期刊文献+

7个猪品种IBSP基因结构变异SV13的群体分析 被引量:1

Population analysis of structural variation SV13 in IBSP gene from seven pig breeds
原文传递
导出
摘要 应用Hiseq 2000平台测定了香猪的全基因组序列,从中发现整合素结合涎蛋白(IBSP)基因内含子4中存在结构变异,命名为SV13,为了进一步探究SV13在猪群体中的分布,采用PCR技术检测了7个猪品种的SV13基因型。7个猪品种群体中均存在DD、DA和AA三种基因型,对纯合的DD和AA基因型测序,明确D等位基因缺失了227 bp。香猪、可乐猪和糯谷猪群体以DD为优势基因型,大白猪以AA基因型为主,6个地方猪品种群体中D的基因频率明显高于大白猪品种(P<0.01),香猪和大白猪群体基因型频率处于Hardy-Weinberg不平衡状态(P<0.05)。SV13可以作为辅助鉴别6个地方猪品种和大白猪的分子标记。 A structural variation, SV13, in the intron 4 of integrin-binding sialoprotein (IBSP) gene was deduced from the resequencing results based on platform Hiseq 2000. To confirm the structural variation of SV13, the genotypes of SV13 were detected by PCR method in seven pig breeds. DD, DA and AA genotypes were all detected from seven pig breeds. The deletion of D allele was 227 bp by sequencing DD and AA genotype, respectively. The dominant genotype was DD in Xiang, Kele and Nuogu pig breeds, but it was AA in the Yorkshire pig. The frequency of D allele was significantly higher in Xiang, Kele, Nuogu, Qianbeihei, Rongchang and Jiangkou Luobo pig breeds than that in the Yorkshire pig (P〈0.01 ). In addition, the genotype frequencies of Xiang and Yorkshire pigs were in Hardy-Weinberg imbalance (P〈 0. 05). It suggested that SV13 could be taken as a molecular marker to distinguish the six indigenous pig breeds from the Yorkshire pig.
出处 《畜牧与兽医》 北大核心 2017年第4期29-32,共4页 Animal Husbandry & Veterinary Medicine
基金 国家高技术研究发展计划(863计划)(2013AA102-503) 贵州省农业攻关项目(黔科合NY[2013]3073号) 贵州大学研究生创新基金(研农2016003) 贵州省"百"层次创新型人才项目(黔科合人才2016-4012号) 国家自然科学基金(31672390)
关键词 地方猪品种 结构变异 IBSP indigenous pig breeds structural variation integrin-binding sialoprotein
  • 相关文献

参考文献5

二级参考文献77

  • 1袁凯锋,廖小梅.血友病的诊断和治疗[J].现代临床医学,2007,33(3):219-222. 被引量:11
  • 2Scherer SW, Lee C, Birney E, Altshuler DM, Eichler EE, Carter NP, Hurles ME, Feuk L. Challenges and standards in integrating surveys of structural variation. Nat Genet, 2007, 39(7 Suppl.): S7-S15.
  • 3The Human Genome Structural Variation Working Group. Completing the map of human genetic variation. A plan to identify and integrate normal structural variation into the human genome sequence. Nature, 2007, 447(10): 161-165.
  • 4Scherer SW, Osborne L. Williams-Beuren Syndrome. In: Lupski J, Stankiewicz P, eds. Genomic disorders: the genomic basis of disease. Totowa, NJ: Human Press, 2006, 221-236.
  • 5IHGSC. Initial sequencing and analysis of the human genome. Nature, 2001, 409(6822): 860-921.
  • 6Carter NP. Methods and strategies for analyzing copy number variation using DNA microarrays. Nat Genet, 2007, 39(Suppl. 7): S16-S21.
  • 7Buchanan JA, Scherer SW. Contemplating effects of genomic structural variation. Genet Med, 2008, 10(9): 639-647.
  • 8Khaja R, Zhang J, MacDonald JR, He Y, Joseph-George AM, Wei J, Rafiq MA, Qian C, Shago M, Pantano L, Aburatani H, Jones K, Redon R, Hurles M, Armengol L, Estivill X, Mural RJ, Lee C, Scherer SW, Feuk L. Genome assembly comparison identifies structural variants in the human genome. Nat Genet, 2006, 38(12): 1413-1418.
  • 9Feuk L, Carson AR, Scherer SW. Structural variation in the human genome. Nat Rev Genet, 2006, 7(2): 85-97.
  • 10Armour JAL, Palla R, Zeeuwen PLJM, den Heijer M, Schalkwijk J, Hollox EJ. Accurate, high-throughput typing of copy number variation using paralogue ratios from dispersed repeats. Nucleic Acids Res, 2007, 35(3): e19.

共引文献14

同被引文献9

引证文献1

二级引证文献5

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