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劳氏肉瘤病毒前导RNA的结构-功能关系

Structure-function relationship of Rous sarcoma virus leader RNA.

作者信息

Darlix J L, Zuker M, Spahr P F

出版信息

Nucleic Acids Res. 1982 Sep 11;10(17):5183-96. doi: 10.1093/nar/10.17.5183.

Abstract

Cells infected by RSV synthesize viral 35S RNA as well as subgenomic 28S and 22S RNAs coding for the Env and Src genes respectively. In addition, at least the 5' 101 nucleotides of the leader are also conserved and we have shown previously that this sequence contains a strong ribosome binding site (J.-L. Darlix et al., J. Virol. 29, 597). We now report the RNA sequence of Rous Sarcoma virus (RSV) leader RNA and propose a folding of this 5' untranslated region which brings the Cap, the initiation codon for Gag and the strong ribosome binding site close to each other. We also show that ribosomes protect a sequence just upstream from initiator Aug of Gag in vitro, and believed to interact with part of the strong ribosome binding site according to the folding proposed for the leader RNA.

摘要

被劳氏肉瘤病毒(RSV)感染的细胞会合成病毒35S RNA以及分别编码Env和Src基因的亚基因组28S和22S RNA。此外,前导序列的至少5'端101个核苷酸也是保守的,并且我们之前已经表明该序列包含一个强核糖体结合位点(J.-L. 达利克斯等人,《病毒学杂志》29卷,597页)。我们现在报告劳氏肉瘤病毒(RSV)前导RNA的RNA序列,并提出该5'非翻译区的一种折叠方式,这种折叠方式使帽结构、Gag的起始密码子和强核糖体结合位点彼此靠近。我们还表明,核糖体在体外保护Gag起始密码子AUG上游的一个序列,并且根据为前导RNA提出的折叠方式,该序列被认为与强核糖体结合位点的一部分相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0074/320864/e5ce21d845a2/nar00386-0090-a.jpg

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