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猴病毒40(Simian virus 40)DNA中跨越主要晚期病毒信使核糖核酸大部分前导序列的片段是可有可无的。

Segments of simian virus 40 DNA spanning most of the leader sequence of the major late viral messenger RNA are dispensable.

作者信息

Subramanian K N

出版信息

Proc Natl Acad Sci U S A. 1979 Jun;76(6):2556-60. doi: 10.1073/pnas.76.6.2556.

Abstract

A highly specific procedure for the isolation of deletion mutants is described. The size and location of the deletions can be predetermined. By this method a series of deletion mutants mapping within and near the untranslated 5' leader sequence of the late 16S mRNA of simian virus 40 have been isolated. The boundaries of the deletions have been accurately determined by DNA sequence analysis. The deletions range from 20 to 223 nucleotides. All these deletions mutants are viable and grow without helper virus. The largest of these deletions removes the entire leader sequence except for six nucleotides at the 3' end that are probably involved in covalent linkage with the 5' end of the body of the mRNA located 937 nucleotides away on the genome. Three of the deletion mutants remove the 5' end of the leader that normally bears the cap structure of the mRNA. A large segment immediately preceding the leader sequence is also removed in one of these mutants, ruling out the generation of the 5' end of the mRNA via initiation of transcription at this point. The circularization of linear infecting DNA producing the DNA of the deletion mutants proceeds mainly by way of blunt end ligation in vivo.

摘要

本文描述了一种用于分离缺失突变体的高度特异性方法。缺失的大小和位置可以预先确定。通过这种方法,已经分离出一系列位于猴病毒40晚期16S mRNA非翻译5'前导序列内及附近的缺失突变体。通过DNA序列分析精确确定了缺失的边界。缺失范围为20至223个核苷酸。所有这些缺失突变体都是有活力的,并且在没有辅助病毒的情况下生长。其中最大的缺失去除了整个前导序列,除了3'端的六个核苷酸,这六个核苷酸可能参与与基因组上937个核苷酸外的mRNA主体5'端的共价连接。三个缺失突变体去除了通常带有mRNA帽结构的前导序列的5'端。在这些突变体之一中,前导序列之前的一大段也被去除,排除了通过此时转录起始产生mRNA 5'端的可能性。产生缺失突变体DNA的线性感染性DNA的环化主要通过体内平端连接进行。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/62ff/383646/b69aac464064/pnas00006-0078-a.jpg

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