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Peutz-Jeghers综合征一家系的STK11基因的突变研究
引用本文:卢泽军,崔勇,杜文辉,方巧云,周伏圣,刘建军,杨森,张学军. Peutz-Jeghers综合征一家系的STK11基因的突变研究[J]. 疾病控制杂志, 2008, 12(2): 115-117
作者姓名:卢泽军  崔勇  杜文辉  方巧云  周伏圣  刘建军  杨森  张学军
作者单位:安徽医科大学第一附属医院皮肤性病科,安徽医科大学皮肤病研究所,教育部重要遗传病基因资源利用重点实验室(省部共建),安徽,合肥,230032
基金项目:安徽省科技厅重点实验室经费资助 , 安徽省教育厅省级重点学科经费资助
摘    要:目的研究Peutz-Jeghers综合征一家系的STK11基因突变情况。方法收集1例Peutz-Jeghers综合征家系,采用聚合酶链反应(PCR)及直接测序法对该家系中4例患者STK11基因进行突变检测,以家系中的8例健康者和100例无亲缘关系的正常人作对照。结果家系中4例患者STK11基因的5号外显子第725位碱基鸟嘌呤(G)被腺嘌呤(A)替代,导致第242位的甘氨酸被谷氨酸取代(G242E),而在家系中健康者及无亲缘关系的正常人中均未发现此突变。结论错义突变c.725G>A是导致该家系临床表型的主要原因。

关 键 词:Peutz-Jeghers综合征  STK11基因  突变
文章编号:1008-6013(2008)02-0115-03
修稿时间:2008-02-26

Mutation of STK11 gene in a family with Peutz-Jeghers syndrome
LU Ze-jun,CUI Yong,DU Wen-hui,Fang Qiao-yun,ZHOU Fu-sheng,LIU Jian-jun,YANG Sen,ZHANG Xue-jun. Mutation of STK11 gene in a family with Peutz-Jeghers syndrome[J]. Chinese Journal of Disease Control and Prevention, 2008, 12(2): 115-117
Authors:LU Ze-jun  CUI Yong  DU Wen-hui  Fang Qiao-yun  ZHOU Fu-sheng  LIU Jian-jun  YANG Sen  ZHANG Xue-jun
Affiliation:LU Ze-jun; CUI Yong; DU Wen-hui; Fang Qiao-yun; ZHOU Fu-sheng; LIU Jian-jun; YANG Sen; ZHANG Xue-jun. Department of Dermatology; The First Affiliated Hospital of Anhui Medical University; Anhui Medical University; The Key Lab of Gene Resource Utilization for Genetic Diseases of Ministry of Education; Hefei 230032; China;
Abstract:Objective To explore the mutation of STK11 gene in a Chinese family with Peutz-Jeghers syndrome.Methods All the coding exons of STK11 gene were amplified by polymerase chain reaction and followed by direct sequencing.Results A missense mutation was identified which had been reported previously in the 4 patients,but normal in all controls.Conclusions The c.725G>A(p.G242E)mutation of STK11 gene is the pathologic mutation in this Chinese family.
Keywords:Peutz-Jeghers syndrome  STK11 gene  Mutation
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