Cobrinik D, Soskey L, Leis J
Department of Biochemistry, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106.
J Virol. 1988 Oct;62(10):3622-30. doi: 10.1128/JVI.62.10.3622-3630.1988.
Genetic evidence is presented which suggests the existence of an important structural element in the 5' noncoding region of avian retrovirus RNA. The proposed structure, which we term the U5-leader stem, is composed of sequences in the middle of U5 and in the leader, flanking the primer-binding site. U5 and leader mutations which would disrupt this structure caused a partial replication defect. However, nucleotide substitutions in the leader, which would structurally compensate for a U5 deletion mutation, restored normal replication. Analysis of replication intermediates of viruses with the above mutations suggests that the U5-leader stem is required for efficient DNA synthesis in vivo and for initiation of DNA synthesis from the tRNA(Trp) primer in melittin-activated virions. However, this structure does not appear to be required for binding of the tRNA(Trp) primer to viral RNA. These results support a role for the U5-leader stem structure, independent of its primary sequence, in the initiation of retroviral replication.
有遗传证据表明,禽逆转录病毒RNA的5'非编码区存在一个重要的结构元件。我们提出的结构,称之为U5-前导茎,由U5中部和前导区中位于引物结合位点两侧的序列组成。会破坏该结构的U5和前导区突变导致部分复制缺陷。然而,前导区中的核苷酸替换,在结构上可补偿U5缺失突变,恢复了正常复制。对具有上述突变的病毒复制中间体的分析表明,U5-前导茎对于体内有效的DNA合成以及从蜂毒素激活的病毒体中的tRNA(Trp)引物起始DNA合成是必需的。然而,该结构似乎不是tRNA(Trp)引物与病毒RNA结合所必需的。这些结果支持了U5-前导茎结构在逆转录病毒复制起始中具有独立于其一级序列的作用。