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AcB/BcA重组近交系小鼠:数量性状基因的表型剖析、定位与克隆策略

The AcB/BcA recombinant congenic strains of mice: strategies for phenotype dissection, mapping and cloning of quantitative trait genes.

作者信息

Fortin Anny, Diez Eduardo, Henderson Janet E, Mogil Jeffrey S, Gros Philippe, Skamene Emil

机构信息

Emerillon Therapeutics Inc., 416 de Maisonneuve West, Suite 1000, Montreal QC, Canada.

出版信息

Novartis Found Symp. 2007;281:141-53; discussion 153-5, 208-9. doi: 10.1002/9780470062128.ch12.

DOI:10.1002/9780470062128.ch12
PMID:17534071
Abstract

The AcB/BcA gene discovery platform consists of a series of 36 recombinant congenic strains (RCS) produced from the second backcross generation of the progenitor mouse strains A/J and C57BL/6J. Each individual inbred RCS carries 12.5% of the donor genome in 87.5% of the background genome. As the two parental strains are known to vary in the expression of resistance and susceptibility to a considerable number of mouse models of human diseases, the AcB/BcA RCS platform represents a valuable and versatile genetic tool to study many different phenotypes. RCS can be used to follow the segregation of single gene effects in individual strains, or to look at association/dissociation of mechanistic aspects of complex phenotypes. In addition, one can select strains with fixed alleles at known loci to look for novel gene effects, or use strains with overlapping congenic segments to delineate minimal QTL, intervals. The AcB/BcA RCS platform was used by our group and others to study a series of complex phenotypes including nociception, malaria susceptibility and lipid metabolism. Linkage mapping in secondary crosses and gene expression analysis in targeted organs allowed the identification of chromosomal regions, genes, and biological pathways which might unravel novel targets for preventive and therapeutic interventions.

摘要

AcB/BcA基因发现平台由一系列36个重组近交系(RCS)组成,这些重组近交系是由祖代小鼠品系A/J和C57BL/6J的第二次回交产生的。每个近交RCS个体在87.5%的背景基因组中携带12.5%的供体基因组。由于已知这两个亲本品系在对大量人类疾病小鼠模型的抗性和易感性表达上存在差异,AcB/BcA RCS平台是研究许多不同表型的有价值且通用的遗传工具。RCS可用于追踪单个品系中单个基因效应的分离,或观察复杂表型机制方面的关联/解离。此外,可以选择在已知位点具有固定等位基因的品系来寻找新的基因效应,或者使用具有重叠同源片段的品系来划定最小数量性状位点区间。我们小组和其他研究团队利用AcB/BcA RCS平台研究了一系列复杂表型,包括痛觉感受、疟疾易感性和脂质代谢。在二次杂交中的连锁图谱分析以及在靶向器官中的基因表达分析,使得能够鉴定出可能揭示预防和治疗干预新靶点的染色体区域、基因和生物学途径。

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