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麻疹病毒和犬瘟热病毒的基质基因:克隆、核苷酸序列及推导的氨基酸序列。

Matrix genes of measles virus and canine distemper virus: cloning, nucleotide sequences, and deduced amino acid sequences.

作者信息

Bellini W J, Englund G, Richardson C D, Rozenblatt S, Lazzarini R A

出版信息

J Virol. 1986 May;58(2):408-16. doi: 10.1128/JVI.58.2.408-416.1986.

DOI:10.1128/JVI.58.2.408-416.1986
PMID:3754588
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC252926/
Abstract

The nucleotide sequences encoding the matrix (M) proteins of measles virus (MV) and canine distemper virus (CDV) were determined from cDNA clones containing these genes in their entirety. In both cases, single open reading frames specifying basic proteins of 335 amino acid residues were predicted from the nucleotide sequences. Both viral messages were composed of approximately 1,450 nucleotides and contained 400 nucleotides of presumptive noncoding sequences at their respective 3' ends. MV and CDV M-protein-coding regions were 67% homologous at the nucleotide level and 76% homologous at the amino acid level. Only chance homology was observed in the 400-nucleotide trailer sequences. Comparisons of the M protein sequences of MV and CDV with the sequence reported for Sendai virus (B. M. Blumberg, K. Rose, M. G. Simona, L. Roux, C. Giorgi, and D. Kolakofsky, J. Virol. 52:656-663; Y. Hidaka, T. Kanda, K. Iwasaki, A. Nomoto, T. Shioda, and H. Shibuta, Nucleic Acids Res. 12:7965-7973) indicated the greatest homology among these M proteins in the carboxyterminal third of the molecule. Secondary-structure analyses of this shared region indicated a structurally conserved, hydrophobic sequence which possibly interacted with the lipid bilayer.

摘要

从完整包含麻疹病毒(MV)和犬瘟热病毒(CDV)基质(M)蛋白基因的cDNA克隆中,确定了编码这些蛋白的核苷酸序列。在这两种情况下,根据核苷酸序列预测出单个开放阅读框,其编码由335个氨基酸残基组成的碱性蛋白。两种病毒的信使RNA均由大约1450个核苷酸组成,并且在其各自的3'末端含有400个核苷酸的推定非编码序列。MV和CDV的M蛋白编码区在核苷酸水平上同源性为67%,在氨基酸水平上同源性为76%。在400个核苷酸的尾随序列中仅观察到偶然的同源性。将MV和CDV的M蛋白序列与仙台病毒报道的序列(B.M. Blumberg、K. Rose、M.G. Simona、L. Roux、C. Giorgi和D. Kolakofsky,《病毒学杂志》52:656 - 663;Y. Hidaka、T. Kanda、K. Iwasaki、A. Nomoto、T. Shioda和H. Shibuta,《核酸研究》12:79

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