Multiple Origins and Genomic Basis of Complex Traits in Sighthounds
Li WLPapers in this archive, Liu YHPapers in this archive, Li JXPapers in this archive, Ding MTPapers in this archive, Adeola ACPapers in this archive, Isakova JPapers in this archive, Aldashev AAPapers in this archive, Peng MSPapers in this archive, Huang XPapers in this archive, Xie GPapers in this archive, Chen XPapers in this archive, Yang WKPapers in this archive, Zhou WWPapers in this archive, Ghanatsaman ZAPapers in this archive, Olaogun SCPapers in this archive, Sanke OJPapers in this archive, Dawuda PMPapers in this archive, Hytönen MKPapers in this archive, Lohi HPapers in this archive, Esmailizadeh APapers in this archive, Poyarkov ADPapers in this archive, Savolainen PPapers in this archive, Wang GDPapers in this archive, Zhang YPPapers in this archive
Abstract
Sighthounds, a distinctive group of hounds comprising numerous breeds, have their origins rooted in ancient artificial selection of dogs. In this study, we performed genome sequencing for 123 sighthounds, including one breed from Africa, six breeds from Europe, two breeds from Russia, and four breeds and 12 village dogs from the Middle East. We gathered public genome data of five sighthounds and 98 other dogs as well as 31 gray wolves to pinpoint the origin and genes influencing the morphology of the sighthound genome. Population genomic analysis suggested that sighthounds originated from native dogs independently and were comprehensively admixed among breeds, supporting the multiple origins hypothesis of sighthounds. An additional 67 published ancient wolf genomes were added for gene flow detection. Results showed dramatic admixture of ancient wolves in African sighthounds, even more than with modern wolves. Whole-genome scan analysis identified 17 positively selected genes (PSGs) in the African population, 27 PSGs in the European population, and 54 PSGs in the Middle Eastern population. None of the PSGs overlapped in the three populations. Pooled PSGs of the three populations were significantly enriched in “regulation of release of sequestered calcium ion into cytosol” (gene ontology: 0051279), which is related to blood circulation and heart contraction. In addition, ESR1, JAK2, ADRB1, PRKCE, and CAMK2D were under positive selection in all three selected groups. This suggests that different PSGs in the same pathway contributed to the similar phenotype of sighthounds. We identified an ESR1 mutation (chr1: g.42,177,149 T > C) in the transcription factor (TF) binding site of Stat5a and a JAK2 mutation (chr1: g.93,277,007 T > A) in the TF binding site of Sox5. Functional experiments confirmed that the ESR1 and JAK2 mutation reduced their expression. Our results provide new insights into the domestication history and genomic basis of sighthounds.
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