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高效启动逆转录所需的逆转录病毒RNA二级结构。

A retroviral RNA secondary structure required for efficient initiation of reverse transcription.

作者信息

Cobrinik D, Soskey L, Leis J

机构信息

Department of Biochemistry, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106.

出版信息

J Virol. 1988 Oct;62(10):3622-30. doi: 10.1128/JVI.62.10.3622-3630.1988.

Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1615/253503/fcda99a32f72/jvirol00089-0094-a.jpg

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