Felsenstein K M, Goff S P
Department of Biochemistry and Molecular Biophysics, Columbia University College of Physicians and Surgeons, New York, New York 10032.
J Virol. 1988 Jun;62(6):2179-82. doi: 10.1128/JVI.62.6.2179-2182.1988.
A mutant of Moloney murine leukemia virus was generated in which the UAG termination codon at the 3' end of the gag gene was changed to a CAG codon encoding glutamine. Cells carrying the mutant provirus constitutively express the gag-pol fusion protein and no detectable gag protein. The precursor is stable, is not processed by the protease domain within the precursor, and does not induce assembly and release of virion particles.
构建了莫洛尼鼠白血病病毒的一种突变体,其中gag基因3'端的UAG终止密码子被改变为编码谷氨酰胺的CAG密码子。携带突变型前病毒的细胞组成性表达gag-pol融合蛋白,未检测到gag蛋白。该前体是稳定的,不会被前体内的蛋白酶结构域加工,也不会诱导病毒粒子的组装和释放。