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X染色体上与精神病和大脑不对称(相对用手技能)相关联的证据。

Evidence for linkage to psychosis and cerebral asymmetry (relative hand skill) on the X chromosome.

作者信息

Laval S H, Dann J C, Butler R J, Loftus J, Rue J, Leask S J, Bass N, Comazzi M, Vita A, Nanko S, Shaw S, Peterson P, Shields G, Smith A B, Stewart J, DeLisi L E, Crow T J

机构信息

Department of Psychiatry, Warneford Hospital, Oxford, UK.

出版信息

Am J Med Genet. 1998 Sep 7;81(5):420-7. doi: 10.1002/(sici)1096-8628(19980907)81:5<420::aid-ajmg11>3.0.co;2-e.

Abstract

The hypothesis that psychosis arises as a part of the genetic diversity associated with the evolution of language generates the prediction that illness will be linked to a gene determining cerebral asymmetry, which, from the evidence of sex chromosome aneuploidies, is present in homologous form on the X and Y chromosomes. We investigated evidence of linkage to markers on the X chromosome in 1) 178 families multiply affected with schizophrenia or schizoaffective disorder with a series of 16 markers spanning the centromere (study 1), and 2) 180 pairs of left-handed brothers with 14 markers spanning the whole chromosome (study 2). In study 1, excess allele-sharing was observed in brother-brother pairs (but not brother-sister or a small sample of sister-sister pairs) over a region of approximately 20 cM, with a maximum LOD score of 1.5 at DXS991. In study 2, an association between allele-sharing and degree of left-handedness was observed extending over approximately 60 cM, with a maximum lod score of 2.8 at DXS990 (approximately 20 cM from DXS991). Within the overlap of allele-sharing is located a block in Xq21 that transposed to the Y chromosome in recent hominid evolution and is now represented as two segments on Yp. In one of two XX males with psychosis we found that the breakpoint on the Y is located within the distal region of homology to the block in Xq21. These findings are consistent with the hypothesis that an X-Y homologous determinant of cerebral asymmetry carries the variation that contributes to the predisposition to psychotic illness.

摘要

精神病作为与语言进化相关的遗传多样性的一部分而出现的假说,产生了这样的预测:该疾病将与一个决定大脑不对称性的基因相关联,从性染色体非整倍体的证据来看,这个基因以同源形式存在于X和Y染色体上。我们调查了与X染色体上标记的连锁证据,在1)178个多重患精神分裂症或分裂情感性障碍的家系中,使用一系列跨越着丝粒的16个标记(研究1),以及2)180对左撇子兄弟,使用跨越整个染色体的14个标记(研究2)。在研究1中,在大约20厘摩的区域内,兄弟对(而非兄妹对或一小部分姐妹对)中观察到等位基因共享过量,在DXS991处最大对数优势分数为1.5。在研究2中,观察到等位基因共享与左撇子程度之间的关联延伸约60厘摩,在DXS990处最大对数优势分数为2.8(距离DXS991约20厘摩)。在等位基因共享的重叠区域内,位于Xq21的一个区段在近代人类进化过程中转移到了Y染色体上,现在在Yp上表现为两个片段。在两名患有精神病的XX男性中的一名,我们发现Y染色体上的断点位于与Xq21区段的远端同源区域内。这些发现与这样的假说一致,即大脑不对称性的X - Y同源决定因素携带了导致精神病易感性的变异。

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