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Smith-Fineman-Myers综合征的候选基因GPC4分析
引用本文:刘奇迹,龚瑶琴,张锡宇,高贵敏,郭亦寿. Smith-Fineman-Myers综合征的候选基因GPC4分析[J]. 山东大学学报(医学版), 2004, 42(1): 29-31
作者姓名:刘奇迹  龚瑶琴  张锡宇  高贵敏  郭亦寿
作者单位:山东大学医学院医学遗传学研究所,山东,济南,250000;山东大学医学院医学遗传学研究所,山东,济南,250000;山东大学医学院医学遗传学研究所,山东,济南,250000;山东大学医学院医学遗传学研究所,山东,济南,250000;山东大学医学院医学遗传学研究所,山东,济南,250000
基金项目:973国家重大基础研究项目2001CB510303,国家杰出青年基金资助项目(30225020)
摘    要:目的:探讨GPC4基因与中国山东Smith-Fineman-Myers综合征(SFMS)的关系,并分析SFMS患者GPC4基因突变。方法:利用primer3设计扩增GPC4全部编码序列及内含子和外显子接头序列的引物,采用PCR扩增结合PCR产物直接测序方法检测GPC4基因开放性阅读框架区域基因突变。结果:在GPC4基因开放性阅读框架区域内并未检测到导致疾病的基因突变。结论:山东SFMS家系患者不是由于GPC4基因编码区域基因突变所致。

关 键 词:Smith-Fineman-Myers综合征  基因  GPC4  点突变  多基因族
文章编号:1671-7554(2004)01-0029-03
修稿时间:2003-06-24

Candidate gene analysis of Smith-Fineman-Myers syndrome
LIU Qi-ji,GONG Yao-qin,ZHANG Xi-yu,et al. Candidate gene analysis of Smith-Fineman-Myers syndrome[J]. Journal of Shandong University:Health Sciences, 2004, 42(1): 29-31
Authors:LIU Qi-ji  GONG Yao-qin  ZHANG Xi-yu  et al
Abstract:Objective: To determine the role of GPC4 in the etiology of Smith-Fineman-Myers syndrome (SFMS) from Shandong(China). Methods: All the primers used for amplifying the ORF and splice junction of GPC4 were designed by using primer3 software. The open reading frame of GPC4 was detected for mutation by PCR amplification and direct sequencing in affected males from SFMS family. Results: No disease-causing mutation was found within the open reading frame of GPC4 gene. Conclusion: The disease in SFMS family from Shandong (China) is not caused by the mutation within open reading frame of GPC4 gene.
Keywords:Smith-Fineman-Myers syndrome  Gene   GPC4  Point mutation  Multigene family
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