Quantitative trait loci affecting ethanol sensitivity in BXD recombinant inbred mice

被引:33
作者
Browman, KE [1 ]
Crabbe, JC
机构
[1] Dept Vet Affairs Med Ctr, Portland Alcohol Res Ctr R&D12, Portland, OR 97201 USA
[2] Oregon Hlth Sci Univ, Dept Behav Neurosci, Portland, OR 97201 USA
关键词
alcohol sensitivity; loss of righting reflex; ataxia; candidate genes; association;
D O I
10.1097/00000374-200001000-00003
中图分类号
R194 [卫生标准、卫生检查、医药管理];
学科分类号
摘要
Background: Genetic and environmental factors contribute to an individual's sensitivity to ethanol. although the exact genes underlying ethanol's effects are not known. Quantitative trait locus (QTL) mapping is one successful method for provisionally identifying genes participating in the mediation of a given behavior. QTL analyses seek to identify associations between a quantitative response and previously mapped marker genes across genetically diverse individuals. Many QTL analyses have been performed in BXD recombinant inbred (RI) strains of mice derived from a cross of C57BL/6J (B6) and DBA/2J (D2) progenitor strains. Methods: We conducted a QTL analysis of ethanol-induced loss of righting reflex and ataxia using a panel of 25 BXD RI strains and the progenitors B6 and D2. We measured the duration of loss of righting reflex after injection and blood ethanol concentrations upon regaining of righting reflex. Ataxia was measured as the latency to fall from a vertical screen. Results: Genome-wide QTL analyses correlating strain means with allelic status at >1500 markers identified several associations (p less than or equal to 0.01). These provisional QTLs were on all chromosomes except 2, 5, 12, 13, and X, and several map near potential candidate genes. Conclusions: These results suggest that ethanol sensitivity is determined by the actions of multiple genes and further suggest their general chromosomal map locations. These provisional linkages will now be confirmed or rejected using additional genetically segregating populations.
引用
收藏
页码:17 / 23
页数:7
相关论文
共 33 条
[1]  
Bailey D.W., 1981, MOUSE BIOMEDICAL RES, P223
[2]  
BELKNAP J, 1996, BEHAV GENET, V23, P213
[3]  
BERETTINI WH, 1994, NAT GENET, V7, P54
[4]  
BUCK K, 1999, MAMM GENOME, V9, P975
[5]  
Buck KJ, 1997, J NEUROSCI, V17, P3946
[6]   NEUROADAPTIVE RESPONSES TO CHRONIC ETHANOL [J].
BUCK, KJ ;
HARRIS, RA .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1991, 15 (03) :460-470
[7]   Quantitative trait locus analyses of sleep-times induced by sedative-hypnotics in LSXSS recombinant inbred strains of mice [J].
Christensen, SC ;
Johnson, TE ;
Markel, PD ;
Clark, VJ ;
Fulker, DW ;
Corley, RP ;
Collins, AC ;
Wehner, JM .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 1996, 20 (03) :543-550
[8]   NEUROGENETIC ADAPTIVE-MECHANISMS IN ALCOHOLISM [J].
CLONINGER, CR .
SCIENCE, 1987, 236 (4800) :410-416
[9]  
CLONINGER CR, 1981, ARCH GEN PSYCHIAT, V38, P861
[10]   A GENETIC-LINKAGE MAP OF THE MOUSE - CURRENT APPLICATIONS AND FUTURE-PROSPECTS [J].
COPELAND, NG ;
JENKINS, NA ;
GILBERT, DJ ;
EPPIG, JT ;
MALTAIS, LJ ;
MILLER, JC ;
DIETRICH, WF ;
WEAVER, A ;
LINCOLN, SE ;
STEEN, RG ;
STEIN, LD ;
NADEAU, JH ;
LANDER, ES .
SCIENCE, 1993, 262 (5130) :57-66