Abstract

BackgroundDNA target enrichment by micro-array capture combined with high throughput sequencing technologies provides the possibility to obtain large amounts of sequence data (e.g. whole mitochondrial DNA genomes) from multiple individuals at relatively low costs. Previously, whole mitochondrial genome data for domestic horses (Equus caballus) were limited to only a few specimens and only short parts of the mtDNA genome (especially the hypervariable region) were investigated for larger sample sets.ResultsIn this study we investigated whole mitochondrial genomes of 59 domestic horses from 44 breeds and a single Przewalski horse (Equus przewalski) using a recently described multiplex micro-array capture approach. We found 473 variable positions within the domestic horses, 292 of which are parsimony-informative, providing a well resolved phylogenetic tree. Our divergence time estimate suggests that the mitochondrial genomes of modern horse breeds shared a common ancestor around 93,000 years ago and no later than 38,000 years ago. A Bayesian skyline plot (BSP) reveals a significant population expansion beginning 6,000-8,000 years ago with an ongoing exponential growth until the present, similar to other domestic animal species. Our data further suggest that a large sample of wild horse diversity was incorporated into the domestic population; specifically, at least 46 of the mtDNA lineages observed in domestic horses (73%) already existed before the beginning of domestication about 5,000 years ago.ConclusionsOur study provides a window into the maternal origins of extant domestic horses and confirms that modern domestic breeds present a wide sample of the mtDNA diversity found in ancestral, now extinct, wild horse populations. The data obtained allow us to detect a population expansion event coinciding with the beginning of domestication and to estimate both the minimum number of female horses incorporated into the domestic gene pool and the time depth of the domestic horse mtDNA gene pool.

Highlights

  • DNA target enrichment by micro-array capture combined with high throughput sequencing technologies provides the possibility to obtain large amounts of sequence data from multiple individuals at relatively low costs

  • 17,474 sequence reads per sample mapped to the mtDNA genome (Additional file 1, Table S2)

  • Thirteen positions (1-3, 16,121, 16,127, 16,128, 16,364, 16,371, 16,656-16,660) that show a missing base call in at least three samples were removed from the alignment

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Summary

Introduction

DNA target enrichment by micro-array capture combined with high throughput sequencing technologies provides the possibility to obtain large amounts of sequence data (e.g. whole mitochondrial DNA genomes) from multiple individuals at relatively low costs. Whole mitochondrial genome data for domestic horses (Equus caballus) were limited to only a few specimens and only short parts of the mtDNA genome (especially the hypervariable region) were investigated for larger sample sets. A number of additional studies extended the picture of horse mtDNA diversity and distribution by including additional breeds from Asia (especially from China and Mongolia) [1,2,3] and it was proposed that there is evidence of a weak phylogeographic pattern [4]. It is notable that all previous mitochondrial studies had little to no statistical support for their inferred phylogenetic trees, with most of the nodes remaining unresolved. The short sequence length and small evolutionary distance between horse breeds results in a low number of phylogenetically informative sites, and this has so far prevented high statistical support for most of the nodes within the mtDNA phylogenetic tree of the domestic horse. The phylogenetic relationships of different groups of cave bears [16] as well as of killer whales [15] were only resolved by sequencing complete mtDNA genomes

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