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Cloned Vero cell lines transfected with full-length A-segment or ORF1 cDNA sequence of IBDV.

机译:IBDV的全长A段或ORF1 cDNA序列转染的克隆Vero细胞系。

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Recombinant plasmids containing the A-segment or VP2/4/3 gene of infectious bursal disease virus (IBDV) were transfected into Vero cells. Monoclonal Vero cell lines were generated under G418 selection. Genomic (PCR/Southern blot) and transcriptional (RT-PCR/Northern blot) analyses showed that one copy of A-segment or VP2/4/3 or a partial gene of them was randomly and stably inserted into genomic DNA of Vero cells, and was able to transcribe corresponding mRNA. IFA/IPMA and Western blot analyses further confirmed that two of the monoclonal Vero cells with insertion of the A-segment of IBDV into genomic DNA could stably express VP2, VP3 and VP5 proteins, one cell line only expressed VP2 protein, and three monoclonal Vero cell lines with genomic insertion of the VP2/4/3 gene of IBDV could express VP2, VP3 and VP4 proteins. Under G418 selection, integrated foreign genes can be inherited along with cellular genomic DNA during cell replications. Moreover, DNA fragmentation and caspase-3 activity assays illustrated that cell apoptosis did not develop in monoclonal Vero cell lines expressing VP2 and VP5 proteins. The monoclonal IBDV gene-inserted Vero cell lines developed in this study will facilitate better understanding of IBDV and other members of the Birnaviridae in an expression system that would enable investigation of virus-host cell interactions on the cellular and molecular level.
机译:将含有传染性法氏囊病病毒(IBDV)的A段或VP2 / 4/3基因的重组质粒转染到Vero细胞中。在G418选择下产生了单克隆Vero细胞系。基因组(PCR / Southern印迹)和转录(RT-PCR / Northern印迹)分析表明,A片段或VP2 / 4/3或其一部分基因的一个副本随机且稳定地插入了Vero细胞的基因组DNA中,并能够转录相应的mRNA。 IFA / IPMA和Western blot分析进一步证实,将IBDV A片段插入基因组DNA的两个单克隆Vero细胞可以稳定表达VP2,VP3和VP5蛋白,一个细胞系仅表达VP2蛋白,三个单克隆Vero细胞IBDV VP2 / 4/3基因插入了基因组的细胞株可以表达VP2,VP3和VP4蛋白。在G418选择下,整合的外源基因可以在细胞复制过程中与细胞基因组DNA一起遗传。此外,DNA片段化和caspase-3活性测定表明,在表达VP2和VP5蛋白的单克隆Vero细胞系中细胞凋亡没有发展。在这项研究中开发的插入了IBDV基因的单克隆Vero细胞系将有助于在表达系统中更好地了解IBDV和Birnaviridae的其他成员,从而可以在细胞和分子水平上研究病毒-宿主细胞的相互作用。

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