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扩展莫尼茨绦虫膜联蛋白B3基因组织表达差异分析 被引量:3

Analysis of the Differential Expression of the PICKI Gene in Moniezia expansa
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摘要 【目的】探索膜联蛋白B3(Annexins B3)基因在扩展莫尼茨绦虫生长发育中的作用。【方法】研究以beta-Tubulin基因作为内参基因,采用SYBR Green real-time RT-PCR方法检测该基因在扩展莫尼茨绦虫四个不同发育阶段即头节、幼节、成节、孕节中的表达差异。【结果】标准曲线分析显示,Annexins B3和beta-Tubulin基因的Ct值与阳性质粒的浓度均呈良好的线性关系,相关系数均大于0.991,溶解曲线分析表明,产物为特异的单峰,具有较高的特异性。【结论】膜联蛋白B3基因在虫体个发育阶段中的表达丰度存在差异,从高到低依次为孕节、头节、成节、幼节。 [ Objective ] The program aimed to explore the Annexins B3 gene in the development of Moniezia expansa. [ Method ] This study developed a SYBR green real- time fluorescent quantitative PCR assay for detection of Moniezia expansa mRNA with Moniezia expansa beta - Tubulin as an interna control to construct real -time fluorescent quantitative PCR assay. [ Result ] The results showed a good linear relationships ( 〉0. 991 ) between the Ct value and the concentration of positive plasmid for each gene. The melting curve analysis showed the product was specific to a single peak, with high specificity. [ Conclusion ] Real -time PCR results showed that the expression abundance of Anrtexins B3 gene was from high to low in gravid segment, scolex, mature segment and immature segment in order.
出处 《新疆农业科学》 CAS CSCD 北大核心 2011年第10期1864-1869,共6页 Xinjiang Agricultural Sciences
基金 国家科技部"973"前期研究专项(2006CB708512) 新疆生产建设兵团杰出青年创新资金专项(2011CD005) 兰州兽医研究所家畜疫病病原生物学国家重点实验室2011年度开放基金课题(SKLVEB2011KFKT008)
关键词 ANNEXINS B3 扩展莫尼茨绦虫 RT-PCR 差异表达 Annexins B3 Moniezia expansa RT- PCR differential expression
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