Moustakas A, Sonstegard T S, Hackett P B
Department of Genetics and Cell Biology, University of Minnesota, St. Paul 55108-1095.
J Virol. 1993 Jul;67(7):4350-7. doi: 10.1128/JVI.67.7.4350-4357.1993.
Three short open reading frames (ORFs) reside in the 5' leader of Rous sarcoma virus (RSV) and are conserved in all avian sarcoma-leukosis retroviruses. Both extensions of the lengths of the ORFs and alterations in their initiation codons affect viral replication and gene expression. To determine whether the effects on viral replication were due to translational regulation mediated by the ORFs, we examined translation following mutation of the initiation and termination codons of each of the three ORFs. We found that the ORFs marginally enhanced downstream gene expression. Moreover, repression of downstream gene translation was proportional to the lengths of the elongated ORFs and depended on the initiation contexts of the AUG codons. Although the ORFs play a major role in viral activities, their effects on translation were relatively minor. Rather, the ORFs may affect the fate of unspliced avian retroviral RNA in chronically infected cells by participating in the sorting of viral RNA for either translation or encapsidation into virions.
三个短开放阅读框(ORF)存在于劳氏肉瘤病毒(RSV)的5'前导序列中,并且在所有禽肉瘤-白血病逆转录病毒中都是保守的。ORF长度的延长及其起始密码子的改变都会影响病毒复制和基因表达。为了确定对病毒复制的影响是否是由于ORF介导的翻译调控所致,我们在三个ORF的每个起始和终止密码子发生突变后检测了翻译情况。我们发现这些ORF对下游基因表达有轻微增强作用。此外,下游基因翻译的抑制与延长的ORF长度成正比,并取决于AUG密码子的起始上下文。尽管这些ORF在病毒活动中起主要作用,但其对翻译的影响相对较小。相反,这些ORF可能通过参与病毒RNA的分选,使其用于翻译或包装进病毒粒子,从而影响慢性感染细胞中未剪接的禽逆转录病毒RNA的命运。