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广东人群8q24 rs1530300单核苷酸多态性与非综合征性唇腭裂的相关性研究

Association of a single nucleotide polymorphism in 8q24 rs1530300 and nonsyndromic cleft lip with or without cleft palate in Guangdong
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摘要 目的:探讨8q24 rs1530300单核苷酸多态性(SNP)与广东籍汉族人群非综合征性唇腭裂(NSCL/P)的相关性。方法:收集广东籍NSCL/P患儿168名及健康对照者127名的外周血,提取基因组DNA,应用高分辨率熔解曲线(HRM)技术检测rs1530300位点基因多态性,采用卡方检验进行病例组及其父母与正常对照组基因型、等位基因频率的比较分析和传递不平衡(TDT)分析。结果:成功建立8q24 rs1530300位点基因多态性检测方法。病例组及正常对照组8q24 rs1530300位点基因型频率分布均符合HardyWeinberg平衡。病例组及其父母的rs1530300位点基因型和等位基因的分布频率与正常对照组比较差异均无统计学意义(P均>0.05),等位基因也不存在传递不平衡(P>0.05)。结论:8q24 rs1530300位点多态性与中国广东人群NSCL/P无明显相关性。 OBJECTIVE: To explore the association between nonsyndromic cleft lip with or without cleft palate (NSCL/P) and genetic polymorphism of 8q24 rs1530300 in Chinese Han population located in Guangdong province. METHODS:Blood samples from 168 NSCL/P patients and 127 unrelated healthy individuals of the Chinese Guangdong population were collected. DNA was extracted and high resolution melting (HRM) was used to identify single nucleotide polymorphism of rs 1530300 in all samples. Chi square test was used to analyze the genotype and allele distribution between case group,father group,mother group and control group. Transmission-disequilibrium test was also carried out. RESULTS:The method for genotyping 8q24 rs1530300 was set up. The genotypic distribution of rs1530300 in case and control group did not deviate from the Hardy-Weinberg equilibrium. There were no significant differences in the frequency distributions of both genotypes and alleles when case group,or father group ,or mother group was compared with control group at the rs1530300 (P〉0.05). We found no evidence of allele transmission-disequilibrium at rs1530300 in cleft case-parent trios(P〉0.05). CONCLUSION:In our study,the genetic polymorphism of 8q24 rs1530300 was not associated with the development of NSCL/P in Chinese Han population located in Guangdong province.
出处 《癌变.畸变.突变》 CAS CSCD 2014年第2期131-134,139,共5页 Carcinogenesis,Teratogenesis & Mutagenesis
基金 "重生行动-全国贫困家庭唇腭裂儿童手术康复计划"项目
关键词 非综合征性唇腭裂 单核苷酸多态性 8q24rs1530300 高分辨率熔解 nonsyndromic cleft lip with or without cleft palate single nucleotide polymorphism high resolution melting
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参考文献17

  • 1Harville EW,Wilcox AJ,Lie RT,et al. Epidemiology of cleftpalate alone and cleft palate with accompanying defects[J]. Eur JEpidemiol,2007,22(6):389-395.
  • 2Dai L,Zhu J,Mao M,et al. Time trends in oral clefts inChinese newborns:data from the Chinese National BirthDefects Monitoring Network[J]. Birth Defects Res A Clin MolTeratol,2010,88(1):41-47.
  • 3SOzen MA,Suzuki K,Tolarova MM,et al. Mutation ofPVRL1 is associated with sporadic,non-syndromic cleftlip/palate in northern Venezuela[J]. Nat Genet,2001,29(2):141-142.
  • 4Vieira AR,Orioli IM,Castilla EE,et al. MSX1 and TGFB3contribute to clefting in South America[J]. J Dent Res,2003,82(4):289-292.
  • 5van den Boogaard MJ,Dorland M,Beemer FA,et al. MSX1mutation is associated with orofacial clefting and tooth agenesisin humans[J]. Nat Genet,2000,24(4):342-343.
  • 6Braybrook C,Doudney K,Mar^ano AC,et al. The T-boxtranscription factor gene TBX22 is mutated in X-linked cleftpalate and ankyloglossia[J]. Nat Genet,2001,29(2):179-183.
  • 7Riley BM,Murray JC. Sequence evaluation of FGF and FGFRgene conserved non-coding elements in non-syndromic cleft lipand palate cases[J]. Am J Med Genet A,2007,143A(24):3228-3234.
  • 8Choi SJ,Marazita ML,Hart PS,et al. The PDGF-Cregulatory region SNP rs28999109 decreases promotertranscriptional activity and is associated with CL/P[J]. Eur J HumGenet,2009,17(6):774-784.
  • 9Zucchero TM,Cooper ME,Maher BS,et al. Interferonregulatory factor 6 (IRF6) gene variants and the risk of isolatedcleft lip or palate[J]. N Engl J Med,2004,351(8):769-780.
  • 10Birnbaum S,Ludwig KU,Reutter H,et al. Key susceptibilitylocus for nonsyndromic cleft lip with or without cleft palate onchromosome 8q24[J]. Nature Genetics,2009,41(4):473-477.

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