Karayiorgou M, Morris M A, Morrow B, Shprintzen R J, Goldberg R, Borrow J, Gos A, Nestadt G, Wolyniec P S, Lasseter V K
Fred Hutchinson Cancer Research Center, Seattle, WA 98104, USA.
Proc Natl Acad Sci U S A. 1995 Aug 15;92(17):7612-6. doi: 10.1073/pnas.92.17.7612.
We report the results of two studies examining the genetic overlap between schizophrenia and velocardiofacial syndrome. In study A, we characterize two interstitial deletions identified on chromosome 22q11 in a sample of schizophrenic patients. The size of the deletions was estimated to be between 1.5 and 2 megabases. In study B, we examine whether variations in deletion size are associated with the schizophrenic phenotype in velocardiofacial syndrome patients. Our results show that a region of the genome that has been previously implicated by genetic linkage analysis can harbor genetic lesions that increase the susceptibility to schizophrenia. Our findings should facilitate identification and cloning of the schizophrenia susceptibility gene(s) in this region and identification of more homogeneous subgroups of patients.
我们报告了两项研究的结果,这两项研究探讨了精神分裂症与腭心面综合征之间的基因重叠情况。在研究A中,我们对一组精神分裂症患者样本中在22q11染色体上鉴定出的两个间质性缺失进行了特征描述。缺失的大小估计在1.5至2兆碱基之间。在研究B中,我们研究了缺失大小的变化是否与腭心面综合征患者的精神分裂症表型相关。我们的结果表明,先前通过基因连锁分析涉及的一个基因组区域可能存在增加精神分裂症易感性的基因损伤。我们的发现应有助于在该区域鉴定和克隆精神分裂症易感基因,并识别出更具同质性的患者亚组。