首页> 美国卫生研究院文献>Nucleic Acids Research >Replication inhibition by nucleoside analogues of a recombinant Autographa californica multicapsid nuclear polyhedrosis virus harboring the herpes thymidine kinase gene driven by the IE-1(0) promoter: a new way to select recombinant baculoviruses.
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Replication inhibition by nucleoside analogues of a recombinant Autographa californica multicapsid nuclear polyhedrosis virus harboring the herpes thymidine kinase gene driven by the IE-1(0) promoter: a new way to select recombinant baculoviruses.

机译:核苷类似物对带有IE-1(0)启动子驱动的带有疱疹胸苷激酶基因的重组Autographa californica多衣壳核多角体病毒的核苷类似物的复制抑制:一种选择重组杆状病毒的新方法。

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摘要

The expression of the thymidine-thymidylate kinase (HSV1-TK), (ATP: thymidine 5'-phosphotransferase; EC 2.7.1.21) of herpes simplex virus type 1 endows the host cell with a conditional lethal phenotype which depends on the presence of nucleoside analogues metabolized by this enzyme into toxic inhibitors of DNA replication. To generate a recombinant baculovirus that could be selected against by nucleoside analogs, the HSV1-tk coding sequence was placed under the control of the Autographa californica multicapsid nuclear polyhedrosis virus (AcMNPV) immediate early promoterm IE-1(0), and this construction was introduced via homologous recombination into the polyhedrin locus of AcMNPV. Two recombinant baculoviruses harboring this gene construct at the polyhedrin locus were isolated and tested for their ability to replicate in the presence of various concentrations of the nucleoside analog 9-(1,3-Dihydroxy-2-propoxymethyl)guanine (Ganciclovir). Neither Sf9 lepidopteran cell viability nor replication of wild type or beta-Galactosidase-expressing recombinant AcMNPVs were affected by concentrations of Ganciclovir up to 100 microM. In contrast, replication of the recombinant AcMNPV virus harboring the HSV1-tk gene was inhibited by Ganciclovir in a dose-dependent manner. The inhibition was detectable at 2 microM and complete at 100 microM. This property was exploited in model isolations aimed at purifying new recombinant viruses having lost this counter-selectable gene marker as a result of homologous recombination at the polyhedrin locus after cotransfection of the viral DNA with a replacement vector. After being propagated in the presence of Ganciclovir, the progeny of such co-transfections contained over 85% recombinant viruses, demonstrating that counter-selection of parental HSV1-tk-containing viruses by Ganciclovir constitutes a novel approach for recombinant baculovirus isolation.
机译:1型单纯疱疹病毒的胸苷胸苷酸激酶(HSV1-TK)(ATP:胸苷5'-磷酸转移酶; EC 2.7.1.21)的表达使宿主细胞具有条件致命的表型,具体取决于核苷的存在通过这种酶代谢的类似物成为DNA复制的毒性抑制剂。为了产生可被核苷类似物选择的重组杆状病毒,将HSV1-tk编码序列置于加州白粉虱多衣壳核多角体病毒(AcMNPV)立即早期启动子IE-1(0)的控制之下,通过同源重组导入AcMNPV的多面体基因座。分离出在多面体基因座处具有该基因构建体的两种重组杆状病毒,并测试它们在各种浓度的核苷类似物9-(1,3-二羟基-2-丙氧基甲基)鸟嘌呤(更昔洛韦)存在下复制的能力。更昔洛韦的浓度不超过100 microM,既不影响Sf9鳞翅目细胞的存活力,也不影响野生型或表达β-半乳糖苷酶的重组AcMNPV的复制。相反,更昔洛韦以剂量依赖的方式抑制了携带HSV1-tk基因的重组AcMNPV病毒的复制。抑制在2 microM时可检测到,在100 microM时完全。该特性被用于模型分离中,该模型分离的目的是纯化新的重组病毒,该新的重组病毒是在病毒DNA与置换载体共转染后,由于多面体基因座的同源重组而失去了该可逆选择的基因标记。在更昔洛韦存在下繁殖后,此类共转染的后代包含超过85%的重组病毒,这表明更昔洛韦对含HSV1-tk的亲本病毒的反选择构成了重组杆状病毒分离的新方法。

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