Gill D S, Chattopadhyay D, Banerjee A K
Proc Natl Acad Sci U S A. 1986 Dec;83(23):8873-7. doi: 10.1073/pnas.83.23.8873.
A full-length cDNA copy of the phosphoprotein (NS) mRNA of vesicular stomatitis virus (New Jersey serotype) was inserted into pGEM4 vector downstream of the promoter for bacteriophage SP6 RNA polymerase. Transcription of the cDNA in vitro resulted in the synthesis of NS mRNA, which was subsequently translated into NS protein in a cell-free rabbit reticulocyte system. The biological activity of the expressed NS protein was demonstrated by in vitro synthesis of mRNA by transcription-reconstitution with purified viral L protein and N-RNA template. Deletion mapping of the NS gene defined a specific domain between amino acid residues 213 and 247, which was essential for in vitro transcription. Removal of the COOH-terminal 21 amino acids, on the other hand, did not have a significant effect on transcription. This domain appears to be involved in efficient binding of NS protein to the N protein-RNA template.
将水疱性口炎病毒(新泽西血清型)磷蛋白(NS)mRNA的全长cDNA拷贝插入到噬菌体SP6 RNA聚合酶启动子下游的pGEM4载体中。体外对该cDNA进行转录可合成NS mRNA,随后其在无细胞兔网织红细胞系统中被翻译为NS蛋白。通过用纯化的病毒L蛋白和N-RNA模板进行转录重组体外合成mRNA,证明了所表达的NS蛋白的生物学活性。对NS基因进行缺失定位确定了氨基酸残基213至247之间的一个特定结构域,该结构域对于体外转录至关重要。另一方面,去除COOH末端的21个氨基酸对转录没有显著影响。该结构域似乎参与了NS蛋白与N蛋白-RNA模板的有效结合。