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一个精神分裂症基因座可能位于10号染色体短臂15区至11区。

A schizophrenia locus may be located in region 10p15-p11.

作者信息

Straub R E, MacLean C J, Martin R B, Ma Y, Myakishev M V, Harris-Kerr C, Webb B T, O'Neill F A, Walsh D, Kendler K S

机构信息

Department of Psychiatry, Virginia Institute for Psychiatric and Behavioral Genetics, Medical College of Virginia/Virginia Commonwealth University, Richmond 23219-1534, USA.

出版信息

Am J Med Genet. 1998 Jul 10;81(4):296-301. doi: 10.1002/(sici)1096-8628(19980710)81:4<296::aid-ajmg4>3.0.co;2-s.

Abstract

In our genomic scan of 265 Irish families with schizophrenia, we have thus far generated modest evidence for the presence of vulnerability genes in three chromosomal regions, i.e., 5q21-q31, 6p24-p22, and 8p22-p21. Outside of those regions, of all markers tested to date, D10S674 produced one of the highest pairwise heterogeneity lod (H-LOD) scores, 3.2 (P = 0.0004), when initially tested on a subset of 88 families. We then tested a total of 12 markers across a region of 32 centimorgans in region 10p15-p11 of all 265 families. The strongest evidence for linkage occurred assuming an intermediate phenotypic definition, and a recessive genetic model. The largest pairwise H-LOD score was found with marker D10S2443 (maximum 1.95, P = 0.005). Using multipoint H-LODs, we found a broad peak (maximum 1.91, P = 0.006) extending over the 11 centimorgans from marker D10S674 to marker D10S1426. Multipoint nonparametric linkage analysis produced a much broader peak, but with the maximum in the same location near D10S2443 (maximum z = 1.88, P = 0.03). Based on estimates from the multipoint analysis, this putative vulnerability locus appears to be segregating in 5-15% of the families studied, but this estimate should be viewed with caution. When evaluated in the context of our genome scan results, the evidence suggests the possibility of a fourth vulnerability locus for schizophrenia in these Irish families, in region 10p15-p11.

摘要

在我们对265个爱尔兰精神分裂症家族的基因组扫描中,到目前为止,我们已经在三个染色体区域,即5q21 - q31、6p24 - p22和8p22 - p21中获得了存在易感性基因的适度证据。在这些区域之外,在迄今为止测试的所有标记中,D10S674在最初对88个家族的子集进行测试时,产生了最高的成对异质性对数优势(H - LOD)分数之一,为3.2(P = 0.0004)。然后,我们在所有265个家族的10p15 - p11区域的32厘摩范围内总共测试了12个标记。假设采用中间表型定义和隐性遗传模型时,连锁的最强证据出现。标记D10S2443的成对H - LOD分数最高(最大值为1.95,P = 0.005)。使用多点H - LODs,我们发现了一个从标记D10S674到标记D10S1426跨越11厘摩的宽峰(最大值为1.91,P = 0.006)。多点非参数连锁分析产生了一个更宽的峰,但最大值位于靠近D10S2443的相同位置(最大值z = 1.88,P = 0.03)。基于多点分析的估计,这个假定的易感性位点似乎在5% - 15%的研究家族中分离,但这个估计应谨慎看待。在我们基因组扫描结果的背景下进行评估时,证据表明在这些爱尔兰家族的10p15 - p11区域中存在精神分裂症的第四个易感性位点的可能性。

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