Liu Yu-Li, Shen-Jang Fann Cathy, Liu Chih-Min, Wu Jer-Yuarn, Hung Shuen-Iu, Chan Hung-Yu, Chen Jiahn-Jyh, Lin Chin-Yu, Liu Shih-Kai, Hsieh Ming H, Hwang Tzung-Jeng, Ouyang Wen-Chen, Chen Chun-Ying, Lin Jin-Jia, Chou Frank Huang-Chih, Chueh Ching-Mo, Liu Wei-Ming, Tsuang Ming-Min, Faraone Stephen V, Tsuang Ming T, Chen Wei J, Hwu Hai-Gwo
Department of Psychiatry, National Taiwan University Hospital and National Taiwan University College of Medicine, Taipei, Taiwan.
Am J Med Genet B Neuropsychiatr Genet. 2006 Jun 5;141B(4):418-20. doi: 10.1002/ajmg.b.30286.
Several studies have suggested that the regulator of G-protein signaling 4 (RGS4) may be a positional and functional candidate gene for schizophrenia. Three single nucleotide polymorphisms (SNP) located at the promoter region (SNP4 and SNP7) and the intron 1 (SNP18) of RGS4 have been verified in different ethnic groups. Positive results have been reported in these SNPs with different numbers of SNP combinatory haplotypes. In this study, these three SNP markers were genotyped in 218 schizophrenia pedigrees of Taiwan (864 individuals) for association analysis. Among these three SNPs, neither SNP4, SNP7, SNP18 has shown significant association with schizophrenia in single locus association analysis, nor any compositions of the three SNP haplotypes has shown significantly associations with the DSM-IV diagnosed schizophrenia. Our results fail to support the RGS4 as a candidate gene for schizophrenia when evaluated from these three SNP markers.
多项研究表明,G蛋白信号调节因子4(RGS4)可能是精神分裂症的一个定位和功能候选基因。位于RGS4启动子区域(SNP4和SNP7)和内含子1(SNP18)的三个单核苷酸多态性(SNP)已在不同种族群体中得到验证。在这些具有不同数量SNP组合单倍型的SNP中报告了阳性结果。在本研究中,对台湾218个精神分裂症家系(864人)中的这三个SNP标记进行基因分型以进行关联分析。在这三个SNP中,SNP4、SNP7、SNP18在单基因座关联分析中均未显示出与精神分裂症有显著关联,这三个SNP单倍型的任何组合也未显示出与DSM-IV诊断的精神分裂症有显著关联。从这三个SNP标记评估时,我们的结果不支持RGS4作为精神分裂症的候选基因。