Effect of genetic cross on the detection of quantitative trait loci and a novel approach to mapping QTLs

被引:28
作者
Hitzemann, R
Demarest, K
Koyner, J
Cipp, L
Patel, N
Rasmussen, E
McCaughran, J
机构
[1] SUNY Stony Brook, Dept Psychiat, Stony Brook, NY 11794 USA
[2] SUNY Stony Brook, Dept Psychol, Stony Brook, NY 11794 USA
[3] SUNY Stony Brook, Dept Neurosci, Stony Brook, NY 11794 USA
[4] Vet Adm Med Ctr, Res Serv, Northport, NY 11768 USA
关键词
quantitative trait loci; mouse; ethanol; locomotor activity; haloperidol; catalepsy;
D O I
10.1016/S0091-3057(00)00421-4
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
A genome-wide scan was conducted in two Fz intercrosses, C57BL/6J (B6) x DBA/2J (D2) and BALB/cJ (C) x LP/J (LP), for three different phenotypes: basal locomotor activity, ethanol-induced locomotor activity, and haloperidol-induced catalepsy. For basal activity, significant quantitative trait loci (QTLs, LOD greater than or equal to 4.3) were detected on chromosomes 9 and 19 for the C x LP intercross and chromosome 1 for the B6 x D2 intercross. Significant QTLs for ethanol-induced activation were detected on chromosome 6 for the C x LP intercross, and on chromosomes 1 and 2 for the B6 x D2 intercross. For haloperidol-induced catalepsy, significant QTLs were detected on chromosome 14 (two different QTLs) in the C x LP intercross, and chromosomes 1 and 9 in the B6 x D2 intercross. These data illustrate the importance of the genetic cross for QTL detection. Finally, the data reported here, and elsewhere, are also used to demonstrate a novel approach to QTL detection and localization. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:767 / 772
页数:6
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