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首页> 外文期刊>Theriogenology >A novel minisequencing single-nucleotide polymorphism marker of the lysozyme gene detects high hatchability of Tsaiya ducks (Anas platyrhynchos)
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A novel minisequencing single-nucleotide polymorphism marker of the lysozyme gene detects high hatchability of Tsaiya ducks (Anas platyrhynchos)

机译:新型的溶菌酶基因小序列单核苷酸多态性标记物可检测出高彩鸭的孵化率(Anas platyrhynchos)

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Lysozyme, one of the major albumen antimicrobials, can break down the polysaccharide walls of a broad spectrum of bacteria. This study presents a novel lysozyme marker of high hatchability in the form of minisequencing single-nucleotide polymorphisms (SNPs). Recently, lysozyme was identified by complementary DNA microarray analysis as one of several differentially expressed genes noted to influence hatchability and recognized as a marker candidate for animal marker-assisted selection. Higher levels (P < 0.05) of lysozyme mRNA (via real-time polymerase chain reaction analysis) and protein (in Western blotting results) were found to be associated with a high-hatchability phenotype. In the preliminary sequence analysis of this study, TsLy1-1 and TsLy1-2 primer pairs, designed according to the lysozyme sequence, were used to amplify small-scale genomic DNA samples from animals in two extreme groups of hatchability. Sequence analysis of the amplified 763-bp DNA products clearly showed that AA and GG genotypes of SNP g.390A > G were from the ducks of the low- and high-hatchability groups, respectively. The SNP g390A > G also created a new specificity protein 1 transcription factor binding site in the lysozyme gene. Primer pairs of TsLy2-1 and TsLy2-2 then probed the amplified 763-bp DNA products to produce a shorter fragment for easier minisequencing analysis to divide 114 ducks into GG, GA, and AA genotypes. The GG ducks had the highest hatchability, representing that a new lysozyme SNP marker of good hatchability performance can be used for the purpose of marker-assisted selection in Tsaiya ducks
机译:溶菌酶是主要的蛋白抗微生物剂之一,可分解多种细菌的多糖壁。这项研究提出了一种新型的高孵化率的溶菌酶标记物,其形式为小测序单核苷酸多态性(SNPs)。最近,溶菌酶通过互补DNA微阵列分析被鉴定为几个差异表达基因之一,这些基因被认为会影响孵化能力并被公认为是动物标记辅助选择的候选标记。发现较高水平(P <0.05)的溶菌酶mRNA(通过实时聚合酶链反应分析)和蛋白质(在蛋白质印迹结果中)与高孵化率表型有关。在这项研究的初步序列分析中,根据溶菌酶序列设计的TsLy1-1和TsLy1-2引物对被用来扩增来自两个孵化率极高的动物的小规模基因组DNA样品。扩增的763bp DNA产物的序列分析清楚地表明,SNP g.390A> G的AA和GG基因型分别来自低孵化率组和高孵化率组的鸭子。 SNP g390A> G还在溶菌酶基因中创建了一个新的特异性蛋白1转录因子结合位点。然后,TsLy2-1和TsLy2-2引物对探测到扩增的763-bp DNA产物,产生一个较短的片段,以便于进行更简单的微测序分析,从而将114只鸭子分为GG,GA和AA基因型。 GG鸭的孵化率最高,这表明可以使用一种新的具有良好孵化性能的溶菌酶SNP标记物来进行Tsaiiya鸭的标记物辅助选择

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