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腺病毒2型纤维mRNA克隆拷贝中前导序列的核苷酸序列分析。

Nucleotide sequence analysis of the leader segments in a cloned copy of adenovirus 2 fiber mRNA.

作者信息

Zain S, Sambrook J, Roberts R J, Keller W, Fried M, Dunn A R

出版信息

Cell. 1979 Apr;16(4):851-61. doi: 10.1016/0092-8674(79)90100-4.

DOI:10.1016/0092-8674(79)90100-4
PMID:455453
Abstract

Fiber mRNA of adenovirus 2 has been used as a template for RNA-dependent DNA polymerase. The resulting cDNA/RNA hybrids have been inserted at the Pst I site of the plasmid vector pBR322 after A:T tailing. One recombinant plasmid, pJAW 43, has been characterized in detail and shown to contain sequences from the main body of fiber mRNA, the three leaders common to most late adenoviral mRNAs and a fourth leader found in some species of fiber mRNA. The complete DNA sequence of the leader region has been determined and does not contain the initiation codon AUG, although this codon does occur immediately downstream from the junction between the fourth leader and the main body of the fiber mRNA. The first leader (map coordinate 16.6) is 41 nucleotides long, the second (from 19.6) is 71 nucleotides, the third (from 26.6) is 88 nucleotides and the fourth (from 78.5) is 181 nucleotides. The location of junctions between viral leaders and intervening sequences has been determined by reference, where possible, to sequences of the adenovirus 2 genome. Although the presence of short repeated sequences at the boundaries of intervening sequences and leaders makes it impossible to locate the splice point unambiguously, all of the leader-intervening sequence junctions can be arranged to stress a common feature--the presence of the dinucleotides GT and AG at the 5' and 3' ends, respectively, of the intervening sequences. This prototype sequence, which has also been recognized at or near the splice points in other eucaryotic systems, is possibly part of a larger unit which serves as a recognition site for specific excision-ligation events that ultimately lead to the production of mature mRNAs.

摘要

腺病毒2型的纤维mRNA已被用作依赖RNA的DNA聚合酶的模板。所得的cDNA/RNA杂交体在A:T加尾后被插入质粒载体pBR322的Pst I位点。已对一种重组质粒pJAW 43进行了详细表征,结果表明它含有来自纤维mRNA主体的序列、大多数晚期腺病毒mRNA共有的三个前导序列以及在某些纤维mRNA种类中发现的第四个前导序列。已确定了前导区的完整DNA序列,该序列不包含起始密码子AUG,尽管此密码子确实位于第四个前导序列与纤维mRNA主体之间的连接处下游紧邻位置。第一个前导序列(图谱坐标16.6)长41个核苷酸,第二个(从19.6开始)长71个核苷酸,第三个(从26.6开始)长88个核苷酸,第四个(从78.5开始)长181个核苷酸。病毒前导序列与间隔序列之间连接处的位置已尽可能参照腺病毒2型基因组的序列来确定。尽管在间隔序列和前导序列的边界处存在短重复序列使得无法明确确定剪接位点,但所有前导序列-间隔序列连接处都可排列以突出一个共同特征——间隔序列的5'和3'端分别存在二核苷酸GT和AG。这种原型序列在其他真核系统的剪接位点处或其附近也已被识别,它可能是一个更大单元的一部分,该单元作为特定切除-连接事件的识别位点,最终导致成熟mRNA的产生。

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