Saar Kathrin, Beck Alfred, Bihoreau Marie-Thérèse, Birney Ewan, Brocklebank Denise, Chen Yuan, Cuppen Edwin, Demonchy Stephanie, Dopazo Joaquin, Flicek Paul, Foglio Mario, Fujiyama Asao, Gut Ivo G, Gauguier Dominique, Guigo Roderic, Guryev Victor, Heinig Matthias, Hummel Oliver, Jahn Niels, Klages Sven, Kren Vladimir, Kube Michael, Kuhl Heiner, Kuramoto Takashi, Kuroki Yoko, Lechner Doris, Lee Young-Ae, Lopez-Bigas Nuria, Lathrop G Mark, Mashimo Tomoji, Medina Ignacio, Mott Richard, Patone Giannino, Perrier-Cornet Jeanne-Antide, Platzer Matthias, Pravenec Michal, Reinhardt Richard, Sakaki Yoshiyuki, Schilhabel Markus, Schulz Herbert, Serikawa Tadao, Shikhagaie Medya, Tatsumoto Shouji, Taudien Stefan, Toyoda Atsushi, Voigt Birger, Zelenika Diana, Zimdahl Heike, Hubner Norbert
Max-Delbrück Center for Molecular Medicine, Robert-Rossle-Strae 10, 13125 Berlin, Germany.
Nat Genet. 2008 May;40(5):560-6. doi: 10.1038/ng.124.
The laboratory rat is one of the most extensively studied model organisms. Inbred laboratory rat strains originated from limited Rattus norvegicus founder populations, and the inherited genetic variation provides an excellent resource for the correlation of genotype to phenotype. Here, we report a survey of genetic variation based on almost 3 million newly identified SNPs. We obtained accurate and complete genotypes for a subset of 20,238 SNPs across 167 distinct inbred rat strains, two rat recombinant inbred panels and an F2 intercross. Using 81% of these SNPs, we constructed high-density genetic maps, creating a large dataset of fully characterized SNPs for disease gene mapping. Our data characterize the population structure and illustrate the degree of linkage disequilibrium. We provide a detailed SNP map and demonstrate its utility for mapping of quantitative trait loci. This community resource is openly available and augments the genetic tools for this workhorse of physiological studies.
实验大鼠是研究最为广泛的模式生物之一。近交系实验大鼠品系源自数量有限的挪威大鼠奠基群体,其遗传变异为基因型与表型的关联研究提供了绝佳资源。在此,我们报告一项基于近300万个新鉴定单核苷酸多态性(SNP)的遗传变异调查。我们获得了跨越167个不同近交大鼠品系、两个大鼠重组近交系群体和一个F2杂交群体的20238个SNP子集的准确完整基因型。利用这些SNP中的81%,我们构建了高密度遗传图谱,创建了一个用于疾病基因定位的完全特征化SNP大型数据集。我们的数据表征了群体结构并说明了连锁不平衡程度。我们提供了详细的SNP图谱,并展示了其在数量性状基因座定位中的效用。这一群体资源可公开获取,增强了这一生理学研究常用模型的遗传工具。