High-resolution mapping of quantitative trait loci in outbred mice

被引:183
作者
Talbot, CJ
Nicod, A
Cherny, SS
Fulker, DW
Collins, AC
Flint, J [1 ]
机构
[1] John Radcliffe Hosp, Inst Mol Med, Oxford OX3 9DS, England
[2] Inst Psychiat, Social Genet & Dev & Psychiat Res Ctr, London SE5 8AF, England
[3] Univ Colorado, Inst Behav Genet, Boulder, CO 80309 USA
基金
英国惠康基金;
关键词
D O I
10.1038/6825
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Screening the whole genome of a cross between two inbred animal strains has proved to be a powerful method for detecting genetic loci underlying quantitative behavioural traits(1-7), but the level of resolution offered by quantitative trait loci (QTL) mapping is still too coarse to permit molecular cloning of the genetic determinants(8). To achieve high-resolution mapping, we used an outbred stock of mice for which the entire genealogy is known. The heterogeneous stock (HS) was established 30 years ago from an eight-way cross of C57BL/6, BALB/c, RIII, AKR, DBA/2, I, All and C3H inbred mouse strains(9). At the time of the experiment reported here, the HS mice were at generation 58, theoretically offering at least a 30-fold increase in resolution for QTL mapping compared with a backcross or an F2 intercross(10,11). Using the HS mice we have mapped a QTL influencing a psychological trait in mice to a 0.8-cM interval on chromosome 1. This method allows simultaneous fine mapping of multiple QTLs, as shown by our report of a second QTL on chromosome 12. The high resolution possible with this approach makes QTLs accessible to positional cloning.
引用
收藏
页码:305 / 308
页数:4
相关论文
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