A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus

被引:95
作者
Aita, VM
Liu, JJ
Knowles, JA
Terwilliger, JD
Baltazar, R
Grunn, A
Loth, JE
Kanyas, K
Lerer, B
Endicott, J
Wang, ZY
Penchaszadeh, G
Gilliam, TC
Baron, M
机构
[1] Columbia Univ, Dept Psychiat, New York, NY 10032 USA
[2] Columbia Univ, Dept Genet & Dev, New York, NY 10032 USA
[3] Columbia Univ, Columbia Genome Ctr, New York, NY 10032 USA
[4] Hadassah Hebrew Univ, Med Ctr, Dept Psychiat, Jerusalem, Israel
关键词
D O I
10.1086/302185
中图分类号
Q3 [遗传学];
学科分类号
071007 [遗传学]; 090102 [作物遗传育种];
摘要
Previously, we demonstrated evidence of linkage to bipolar affective disorder (BP) in a single large, multigenerational family with a LOD score of 3.41 at the PFKL locus on chromosome 21q22.3. Additional families showed little support for linkage to PFKL under homogeneity or heterogeneity, in that study We I-rave expanded on that analysis, with 31 microsatellite markers at an average marker spacing of less than or equal to 2 cM, in the largest multigenerational BP pedigree series reported to date. A two-point heterogeneity (alpha=0.5) LOD score of 3.35 (P <.000156) was found at the D21S1260 locus, 5 cM proximal to PFKL. Polylocus analysis with a cluster of three neighboring markers was consistent with these results (PL-HetLOD = 3.25). In the design of this study, 373 individuals from 40 families (from a total set of 1,508 individuals in 57 families) were chosen, as a cost-effective approach to genotyping this large sample set. Linkage analyses were performed with an "affecteds-only" method. As such, our results are based solely on genetic information from affected individuals, without assumptions about the disease-locus genotypes of the unaffecteds. Furthermore, for ease of comparison, this study was performed with the same approach as a 10cM genome scan for BP loci, the results of which will be reported elsewhere.
引用
收藏
页码:210 / 217
页数:8
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