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Genome screen for platelet monoamine oxidase (MAO) activity
被引:0
|作者:
Saccone, NL
Rice, JP
Rochberg, N
Goate, A
Reich, T
Shears, S
Wu, W
Nurnberger, JI
Foroud, T
Edenberg, HJ
Li, TK
机构:
[1] Washington Univ, Sch Med, Dept Psychiat, St Louis, MO 63110 USA
[2] Indiana Univ, Dept Psychiat, Indianapolis, IN 46204 USA
[3] Indiana Univ, Dept Med & Mol Genet, Indianapolis, IN 46204 USA
[4] Indiana Univ, Dept Biochem & Mol Biol, Indianapolis, IN 46204 USA
[5] Indiana Univ, Dept Med, Indianapolis, IN 46204 USA
来源:
关键词:
MAO activity;
linkage;
quantitative trait;
sib-pair analysis;
D O I:
10.1002/(SICI)1096-8628(19991015)88:5<517::AID-AJMG15>3.0.CO;2-B
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
To identify loci involved in the control of platelet monoamine oxidase B (MAO-B) activity, a genomewide linkage screen was performed using 291 markers in 148 nuclear families containing a total of 1,008 nonindependent sib-pairs, Participants were genotyped and their platelet MAO-B activity levels were measured as part of the Collaborative Study on the Genetics of Alcoholism (COGA). Sib-pair analysis using Haseman-Elston regression was carried out with two programs, Two-point analysis on all pairs with SIBPAL indicated three markers with p-values below 0.01: D6S1018 (p=0.0004), D2S1328 (p=0.008), and D2S408 (p=0.003), MAPMAKER/SIBS multipoint analyses using independent pairs(N=409) gave maximal lod scores of 2.0 on chromosome 6 and 1.1 and 1.4 for the two regions on chromosome 2, These results are consistent with linkage, but do not provide definitive evidence. We are currently creating a denser map in these regions and have begun genotyping a second sample in COGA, (C) 1999 Wiley-Liss, Inc.
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页码:517 / 521
页数:5
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