EcoR I-P fragment has been cloned from Autographa californica multiple nuclear polyhedrosis virus (AcMNPV) genomic DNA and used as a probe. 0.5-kb and 1.1-kb fragments including p10 gene from Bombyx mori nuclear polyh...EcoR I-P fragment has been cloned from Autographa californica multiple nuclear polyhedrosis virus (AcMNPV) genomic DNA and used as a probe. 0.5-kb and 1.1-kb fragments including p10 gene from Bombyx mori nuclear polyhedrosis virus (BmNPV) have been hybridized. The p10 ORF was located in the EcoR I-R fragment. Initiation codon ATG of p 10 from BmNPV has been mutated by PCR, and the ATG region became a Bgl II site. A novel transfer vector pBmAcPV-1 has been constructed using both the p10 5’-flanking region whose initiation codon ATG has been mutated with BmNPV and the p 10 3’-flanking region of AcMNPV. The vector can recombine with not only AcMNPV DNA to express foreign gene in Sf cells, but also BmNPV DNA to express foreign gene in Bm cells. CAT gene was expressed at high level in Bm cells under the control of the mutated p10 promoter of BmNPV.展开更多
随着家蚕抗血液型脓病新品种‘华康’系列在全国的推广和应用,市面上出现了一些鱼龙混杂现象。针对这一问题,本研究用SLAF-seq(Specific-locus amplified fragment sequencing)技术对15个不同的家蚕品种(7个抗脓病品种和8个非抗脓病品种...随着家蚕抗血液型脓病新品种‘华康’系列在全国的推广和应用,市面上出现了一些鱼龙混杂现象。针对这一问题,本研究用SLAF-seq(Specific-locus amplified fragment sequencing)技术对15个不同的家蚕品种(7个抗脓病品种和8个非抗脓病品种)进行简化基因组测序,结果共获得所有检测品种的447 359个SNP位点,分析这些SNP标记在家蚕的28条染色体上的分布以及与抗脓病性能的相关性,得到第27群上的50个与抗BmNPV相关的SNP分子标记;经过PCR验证的结果与SLAF-seq测序结果一致,认为这些SNP可以作为鉴定和判别‘华康’系列品种的分子标记。展开更多
目的建立家蚕核型多角体病毒蛋白的 dot- EL ISA检测方法。方法免疫家兔制备抗蚕核型多角体病毒蛋白组份的多克隆抗体 ,并用 EL ISA间接法建立了检测方法。结果此法与人血清和兔血清无交叉反应 ,可检测微量多角体病毒蛋白 ,其灵敏度达 1...目的建立家蚕核型多角体病毒蛋白的 dot- EL ISA检测方法。方法免疫家兔制备抗蚕核型多角体病毒蛋白组份的多克隆抗体 ,并用 EL ISA间接法建立了检测方法。结果此法与人血清和兔血清无交叉反应 ,可检测微量多角体病毒蛋白 ,其灵敏度达 10 ng,且操作简便。展开更多
基金Project supported by the 8th Five-Year Plan Research Program of China.
文摘EcoR I-P fragment has been cloned from Autographa californica multiple nuclear polyhedrosis virus (AcMNPV) genomic DNA and used as a probe. 0.5-kb and 1.1-kb fragments including p10 gene from Bombyx mori nuclear polyhedrosis virus (BmNPV) have been hybridized. The p10 ORF was located in the EcoR I-R fragment. Initiation codon ATG of p 10 from BmNPV has been mutated by PCR, and the ATG region became a Bgl II site. A novel transfer vector pBmAcPV-1 has been constructed using both the p10 5’-flanking region whose initiation codon ATG has been mutated with BmNPV and the p 10 3’-flanking region of AcMNPV. The vector can recombine with not only AcMNPV DNA to express foreign gene in Sf cells, but also BmNPV DNA to express foreign gene in Bm cells. CAT gene was expressed at high level in Bm cells under the control of the mutated p10 promoter of BmNPV.
文摘随着家蚕抗血液型脓病新品种‘华康’系列在全国的推广和应用,市面上出现了一些鱼龙混杂现象。针对这一问题,本研究用SLAF-seq(Specific-locus amplified fragment sequencing)技术对15个不同的家蚕品种(7个抗脓病品种和8个非抗脓病品种)进行简化基因组测序,结果共获得所有检测品种的447 359个SNP位点,分析这些SNP标记在家蚕的28条染色体上的分布以及与抗脓病性能的相关性,得到第27群上的50个与抗BmNPV相关的SNP分子标记;经过PCR验证的结果与SLAF-seq测序结果一致,认为这些SNP可以作为鉴定和判别‘华康’系列品种的分子标记。
