Morozov S Y, Miroshnichenko N A, Zelenina D A, Fedorkin O N, Solovijev A G, Lukasheva L I, Atabekov J C
AN Belozersky Laboratory of Molecular Biology and Bioorganic Chemistry, Moscow State University, USSR.
Biochimie. 1990 Sep;72(9):677-84. doi: 10.1016/0300-9084(90)90051-h.
Translation of synthetic potato virus X (PVX) RNAs was examined in Krebs II ascite cell extracts and rabbit reticulocyte lysates. Either full-length or subgenomic RNAs produced by in vitro transcription of cDNAs cloned in the T7 promoter vectors were used. Full-length PVX RNA-transcript directed the synthesis of a large polypeptide which was indistinguishable from the translation product (165 kDa) of authentic viral genomic RNA on SDS-PAGE. Translation of the full-length and 3'-truncated RNA species was stimulated by addition of m7GpppG to the T7 transcription system. Subgenomic cDNA transcripts corresponding to the 3'-proximal part of PVX RNA were efficiently translated into the PVX coat protein and 2 as yet unidentified small hydrophobic proteins.
在克雷布斯II腹水细胞提取物和兔网织红细胞裂解物中检测了合成马铃薯X病毒(PVX)RNA的翻译情况。使用的是由克隆在T7启动子载体中的cDNA经体外转录产生的全长或亚基因组RNA。全长PVX RNA转录本指导合成一种大的多肽,在SDS-PAGE上,该多肽与天然病毒基因组RNA的翻译产物(165 kDa)无法区分。向T7转录系统中添加m7GpppG可刺激全长和3'端截短的RNA种类的翻译。与PVX RNA 3'近端部分相对应的亚基因组cDNA转录本被高效翻译成PVX外壳蛋白和另外2种尚未鉴定的小疏水蛋白。