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Construction and characterization of a recombinant human adenovirus vector expressing bone morphogenetic protein 2

机译:表达骨形态发生蛋白2的重组人腺病毒载体的构建与鉴定

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The aim of this study was to construct and characterize a novel recombinant human adenovirus vector expressing bone morphogenetic protein 2 (BMP2) and green fluorescent protein (GFP). The BMP2 gene in the plasmid pcDNA3-BMP2 was sequenced and the restriction enzyme recognition sites were analyzed. Following mutagenesis using polymerase chain reaction (PCR), the gene sequence after the translation termination codon was removed and new restriction sites were added. The mutated BMP2 gene (BMP2+ gene) was cloned into an adenovirus shuttle vector to obtain pShuttle cytomegalovirus (CMV)-BMP2+-internal ribosome entry site (IRES)-hrGFP-1. The adenovirus plasmid pAd CMV-BMP2+-IRES-hrGFP-1 was constructed by homologous recombination and was transfected into HEK293A cells, followed by adenovirus packaging. pAd CMV-BMP2 was used as the control. The two types of adenovirus were transfected into marrow stromal cells (MSCs). The expression of BMP2 and GFP, as well as the alkaline phosphatase (ALP) activity of expressed BMP2 were detected. Following mutagenesis, the BMP2 gene sequence and recombinant adenovirus vector were as predicted. The novel adenovirus vector expressed both BMP2 and GFP, indicating that a novel recombinant human adenovirus vector expressing BMP2 had been successfully constructed.
机译:这项研究的目的是构建和表征表达骨形态发生蛋白2(BMP2)和绿色荧光蛋白(GFP)的新型重组人腺病毒载体。对质粒pcDNA3-BMP2中的BMP2基因进行测序,并分析限制酶识别位点。使用聚合酶链反应(PCR)诱变后,去除翻译终止密码子后的基因序列,并添加新的限制性酶切位点。将突变的BMP2基因(BMP2 +基因)克隆到腺病毒穿梭载体中,获得pShuttle巨细胞病毒(CMV)-BMP2 +-内部核糖体进入位点(IRES)-hrGFP-1。通过同源重组构建腺病毒质粒pAd CMV-BMP2 + -IRES-hrGFP-1,并将其转染到HEK293A细胞中,然后包装腺病毒。将pAd CMV-BMP2用作对照。将两种类型的腺病毒转染到骨髓基质细胞(MSCs)中。检测BMP2和GFP的表达,以及表达的BMP2的碱性磷酸酶(ALP)活性。诱变后,BMP2基因序列和重组腺病毒载体如预期的那样。该新型腺病毒载体表达了BMP2和GFP,这表明已经成功构建了表达BMP2的新型重组人腺病毒载体。

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