Linkage analysis of extremely discordant and concordant sibling pairs identifies quantitative-trait loci that influence variation in the human personality trait neuroticism

被引:134
作者
Fullerton, J
Cubin, M
Tiwari, H
Wang, C
Bomhra, A
Davidson, S
Miller, S
Fairburn, C
Goodwin, G
Neale, MC
Fiddy, S
Mott, R
Allison, DB
Flint, J [1 ]
机构
[1] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX2 7BN, England
[2] Univ Oxford, Dept Psychiat, Oxford, England
[3] Univ Alabama, Dept Biostat, Sect Stat Genet, Birmingham, AL 35294 USA
[4] Virginia Inst Psychiat & Behav Genet, Richmond, VA USA
关键词
D O I
10.1086/374178
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Several theoretical studies have suggested that large samples of randomly ascertained siblings can be used to ascertain phenotypically extreme individuals and thereby increase power to detect genetic linkage in complex traits. Here, we report a genetic linkage scan using extremely discordant and concordant sibling pairs, selected from 34,580 sibling pairs in the southwest of England who completed a personality questionnaire. We performed a genomewide scan for quantitative-trait loci (QTLs) that influence variation in the personality trait of neuroticism, or emotional stability, and we established genomewide empirical significance thresholds by simulation. The maximum pointwise P values, expressed as the negative logarithm (base 10), were found on 1q (3.95), 4q (3.84), 7p (3.90), 12q (4.74), and 13q (3.81). These five loci met or exceeded the 5% genomewide significance threshold of 3.8 (negative logarithm of the P value). QTLs on chromosomes 1, 12, and 13 are likely to be female specific. One locus, on chromosome 1, is syntenic with that reported from QTL mapping of rodent emotionality, an animal model of neuroticism, suggesting that some animal and human QTLs influencing emotional stability may be homologous.
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收藏
页码:879 / 890
页数:12
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