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猫冠状病毒FIPV 79-1146基因组3'末端的序列分析:与猪冠状病毒TGEV的基因组比较显示存在大量插入序列。

Sequence analysis of the 3'-end of the feline coronavirus FIPV 79-1146 genome: comparison with the genome of porcine coronavirus TGEV reveals large insertions.

作者信息

De Groot R J, Andeweg A C, Horzinek M C, Spaan W J

机构信息

Institute of Virology, Veterinary Faculty, State University of Utrecht, The Netherlands.

出版信息

Virology. 1988 Dec;167(2):370-6. doi: 10.1016/s0042-6822(88)90097-9.

Abstract

The genetic information, carried on mRNA 6 of feline infectious peritonitis virus (FIPV) strain 79-1146, was determined by sequence analysis of cDNA clones derived from the 3' end of the FIPV genome. Two ORFs were found, encoding polypeptides of 11K (ORF-1) and 22K (ORF-2). The FIPV sequence was compared to the 3' end sequence of transmissible gastroenteritis virus (TGEV). ORF-1 has a homologous counterpart (ORF-X3) in the TGEV genome; both ORFs are located at the same position relative to the nucleocapsid gene. However, as a result of an in-frame insertion or deletion, ORF-1 is 69 nucleotides larger than ORF-X3. A similar event has occurred immediately downstream of ORF1: a 624-nucleotide segment, containing the complete ORF-2, is absent in the TGEV sequence. Most sequence similarity (98.5%) was found in the 3' noncoding sequences. ORF-X3 and ORF-1 are preceded by the sequence AACTAAAC, which is assumed to be the transcription-initiation signal in FIPV and TGEV (P.A. Kapke and D.A. Brian (1986) Virology 151, 41-49). By S1 nuclease analysis, the 5' end of FIPV RNA 6 was mapped immediately upstream of this sequence. A 700-nucleotide TGEV-specific RNA was found by cross-hybridization with an FIPV 3' end probe, suggesting that TGEV ORF-X3 is also carried on a separate mRNA. The differences at the 3' ends of the FIPV and TGEV genomes may be the result of RNA recombination events.

摘要

通过对源自猫传染性腹膜炎病毒(FIPV)79 - 1146株基因组3'端的cDNA克隆进行序列分析,确定了其mRNA 6所携带的遗传信息。发现了两个开放阅读框(ORF),分别编码11K(ORF - 1)和22K(ORF - 2)的多肽。将FIPV序列与传染性胃肠炎病毒(TGEV)的3'端序列进行了比较。ORF - 1在TGEV基因组中有一个同源对应物(ORF - X3);两个开放阅读框相对于核衣壳基因位于相同位置。然而,由于框内插入或缺失,ORF - 1比ORF - X3长69个核苷酸。在ORF1的紧邻下游也发生了类似事件:TGEV序列中不存在包含完整ORF - 2的624个核苷酸的片段。在3'非编码序列中发现了最高的序列相似性(98.5%)。ORF - X3和ORF - 1之前的序列为AACTAAAC,假定其为FIPV和TGEV中的转录起始信号(P.A. Kapke和D.A. Brian(1986年),《病毒学》151卷,41 - 49页)。通过S1核酸酶分析,FIPV RNA 6的5'端定位在该序列紧邻上游。通过与FIPV 3'端探针交叉杂交发现了一个700个核苷酸的TGEV特异性RNA,表明TGEV的ORF - X3也存在于一个单独的mRNA上。FIPV和TGEV基因组3'端的差异可能是RNA重组事件的结果。

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