Papkoff J, Lai M H, Hunter T, Verma I M
Cell. 1981 Nov;27(1 Pt 2):109-19. doi: 10.1016/0092-8674(81)90365-2.
We previously showed that in vitro translation of M-MuSV virion RNA yielded a 62 kd gag gene product and an overlapping set of four proteins with approximate molecular weights of 37,000, 33,000, 24,000 and 18,000. In this paper we show, by use of hybrid arrest translation with cloned recombinant DNAs containing M-MuSV v-mosMo sequences, that the 37, 33, 24 and 18 kd proteins are synthesized in their entirety from the v-mosMo gene. Analysis of the primary sequence of these proteins shows that each one is initiated independently from AUG codons within the v-mosMo gene and utilizes the long open reading frame predicted from the v-mosMo DNA sequence. Antisera against synthetic peptides corresponding to the C terminus of the predicted v-mosMo gene product precipitate all four in vitro v-mosMo proteins.
我们先前表明,M-MuSV病毒粒子RNA的体外翻译产生了一个62kd的gag基因产物以及一组重叠的四种蛋白质,其近似分子量分别为37000、33000、24000和18000。在本文中,我们通过使用与含有M-MuSV v-mosMo序列的克隆重组DNA进行杂交阻止翻译,表明37kd、33kd、24kd和18kd的蛋白质完全由v-mosMo基因合成。对这些蛋白质一级序列的分析表明,每一种蛋白质都独立地从v-mosMo基因内的AUG密码子起始,并利用从v-mosMo DNA序列预测的长开放阅读框。针对预测的v-mosMo基因产物C末端对应的合成肽的抗血清沉淀了所有四种体外v-mosMo蛋白质。