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骆驼痘病毒A 型包涵体蛋白编码基因的特性分析及其与其他正痘病毒的序列比较。

Characterization of the gene encoding the A-type inclusion protein of camelpox virus and sequence comparison with other orthopoxviruses.

作者信息

Meyer H, Rziha H J

机构信息

Institute of Microbiology, Federal Armed Forces Medical Academy, Munich, Germany.

出版信息

J Gen Virol. 1993 Aug;74 ( Pt 8):1679-84. doi: 10.1099/0022-1317-74-8-1679.

DOI:10.1099/0022-1317-74-8-1679
PMID:8345359
Abstract

A gene was identified in camelpox virus strain CP-1 that is similar to the 160K gene of cowpox virus strain Brighton (BR) that encodes the A-type inclusion body protein (ATIP). The CP-1 gene was mapped, sequenced, and the presence of the ATIP-specific mRNA was demonstrated. The open reading frame [2178 nucleotides (nt)] was found at a similar position in the CP genome as the one reported for the cowpox virus 160K ATI gene. DNA sequence comparison revealed a deletion of two adjacent adenine residues relative to cowpox virus BR, generating a reading frame shift accompanied by the formation of a translational stop codon. An identical deletion has been described for vaccinia virus strain Western Reserve. The DNA sequence of the corresponding region of monkeypox virus strain Copenhagen revealed a deletion leading to a putative stop codon 75 nt upstream of the same stop codons in the camelpox and vaccinia virus genes. These findings are consistent with the expression of truncated ATIPs, of 94K in vaccinia and camelpox viruses and of 92K in monkeypox virus. In addition, a deletion of 789 bp could be localized downstream of the ATI open reading frame in camelpox virus isolates of different origin. This causes the transcription of a shortened ATI-specific mRNA (3.7 kb) relative to vaccinia and cowpox viruses (both 4.5 kb). The similarity observed in ATIP-encoding and flanking sequences might suggest that vaccinia and camelpox viruses are descended from a common ancestor.

摘要

在骆驼痘病毒株CP - 1中鉴定出一个基因,该基因与牛痘病毒株布莱顿(BR)的160K基因相似,后者编码A型包涵体蛋白(ATIP)。对CP - 1基因进行了定位、测序,并证实了ATIP特异性mRNA的存在。在CP基因组中发现的开放阅读框[2178个核苷酸(nt)]与报道的牛痘病毒160K ATI基因处于相似位置。DNA序列比较显示,相对于牛痘病毒BR,有两个相邻腺嘌呤残基缺失,导致阅读框移位并形成翻译终止密码子。痘苗病毒株西储也有相同的缺失情况。猴痘病毒株哥本哈根相应区域的DNA序列显示有一个缺失,导致在骆驼痘病毒和痘苗病毒基因中相同终止密码子上游75 nt处出现一个推定的终止密码子。这些发现与痘苗病毒和骆驼痘病毒中截短的94K ATIP以及猴痘病毒中截短的92K ATIP的表达一致。此外,在不同来源的骆驼痘病毒分离株中,可在ATI开放阅读框下游定位到一个789 bp的缺失。这导致相对于痘苗病毒和牛痘病毒(均为4.5 kb)转录出缩短的ATI特异性mRNA(3.7 kb)。在ATIP编码序列和侧翼序列中观察到的相似性可能表明痘苗病毒和骆驼痘病毒有共同的祖先。

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