P1177
Genetic Structure of Camelus dromedarius Populations through Genome-Wide RAD Sequencing

Ciani Elena , University of Bari "Aldo Moro", Bari, Italy
Angela Doskocil , Research Institute of Wildlife Ecology, Vetmeduni, Vienna, Austria
Saitou Naruya , National Institute of Genetics, Mishima, Japan
Youcef Cherifi , Département de Génétique Moléculaire Appliquée. Université des Sciences et de la Technologie d'Oran Mohamed Boudiaf, El Mnaouer, Oran, Algeria
Asmaa Mohammed Aly Abushady , Departement of Genetics, Faculty of Agriculture, Ain Shams University, Cairo, Egypt
Habib Yahyaoui , Laboratoire Elevage et Faune Sauvage, Institut des Régions Arides, Medenine, Tunisia
Sabir Nurtazin , Department of Biodiversity and Bioresources, Al-Farabi Kazakh National University, Almaty, Kazakhstan
Pamela A. Burger , Research Institute of Wildlife Ecology, Vetmeduni, Vienna, Austria
International Camel Consortium for Genetic Improvement and Conservation , Research Institute of Wildlife Ecology, Vetmeduni, Vienna, Austria
The development of cost-effective high-throughput SNP technologies for most of our livestock species has tremendously advanced genomic research for a (sustainable) food production. Despite its worldwide relevance the dromedary (Camelus dromedarius) has been relatively left out from the livestock ”genomic revolution”, until recently with the release of two reference draft genomes assembled at scaffold level. However, no complete chromosome assembled genome and no genome-wide screening tools are yet available. We adopted a double-digest genome-wide Restriction site Associated DNA (ddRAD) sequencing approach, a method that combines traditional DNA shearing via endonucleases with the Illumina Next Generation Sequencing technology to simultaneously genotype tens to hundreds of thousands of single nucleotide polymorphism (SNP) markers in hundreds of individuals. The technology has the major advantages of not requiring substantial prior knowledge of both genome sequence and variability, while achieving per-site and per-individual costs below that of current SNP chip technology. A total of 120 animals from a wide geographic sampling area were screened with 200k genomic regions for each animal, at a theoretical coverage of 6X. From an initial set of 88K SNPs, we obtained 53K SNP genotypes after stringent filtering for a minor allele frequency (MAF) of 0.05 and locus missingness of 0.25 using PLINK. Similar to previous studies using microsatellite data on a global sample set, we could not find clear population structure, neither using STRUCTURE nor principal component analysis implemented in ADEGENET. However, we detected admixture and introgression of Bactrian camels in dromedaries from Kazakhstan and Iran. Further demographic analysis and selection tests are still on-going. This population genomic study will hopefully open the way to a larger collaborative effort for a more comprehensive characterization of the relationship between genetic and phenotypic diversity in the Camelus dromedarius species.
Handouts
  • PAG-XXV_Ciani_Burger.pdf (1.2 MB)