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CXCR2基因多态性与奶牛体细胞评分的关联性 被引量:1

Association with CXCR2 gene polymorphism and SCS in dairy cow
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摘要 利用基因测序技术对CXCR2基因进行了多态性筛查,结果发现存在+612A→G、+684G→A、+777G→C、+855G→A、+858C→A和+861G→A等6个突变位点,其中+855为新发现的SNP。6个位点都处于连锁不平衡状态,+684与+861位点之间和+777与+858之间的相关程度高(r2分别为0.635和0.541)。基因效应模型分析表明:+855和+861位点不同基因型对奶牛体细胞评分的影响没有显著性差异(P>0.05)。+612位点不同基因型对体细胞评分的影响具有显著性差异(P<0.05),AA基因型个体的体细胞评分最低为4.19,乳房炎抗性最强。+777位点不同基因型对体细胞评分的影响差异性显著(P<0.05),GG基因型个体体细胞评分最低为4.17,对乳房炎的抗性较强,说明该基因+612和+777SNPs可作为奶牛乳房炎抗性分子标记位点。 DNA sequencing technology were used to detect the polymorphism of CXCR2 gene, results showed that, there were six polymorphism loci called+612A→G, + 684G→A, + 777G→C, +855G→A, +858C→A and +861G →A in the amplified segment,and +855 SNP was the new discovery. Linkage disequilibrium analysis results showed that the six SNPs were mutually independent in the heredity. The degree of correlation with +684 and +861, +777 and +858 were high so they can represent each other well. Linear modle analysis indicated: the two loci +855 and +861 had no significant effects on SCS(P〉0.05). Different genotypes in +612 had significant effect on SCS(P〈0.05) ,SCS LSM of AA genotype individuals had the lowest SCS 4.19 and better mastitis resistance. Different genotypes in +777 locus had significant effect on SCS(P〈0.05),SCS LSM of GG genotype was 4. 17 and had relative mastitis resistance. +612 and +777 SNPs can be used as the molecular markers for rnastitis resistance.
出处 《中国兽医学报》 CAS CSCD 北大核心 2010年第1期123-127,共5页 Chinese Journal of Veterinary Science
基金 河北省科技厅攻关资助项目(06220402D-2)
关键词 奶牛 乳房炎 体细胞评分 CXCR2基因 多态性 dairy cow mastitis SCS CXCR2 gene polymorphism
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  • 1Lewontin R. On measures of gametic disequilibrium. Genetics 1988; 120:849-52.
  • 2Chen WY, Shi YY, Zheng YL, et al. Case-control study and transmission disequilibrium test provide consistent evidence for association between schizophrenia and genetic variation in the 22q11 gene ZDHHC8. Hum Mol Genet 2004; 13:2991-5.
  • 3Shi Y, Zhao X, Yu L, et al. Genetic structure adds power to detect schizophrenia susceptibility at SLIT3 in the Chinese Han population. Genome Res 2004; 14:1345-9.
  • 4Zhao X, Shi Y, Tang J, et al. A case control and family based association study of the neuregulinl gene and schizophrenia. J Med Genet 2004; 41:31-4.
  • 5Guo S, Shi Y, Zhao X, et al. No genetic association between polymorphisms in the AMPA receptor subunit GluR4 gene (GRIA4) and schizophrenia in the Chinese population. Neurosci Lett 2004; 369:168-72.
  • 6Yang MS, Yu L, Guo TW, et al. Evidence for association between single nucleotide polymorphisms in T complex protein 1 gene and schizophrenia in the Chinese Han population. J Med Genet 2004; 41:e63.
  • 7Reich DE, Cargill M, Bolk S, et al. Linkage disequilibrium in the human genome[J]. Nature, 2001,411 (6834): 199-204.
  • 8Gabriel SB, Schaffner SF, Nguyen H, et al. The structure of haplotype blocks in the human genome[J]. Science, 2002, 296(5576) :2225 -2229.
  • 9Carlson CS, Ebede MA, Rieder M J, et al. Additional SNPs and linkage-disequilibrium analyses are necessary for whole-genome association studies in humans[J]. Nat Genet, 2003,33(4) :518-521.
  • 10Wall JD, Pritehard JK. Haplotype blocks and linkage disequilibrium in the human genome[J]. Nat Rev Genet, 2003,4(8) :587-597.

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