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一株英国猪呼吸道冠状病毒分离株病毒粒子蛋白基因的克隆与测序:与传染性胃肠炎病毒基因的比较

The cloning and sequencing of the virion protein genes from a British isolate of porcine respiratory coronavirus: comparison with transmissible gastroenteritis virus genes.

作者信息

Britton P, Mawditt K L, Page K W

机构信息

Division of Molecular Biology A.F.R.C., Institute for Animal Health, Compton, U.K.

出版信息

Virus Res. 1991 Nov;21(3):181-98. doi: 10.1016/0168-1702(91)90032-q.

Abstract

Previous analysis of porcine respiratory coronavirus (PRCV) mRNA species showed that mRNAs 2 and 3 were smaller than the corresponding transmissible gastroenteritis virus (TGEV) mRNA species (Page et al. (1991) J. Gen. Virol. 72, 579-587). Sequence analysis showed that mRNA 3 was smaller due to the presence of a new putative RNA-leader binding site upstream of the PRCV ORF-3 gene. However, this observation did not explain the deletion observed in PRCV mRNA 2. Polymerase chain reaction (PCR) was used to generate cDNA from the 3' coding region of the putative polymerase gene to the poly (A) tail of PRCV for comparison to the equivalent region from TGEV. The PRCV S protein was found to consist of 1225 amino acids, which had 98% similarity to the TGEV S protein. However, the PRCV S gene contained a 672 nucleotide deletion, corresponding to 224 amino acids (residues 21 to 245 in TGEV S protein), 59 nucleotides downstream of the S gene initiation codon. The PRCV genome from the ORF-3 gene to the poly (A) tail was sequenced for comparison to TGEV in order to identify other potential differences between the two viruses. Four ORFs were identified that showed 98% similarity to the TGEV ORF-4, M, N and ORF-7 genes. No other deletions or any PRCV specific sequences were identified.

摘要

先前对猪呼吸道冠状病毒(PRCV)mRNA种类的分析表明,mRNA 2和3比相应的传染性胃肠炎病毒(TGEV)mRNA种类小(Page等人,(1991年)《普通病毒学杂志》72卷,579 - 587页)。序列分析表明,mRNA 3较小是因为在PRCV ORF - 3基因上游存在一个新的假定RNA前导序列结合位点。然而,这一观察结果并不能解释在PRCV mRNA 2中观察到的缺失。聚合酶链反应(PCR)用于从假定的聚合酶基因的3'编码区到PRCV的聚(A)尾生成cDNA,以便与TGEV的等效区域进行比较。发现PRCV S蛋白由1225个氨基酸组成,与TGEV S蛋白有98%的相似性。然而,PRCV S基因包含一个672个核苷酸的缺失,对应于224个氨基酸(TGEV S蛋白中的第21至245位残基),位于S基因起始密码子下游59个核苷酸处。对从ORF - 3基因到聚(A)尾的PRCV基因组进行测序,以便与TGEV进行比较,以确定这两种病毒之间的其他潜在差异。鉴定出四个与TGEV ORF - 4、M、N和ORF - 7基因有98%相似性的开放阅读框。未发现其他缺失或任何PRCV特异性序列。

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