Solberg Leah C, Valdar William, Gauguier Dominique, Nunez Graciela, Taylor Amy, Burnett Stephanie, Arboledas-Hita Carmen, Hernandez-Pliego Polinka, Davidson Stuart, Burns Peter, Bhattacharya Shoumo, Hough Tertius, Higgs Douglas, Klenerman Paul, Cookson William O, Zhang Youming, Deacon Robert M, Rawlins J Nicholas P, Mott Richard, Flint Jonathan
Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford Roosevelt Drive, Oxford, OX3 7BN, UK.
Mamm Genome. 2006 Feb;17(2):129-46. doi: 10.1007/s00335-005-0112-1. Epub 2006 Feb 6.
Whole-genome genetic association studies in outbred mouse populations represent a novel approach to identifying the molecular basis of naturally occurring genetic variants, the major source of quantitative variation between inbred strains of mice. Measuring multiple phenotypes in parallel on each mouse would make the approach cost effective, but protocols for phenotyping on a large enough scale have not been developed. In this article we describe the development and deployment of a protocol to collect measures on three models of human disease (anxiety, type II diabetes, and asthma) as well as measures of mouse blood biochemistry, immunology, and hematology. We report that the protocol delivers highly significant differences among the eight inbred strains (A/J, AKR/J, BALBc/J, CBA/J, C3H/HeJ, C57BL/6 J, DBA/2 J, and LP/J), the progenitors of a genetically heterogeneous stock (HS) of mice. We report the successful collection of multiple phenotypes from 2000 outbred HS animals. The phenotypes measured in the protocol form the basis of a large-scale investigation into the genetic basis of complex traits in mice designed to examine interactions between genes and between genes and environment, as well as the main effects of genetic variants on phenotypes.
对远交小鼠群体进行全基因组遗传关联研究,是一种识别自然发生的遗传变异分子基础的新方法,而自然发生的遗传变异是小鼠近交品系间数量变异的主要来源。在每只小鼠上并行测量多种表型,会使该方法具有成本效益,但尚未开发出足够大规模的表型分析方案。在本文中,我们描述了一种方案的开发与应用,该方案用于收集三种人类疾病模型(焦虑症、II型糖尿病和哮喘)的相关指标,以及小鼠血液生物化学、免疫学和血液学指标。我们报告称,该方案在八种近交品系(A/J、AKR/J、BALBc/J、CBA/J、C3H/HeJ、C57BL/6 J、DBA/2 J和LP/J)之间产生了高度显著的差异,这八种品系是一个基因异质小鼠群体(HS)的祖系。我们报告了成功从2000只远交HS动物身上收集到多种表型。该方案中测量的表型构成了一项大规模研究的基础,该研究旨在探究小鼠复杂性状的遗传基础,以检验基因之间以及基因与环境之间的相互作用,以及遗传变异对表型的主要影响。