| Literature DB >> 18971309 |
Martina Johannesson1, Regina Lopez-Aumatell, Pernilla Stridh, Margarita Diez, Jonatan Tuncel, Gloria Blázquez, Esther Martinez-Membrives, Toni Cañete, Elia Vicens-Costa, Delyth Graham, Richard R Copley, Polinka Hernandez-Pliego, Amennai D Beyeen, Johan Ockinger, Cristina Fernández-Santamaría, Percio S Gulko, Max Brenner, Adolf Tobeña, Marc Guitart-Masip, Lydia Giménez-Llort, Anna Dominiczak, Rikard Holmdahl, Dominique Gauguier, Tomas Olsson, Richard Mott, William Valdar, Eva E Redei, Alberto Fernández-Teruel, Jonathan Flint.
Abstract
The laboratory rat (Rattus norvegicus) is a key tool for the study of medicine and pharmacology for human health. A large database of phenotypes for integrated fields such as cardiovascular, neuroscience, and exercise physiology exists in the literature. However, the molecular characterization of the genetic loci that give rise to variation in these traits has proven to be difficult. Here we show how one obstacle to progress, the fine-mapping of quantitative trait loci (QTL), can be overcome by using an outbred population of rats. By use of a genetically heterogeneous stock of rats, we map a locus contributing to variation in a fear-related measure (two-way active avoidance in the shuttle box) to a region on chromosome 5 containing nine genes. By establishing a protocol measuring multiple phenotypes including immunology, neuroinflammation, and hematology, as well as cardiovascular, metabolic, and behavioral traits, we establish the rat HS as a new resource for the fine-mapping of QTLs contributing to variation in complex traits of biomedical relevance.Entities:
Mesh:
Year: 2008 PMID: 18971309 PMCID: PMC2612958 DOI: 10.1101/gr.081497.108
Source DB: PubMed Journal: Genome Res ISSN: 1088-9051 Impact factor: 9.043