmans RPMA, Ogden R, Wiener P (2013) Signatures of diversifying selection in European pig breeds. PLoS Genetics 9(4): e1003453. Current address: Scotland s Rural College The Roslin Institute Building, Easter Bush EH25 9RG, UK Email: Samantha.Wilkinson@sruc.ac.uk