首页 | 本学科首页   官方微博 | 高级检索  
     检索      

母系遗传耳聋家系核心成员MTO1基因的突变筛查
引用本文:耿雪侠,张立,张海军,单祥年.母系遗传耳聋家系核心成员MTO1基因的突变筛查[J].淮北煤炭师范学院学报(自然科学版),2014(1):34-37.
作者姓名:耿雪侠  张立  张海军  单祥年
作者单位:[1]淮北师范大学生命科学学院,安徽淮北235000 [2]东南大学医学院,江苏南京210009
基金项目:安徽省高校青年教师科研资助项目(2006jq1141zd);安徽省自然科学基金项目(1208085MC45);安徽省教育厅资助项目(KJ20122350)
摘    要:根据MTO1基因序列及有关文献,采用Oligo6软件设计并合成了8对引物,扩增了淮阴母系遗传非综合征耳聋大家系10例母系成员(5例听力正常,5例具有严重耳聋症状)的MTO1基因12个外显子及其与内含子交界区的DNA片段.测序结果发现5例具有严重耳聋症状患者的MTO1基因与5例听力正常个体的MTO1基因相应序列完全一致,且与MTO1标准序列相比,无任何序列变化.推测MTO1基因可能不对该家系线粒体DNA A1555G突变具有核修饰效应.

关 键 词:耳聋  家系  MTO基因  突变

Mutation Screening of MTO1 Genes of the Core Members from a Maternally Inherited Pedigree with Non-syndromic Deafness
GENG Xue-xia,ZHANG Li,ZHANG Hai-jun,SHAN Xiang-nian.Mutation Screening of MTO1 Genes of the Core Members from a Maternally Inherited Pedigree with Non-syndromic Deafness[J].Journal of Huaibei Coal Industry Teachers College(Natural Science edition),2014(1):34-37.
Authors:GENG Xue-xia  ZHANG Li  ZHANG Hai-jun  SHAN Xiang-nian
Institution:1 .School of Life Science, Huaibei University, 235000, Huaibei ,Anhui, China; 2.School of Medicine, Southeast University, 210009, Nanjing , Jiangsu , China)
Abstract:Based on the DNA sequence of human MTO1 gene and some related references,eight pairs of prim-ers were designed and used to PCR amplify the 12 exons and intron-exon junctions of MTO1 genes,from 5 affected patients and 5 unaffected matrilineal relatives with A1555G mitochondrial mutation in the Chinese extensive family with nonsyndromic deafness in Huaiyin,Jiangsu province.The sequencing result showed that no any nucleotide changes were found in MTO1 genes from 10 matrilineal members with different clinical phenotypes,which excluded the possibility that MTO1 gene may modulate the phenotypes of A1555G muta-tion in this Chinese family.
Keywords:hearing loss  pedigree  MTO1 gene  mutation
本文献已被 CNKI 维普 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号