Cao Q, Martinez M, Zhang J, Sanders A R, Badner J A, Cravchik A, Markey C J, Beshah E, Guroff J J, Maxwell M E, Kazuba D M, Whiten R, Goldin L R, Gershon E S, Gejman P V
Clinical Neurogenetics Branch, National Institute of Mental Health, Bethesda, Maryland 20892, USA.
Genomics. 1997 Jul 1;43(1):1-8. doi: 10.1006/geno.1997.4815.
We have investigated whether there is a locus on chromosome 6 that confers an increased susceptibility to schizophrenia using a two-stage approach and nonparametric linkage analysis. Allele sharing identical by descent (IBD) and multipoint maximum likelihood score (MLS) statistics were employed. Results from two tested data sets, a first data set, or genome scanning data set, and a second replication data set, show excess allele sharing for multiple markers in 6q, a chromosomal region not previously reported as linked to schizophrenia. In our genome scanning data set, excess allele sharing was found for markers on 6q13-q26. The greatest allele sharing was at interval 6q21-q22.3 at marker D6S416 (IBD percentage 69; P = 0.00024). The multipoint MLS values were greater than 2.4 in the 11.4-cM interval delimited by D6S301 and D6S303, with a maximum value of 3.06 close to D6S278 and of 3.05 at D6S454/D6S423. We did not confirm, however, the previously described linkage in 6p, when tested in the systematic genome scanning data set. The replication data set also showed excess allele sharing in chromosomal area 6q13-q26, which overlapped with the aforementioned positive linkage area of the genome scanning data set. The highest sharing of the second data set was at D6S424 (IBD percentage 64; P = 0.0004), D6S283 (IBD percentage 62; P = 0.0009), and D6S423 (IBD percentage 63; P = 0.0009). Multipoint MLS analysis yielded MLS values greater than 1 in an area of about 35 cM, which overlaps with the MLS multipoint area of linkage from the genome scanning data set. The multipoint MLS at the D6S454/D6S423 locus was 2.05. In the second data set, the maximum multipoint MLS was located about 10 cM centromeric from the maximum of the genome scanning data set, at the interval D6S424-D6S275 (2.35). Our results provide very suggestive evidence for a susceptibility locus for schizophrenia in chromosome 6q from two independent data sets.
我们采用两阶段方法和非参数连锁分析,研究了6号染色体上是否存在一个位点,该位点会增加患精神分裂症的易感性。我们使用了通过血缘相同(IBD)的等位基因共享和多点最大似然评分(MLS)统计数据。来自两个测试数据集的结果,即第一个数据集(基因组扫描数据集)和第二个复制数据集,显示在6q区域(一个先前未报道与精神分裂症相关的染色体区域)的多个标记存在过量的等位基因共享。在我们的基因组扫描数据集中,在6q13 - q26区域的标记发现了过量的等位基因共享。最大的等位基因共享发生在标记D6S416处的6q21 - q22.3区间(IBD百分比69;P = 0.00024)。在由D6S301和D6S303界定的11.4厘摩区间内,多点MLS值大于2.4,在靠近D6S278处的最大值为3.06,在D6S454/D6S423处为3.05。然而,当在系统基因组扫描数据集中进行测试时,我们并未证实先前描述的6p区域的连锁关系。复制数据集在染色体区域6q13 - q26也显示出过量的等位基因共享,该区域与基因组扫描数据集上述的阳性连锁区域重叠。第二个数据集的最高共享发生在D6S424(IBD百分比64;P = 0.0004)、D6S283(IBD百分比62;P = 0.0009)和D6S423(IBD百分比63;P = 0.0009)处。多点MLS分析在约35厘摩的区域产生了大于1的MLS值,该区域与基因组扫描数据集的连锁多点区域重叠。D6S454/D6S423位点的多点MLS为2.05。在第二个数据集中,最大的多点MLS位于距离基因组扫描数据集最大值约10厘摩着丝粒方向的D6S424 - D6S275区间(2.35)。我们的结果从两个独立数据集为6号染色体q区域存在精神分裂症易感位点提供了非常有启发性的证据。