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传染性法氏囊病病毒序列在大肠杆菌中表达时的内部起始和移码

Internal initiation and frameshifting in infectious bursal disease virus sequence expressed in Escherichia coli.

作者信息

Macreadie I G, Azad A A

机构信息

CSIRO, Division of Biomolecular Engineering, Parkville, Australia.

出版信息

Virology. 1991 Oct;184(2):773-6. doi: 10.1016/0042-6822(91)90450-p.

Abstract

As part of our efforts to produce native molecules of the host protective antigen (VP2) of infectious bursal disease virus (IBDV) in microorganisms, we have restored nucleotide sequences encoding the VP2 N-terminus which were not present in the original clone. In addition to this process, we produced constructs that contained +5, +4, -1, and -2 frameshifts that still allowed expression of the IBDV polyprotein, VP2 and VP3. The size of translation products and examination of the nucleotide sequence lead us to speculate that both +1 frameshifting and internal initiation events lead to the synthesis of IBDV proteins in Escherichia coli.

摘要

作为我们在微生物中生产传染性法氏囊病病毒(IBDV)宿主保护性抗原(VP2)天然分子的努力的一部分,我们恢复了原始克隆中不存在的编码VP2 N端的核苷酸序列。除了这个过程,我们还构建了包含+5、+4、-1和-2移码的构建体,这些构建体仍然允许IBDV多聚蛋白、VP2和VP3的表达。翻译产物的大小和核苷酸序列的检查使我们推测,+1移码和内部起始事件都导致了大肠杆菌中IBDV蛋白的合成。

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