期刊文献+

5′HOXD基因与单纯性马蹄内翻足的相关性分析 被引量:14

Analysis of association between 5′HOXD gene and idiopathic congenital talipes equinovarus
原文传递
导出
摘要 目的检测HOXD10、HOXD12、HOXD13基因内4个已知单核苷酸多态(single nucleotide poly-morphisms,SNP)rs2593778、rs847154、rs847151、rs13392701在单纯性马蹄内翻足核心家系中的分布情况,分析各个SNP位点及所构成单倍型与单纯性马蹄内翻足的相关性。方法应用限制性片段长度多态性技术结合测序,分析84个单纯性马蹄内翻足核心家系4个SNP位点基因型;应用ETDT软件统计分析各SNP位点基因型与单纯性马蹄内翻足的相关性;应用TRANSMIT软件构建单倍型并统计分析单倍型频率是否存在差异。结果位于HOXD12基因5′侧翼序列的SNP位点rs847154和位于HOXD13第1外显子的SNP位点rs13392701在单纯性马蹄内翻核心家系中存在传递不平衡(P<0.05);位于HOXD12基因第1外显子的SNP位点rs847151未检测到多态;位于HOXD10第1外显子的SNP位点rs2593778经ETDT分析无统计学意义。结论HOXD12基因5′侧翼序列的SNP位点rs847154和位于HOXD13第1外显子的SNP位点rs13392701与单纯性先天性马蹄内翻足有明显的相关性,提示HOXD12、HOXD13可能是单纯性马蹄内翻足重要的易感基因。 Objective Four single nueleotide polymorphisms (SNP) in HOXDIO, HOXD12 and HOXD13 genes were chosen to investigate SNP and haplotypes distribution in idiopathic congenital tatipes equinovarus nuclear pedigrees. Methods Genotypes of 4 SNPs in 84 idiopathic congenital talipes equinovarus nuclear pedigrees were analyzed by restriction fragment length polymorphism and DNA sequencing. Analysis of association between SNP locus and idiopathic congenital tatipes equinovarus was performed using ETDT software. Haplotypes and their frequencies in 84 nuclear pedigrees were established and analyzed by TRANSMIT software. Results rs847151 polymorphism was not detected; the rs847154 located in 5' flanking sequence ofHOXD12 gene and the rs13392701 located in exon 1 of HOXD13 gene were noted to have transmission disequilibrium in 84 nuclear pedigrees ( P 〈 0.05 ). Contusion rs847154 located in 5' flanking sequence ofHOXD12 gene and rs13392701 located in exon 1 of HOXD13 gene are associated with idiopathic congenital tatipes equinovarus; HOXD12 and HOXD13 are important susceptible genes of idiopathic congenital tatipes equinovarus.
出处 《中华医学遗传学杂志》 CAS CSCD 北大核心 2005年第6期653-656,共4页 Chinese Journal of Medical Genetics
基金 国家重点基础研究发展规划(2001CB510301) 国家自然科学基金(30471803)~~
关键词 单纯性先天性马蹄内翻足 HOXD基因簇 单核苷酸多态 单倍型 idiopathic congenital tatipes equinovarus HOXD gene cluster single nucleotide polymorphism Implotype
  • 相关文献

参考文献13

  • 1Miedzybrodzka Z. Congenital talipes equinovarus(clubfoot):a disorder of the foot but not the hand. J Anat ,2003,202:37-42.
  • 2Lochmiller C, Johnston D, Scott A, et al. Genetic epidemiology study of ICTEV. Am J Med G enet , 1998,79:90-96.
  • 3Nelson CE, Morgan BA, et al. Analysis of HOX gene expression in the chick limb bud. Development,1996,122:1449-1466.
  • 4Wynn-Davies R. Genetic and environmental factors in the talipes equinovarus. Clin Orthop,1972,84:9-13.
  • 5Johnson RL, Tabin CJ. Molecular models for vertebrate limb development.Cell, 1997,90:979-990.
  • 6王大佳,马瑞雪,陈秋,高红,麻宏伟,吉士俊.先天性马蹄内翻足与HoxD基因传递连锁不平衡研究[J].中华小儿外科杂志,2003,24(4):348-350. 被引量:13
  • 7Favier B, Dolle P. Developmental functions of mammalian Hox genes.Mol Hum Reprod, 1997, 3:115-131.
  • 8Zakany J, Kmita M, Duboule D. A dual role for Hox genes in limb anterior-posterior asymmetry. Science,2004, 304:1669-1672.
  • 9Innis JW. Role of HOX genes in human development. Curr Opin Pediatr,1997,9:617-622.
  • 10Muragaki Y, Mundlos S, Upton J, et al. Altered growth and branching patterns in synpolydactyly caused by mutations in HOXD13. Science,1996,272: 548-550.

二级参考文献11

  • 1Dietz F. The genetics of idiopathic clubfoot. Clin Orthop. 2002,401: 39-48.
  • 2Suemori H, Noguchi S. HoxC cluster genes are dispensable for overall body plan of mouse embryonic development. Deve Biol, 2000,220: 333-342.
  • 3Spitz F, Gonzalez F, Peichel C, et al. Large scale transgenic and cluster deletion analysis of the HoxD complex separate an ancestral regulatory module from evolutionary innovations. Genes deve,2001, 15: 2209-2214.
  • 4Muragaki Y, Mundlos S, Upton J, et al. Altered growth and branching patterns in synpolydactyly eausecl by mutations in HoxD13. Science, 1996, 272: 548-551.
  • 5Mortlock DP, Innis JW. Mutation of HoxA13 in hand-foot-genital syndrome. Nat Genet, 1997, 15: 179-180.
  • 6Del CM, Jones MC, Veraksa AN, et al. Monodactylous limbs and abnormal genitalia are associated with hemizygosity for the human 2q31 region that includes the HoxD cluster. Am J Hum Genet,1999. 65:104-110.
  • 7Charite J, Graaff W, Shen S, et al. Ectopic expression of HoxB8 causes duplication of the ZPA in the Forelimb and homeric transformation of axial structures. Cell, 1994, 78: 589-601.
  • 8Mark M, Rijli FM, Chambon P. Homeobox genes in embryogenesis and pathogenesis. Pediatr Res, 1997, 42: 421-429.
  • 9Meyer A. Hox gene variation and evolution. Nature, 1998, 391:225-228.
  • 10Suemori H, Noguchi S. HoxC cluster genes are dispensable for overall body plan of mouse embryonic develolanent. Deve Biol,2000, 220: 333-342.

共引文献12

同被引文献163

引证文献14

二级引证文献31

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部