Hunt S L, Kaminski A, Jackson R J
Department of Biochemistry, University of Cambridge, United Kingdom.
Virology. 1993 Dec;197(2):801-7. doi: 10.1006/viro.1993.1661.
Since internal initiation of translation of cardiovirus RNAs requires the approximately 450-nt segment of the viral genome immediately upstream of the authentic initiation codon for viral polyprotein synthesis, the question arises as to whether the immediately adjacent sequences, the start of the polyprotein coding region, also influence the efficiency of internal initiation. Therefore, a variety of constructs derived from encephalomyocarditis virus and Theiler's murine encephalomyelitis virus retaining various lengths of viral coding sequence were translated in rabbit reticulocyte lysates. Efficient internal initiation showed no requirement specifically for viral coding sequences, but on the other hand certain motifs, notably G-rich sequences, located immediately downstream of the initiation codon were highly inhibitory. These results suggest a possible explanation for the evolution of cardiovirus polyproteins lacking N-terminal myristylation signals and are also pertinent to the design of constructs in which the cardiovirus internal ribosome entry signal is used to drive the expression of a reporter cistron.
由于心病毒RNA的内部翻译起始需要病毒基因组中紧邻病毒多聚蛋白合成真实起始密码子上游约450个核苷酸的片段,因此就紧邻的序列(多聚蛋白编码区的起始部分)是否也影响内部起始效率这一问题便产生了。因此,在兔网织红细胞裂解物中对源自脑心肌炎病毒和泰勒氏鼠脑脊髓炎病毒的保留不同长度病毒编码序列的多种构建体进行了翻译。高效的内部起始并不特别需要病毒编码序列,但另一方面,位于起始密码子紧邻下游的某些基序,尤其是富含G的序列,具有高度抑制作用。这些结果为缺乏N端肉豆蔻酰化信号的心病毒多聚蛋白的进化提供了一种可能的解释,并且也与使用心病毒内部核糖体进入信号来驱动报告顺反子表达的构建体设计相关。