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猿猴病毒40(Simian virus 40)突变体的DNA序列分析,这些突变体在病毒晚期mRNA前导区存在缺失:大小和位置相似的缺失突变体表现出不同的表型。

DNA sequence analysis of simian virus 40 mutants with deletions mapping in the leader region of the late viral mRNA's: mutants with deletions similar in size and position exhibit varied phenotypes.

作者信息

Barkan A, Mertz J E

出版信息

J Virol. 1981 Feb;37(2):730-7. doi: 10.1128/JVI.37.2.730-737.1981.

Abstract

The nucleotide sequences of 10 viable yet partially defective deletion mutants of simian virus 40 were determined. The deletions mapped within, and, in many cases, 5' to, the predominant leader sequence of the late viral mRNA's. They ranged from 74 to 187 nucleotide pairs in length. Six of the mutants had lost the sequence that corresponds to the "cap" site (5' terminus) of the most abundant class of 16S mRNA's. One of these mutants had a deletion that extended 103 nucleotide pairs into the region preceding this primary cap site and, therefore, was missing many secondary cap sites as well. A seventh mutant lacked the entire major 16S leader sequence except for the first six nucleotides at its 5' end and the last nine at its 3' end. Although these mutants differed in the size and position of their deletions, we were unable to discover any simple correlations between their growth characteristics and their DNA sequences. This finding indicates that the secondary structures of the RNA transcripts may play a more important role than the exact nucleotide sequence of the RNAs in determining how they function within the cell.

摘要

测定了猴病毒40的10个存活但部分缺陷的缺失突变体的核苷酸序列。这些缺失定位在晚期病毒mRNA的主要前导序列内部,并且在许多情况下位于其5'端。它们的长度范围为74至187个核苷酸对。其中六个突变体失去了与最丰富的一类16S mRNA的“帽”位点(5'末端)相对应的序列。这些突变体之一有一个缺失,延伸到这个主要帽位点之前的区域103个核苷酸对,因此也缺少许多二级帽位点。第七个突变体除了其5'端的前六个核苷酸和3'端的最后九个核苷酸外,缺少整个主要的16S前导序列。尽管这些突变体在缺失的大小和位置上有所不同,但我们未能发现它们生长特性与其DNA序列之间的任何简单相关性。这一发现表明,RNA转录本的二级结构在决定它们在细胞内的功能方式上可能比RNA的确切核苷酸序列起更重要的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6240/171060/aca2a0346c03/jvirol00002-0209-a.jpg

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