Suppr超能文献

原钙黏蛋白X/Y,一种精神分裂症和分裂情感性障碍的候选基因对:基因组序列的变性高效液相色谱分析

ProtocadherinX/Y, a candidate gene-pair for schizophrenia and schizoaffective disorder: a DHPLC investigation of genomic sequence.

作者信息

Giouzeli Maria, Williams Nic A, Lonie Lorne J, DeLisi Lynn E, Crow Timothy J

机构信息

Department of Psychiatry, POWIC SANE Research Centre, University of Oxford, Warneford Hospital, Oxford, United Kingdom.

出版信息

Am J Med Genet B Neuropsychiatr Genet. 2004 Aug 15;129B(1):1-9. doi: 10.1002/ajmg.b.30036.

Abstract

Protocadherin X and Protocadherin Y (PCDHX and PCDHY) are cell-surface adhesion molecules expressed predominantly in the brain. The PCDHX/Y gene-pair was generated by an X-Y translocation approximately 3 million years ago (MYA) that gave rise to the Homo sapiens-specific region of Xq21.3 and Yp11.2 homology. Genes within this region are expected to code for sexually dimorphic human characteristics, including, for example, cerebral asymmetry a dimension of variation that has been suggested is relevant to psychosis. We examined differences in patients with schizophrenic or schizoaffective psychosis in the genomic sequence of PCDHX and PCDHY in coding and adjacent intronic sequences using denaturing high performance liquid chromatography (DHPLC). Three coding variants were detected in PCDHX and two in PCDHY. However, neither the coding variants nor the intronic polymorphisms could be related to psychosis within families. Low sequence variation suggests selective pressure against sequence change in modern humans in contrast to the structural chromosomal and sequence changes including fixed X-Y differences that occurred in this region earlier in hominid evolution. Our findings exclude sequence variation in PCDHX/Y as relevant to the aetiology of psychosis. However, we note the unusual status of this region with respect to X-inactivation. Further investigation of the epigenetic control of PCDHX/Y in relation to psychosis is warranted.

摘要

原钙黏蛋白X和原钙黏蛋白Y(PCDHX和PCDHY)是主要在大脑中表达的细胞表面黏附分子。PCDHX/Y基因对大约在300万年前(MYA)由X-Y易位产生,该易位产生了Xq21.3和Yp11.2同源性的智人特异性区域。该区域内的基因预计编码人类性别二态性特征,例如,大脑不对称性,这一变异维度已被认为与精神病有关。我们使用变性高效液相色谱(DHPLC)检测了精神分裂症或分裂情感性精神病患者PCDHX和PCDHY编码及相邻内含子序列的基因组序列差异。在PCDHX中检测到三个编码变异,在PCDHY中检测到两个。然而,无论是编码变异还是内含子多态性都与家族内的精神病无关。低序列变异表明现代人类中存在对序列变化的选择压力,这与早期人类进化中该区域发生的包括固定的X-Y差异在内的结构染色体和序列变化形成对比。我们的研究结果排除了PCDHX/Y序列变异与精神病病因学的相关性。然而,我们注意到该区域在X染色体失活方面的特殊状态。有必要进一步研究PCDHX/Y与精神病相关的表观遗传控制。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验