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三种嗜肠性小鼠冠状病毒核蛋白基因的序列分析

Sequence analysis of the nucleoprotein genes of three enterotropic strains of murine coronavirus.

作者信息

Homberger F R

机构信息

Institute of Laboratory Animal Science, University of Zurich, Switzerland.

出版信息

Arch Virol. 1995;140(3):571-9. doi: 10.1007/BF01718432.

Abstract

The nucleotide sequences of the nucleoprotein genes of three enterotropic strains of the murine coronavirus mouse hepatitis virus (MHV-Y, MHV-RI and DVIM) were determined and compared with previously reported sequences of three polytropic (respiratory) strains (MHV-A59, MHV-JHM and MHV-S). Greater than 92% homology was found among the six strains by pair-wise comparison at the nucleotide level. The genes encoded proteins of 451 to 455 residues and the deduced amino acid sequences were more than 91% homologous. A unique deletion of twelve nucleotides was found at the carboxy terminus of MHV-Y and a three nucleotide deletion was found in MHV-RI, which corresponded to the one previously reported in MHV-A59 and MHV-S. Two internal open reading frames were found within the coding region of the nucleoprotein, the smaller one was specific for the enterotropic strains. It could potentially encode a truncated version of the hypothetical protein described for MHV-A59 and MHV-S. Sequence relationship of the N gene showed no correlation with tissue tropism and no sequence or even single amino acid change unique to either tropism group was found. This indicates that the nucleoprotein of MHV probably has no part in the determination of the primary tissue tropism of an MHV strain. The role of the potential internal protein warrants further investigation.

摘要

测定了鼠冠状病毒小鼠肝炎病毒(MHV-Y、MHV-RI和DVIM)三种嗜肠性毒株核蛋白基因的核苷酸序列,并与先前报道的三种多嗜性(呼吸道)毒株(MHV-A59、MHV-JHM和MHV-S)的序列进行了比较。通过核苷酸水平的两两比较,发现这六种毒株之间的同源性大于92%。这些基因编码的蛋白质含有451至455个氨基酸残基,推导的氨基酸序列同源性超过91%。在MHV-Y的羧基末端发现了12个核苷酸的独特缺失,在MHV-RI中发现了3个核苷酸的缺失,这与先前在MHV-A59和MHV-S中报道的缺失相对应。在核蛋白的编码区内发现了两个内部开放阅读框,较小的一个对嗜肠性毒株具有特异性。它可能编码一种为MHV-A59和MHV-S所描述的假定蛋白的截短版本。N基因的序列关系与组织嗜性无关,未发现任何一个嗜性组特有的序列或甚至单个氨基酸变化。这表明MHV的核蛋白可能在MHV毒株的主要组织嗜性的决定中不起作用。潜在内部蛋白的作用值得进一步研究。

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