乌克兰不同牛种群体TLR1、TLR4和SLC11A1基因多态性分析

IF 0.4 Q4 AGRICULTURE, MULTIDISCIPLINARY
R. Kulibaba, Y. Liashenko, O. Ivashchenko
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引用次数: 2

摘要

的目标。通过TLR1、TLR4和SLC11A1基因多态性研究乌克兰黑白奶牛品种、乌克兰红白奶牛品种和乌克兰灰牛品种群体遗传结构的特异性。采用聚合酶链反应和限制性片段长度多态性(PCR-RFLP)方法进行研究。结果。研究结果表明,在所有实验群体中,突变8732G>A、8834G>C和2021C>T的位点TLR4为单态,而突变TLR1 (1596G>A)和突变SLC11A1 (7400C>G和7808A>T)为多态。TLR4基因8732G>A突变,只发现BB基因型个体;基因型GG的8834G>C -;通过TLR1第一外显子(1596G>A)的bcl -多态性,在每个实验群体中发现A和G等位基因变异。乌克兰黑白牛和乌克兰灰牛种群偏离Hardy-Weinberg平衡状态。在两个牛种群中,杂合子个体都有相当大的过剩(分别为31%和39%)。考虑SLC11A1基因外显子11的psti1多态性,在所有实验群体中SNP5 (7400C>G)和SNP6 (7808A>T)等位变异均为C和G, SNP6 (7808A>T)等位变异为A和T。对于SNP5 (7400C>G),所有实验组的杂合个体都有相当大的过剩(15% - 30%)。与其他品种不同,乌克兰灰牛种群中没有过量的snp6 (7808A>T)杂合子(Fis = 0,04)。结论。利用TLR1、TLR4和SLC11A1位点对乌克兰牛不同群体的遗传变异参数进行了研究。研究结果表明,由于TLR4基因的单态性,其突变位点8732G>A、8834G>C和2021C>T不可能被用于所调查牛品种的标记相关选择程序。通过对TLR1和SLC11A1位点等位基因和基因型分布的分析(在所有实验牛品种中存在不同基因型的个体)表明,在所研究牛群体的育种计划中使用这些基因的不同等位变异是可能的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Polymorphism of TLR1, TLR4, and SLC11A1 genes in populations of different cattle breeds of Ukrainian selection
Aim. To study the specificities of population genetic structure of Ukrainian Black-and-White dairy breed, Ukrainian Red-and-White dairy breed, and Ukrainian Grey cattle breed by polymorphism of TLR1, TLR4, and SLC11A1 genes. Methods. The study was conducted using the method of polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP). Results. The results of the study demonstrated that in all the experimental populations, the locus TLR4 by mutations 8732G>A, 8834G>C, and 2021C>T was monomorphic, while loci TLR1 (1596G>A) and SLC11A1 (7400C>G and 7808A>T) were polymorphic. For the TLR4 gene by 8732G>A mutation, only individu- als with genotype BB were found; by 8834G>C – with genotype GG; by 2021C>T – with genotype CC. By BclI- polymorphism in the first exon of TLR1 (1596G>A) the A and G allelic variants were found in each experimental population. The deviation from the Hardy-Weinberg equilibrium state was revealed for the populations of Ukrainian Black-and-White and Ukrainian Grey cattle breeds. A considerable excess of heterozygous individuals was fixed in both cattle populations (31 and 39 % respectively). Considering PstI-polymorphism in exon 11 of SLC11A1 gene, allelic variants C and G were found for SNP5 (7400C>G), as well as A and T for SNP6 (7808A>T) in all experimen- tal populations. As for SNP5 (7400C>G), a considerable excess (from 15 to 30 %) of heterozygous individuals was determined for all experimental groups. Unlike other breeds, there was no excess (Fis = 0,04) of heterozygotes for SNP6 (7808A>T) in the population of Ukrainian Grey cattle. Conclusions. The parameters of genetic variability in the different cattle populations of Ukrainian selection by TLR1, TLR4, and SLC11A1 loci were studied. The results of the study showed the impossibility of using TLR4 locus by 8732G>A, 8834G>C and 2021C>T mutations in the programs of marker-associated selection of the investigated cattle breeds due to its monomorphic nature. The analysis of the allele and genotype distribution by TLR1 and SLC11A1 loci (presence of individuals with different genotypes in all experimental cattle breeds) indicates the possibility of using different allelic variants of these genes in the breeding programs for the studied cattle populations.
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Agricultural Science and Practice
Agricultural Science and Practice AGRICULTURE, MULTIDISCIPLINARY-
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