Kopácek J, Kl'ucár L, Koptidesová D, Turna J, Pastorek J, Zelník V
Institute of Virology, Slovak Academy of Sciences, Bratislava Slovak Republic.
Virus Genes. 2000;20(2):107-15. doi: 10.1023/a:1008158228591.
The gene encoding the major capsid protein (MCP) VP5 of herpesvirus of turkeys (HVT) was identified and sequenced. It has a single open reading frame of 4236 nucleotides encoding 1412 aa protein. The gene is flanked by VP23 and UL20 sequences and is localized in the unique long region (UL) within the BamHI-B fragment. Comparison of amino acid homology has shown its clear position among the alpha-herpesviruses rather than beta- or gamma-herpesviruses. The VP5 is expressed from polycistronic mRNA together with the UL20 and the VP23 genes. The 7,2 kb RNA transcript is lacking any promoter elements or polyA signal in intergenomic regions between VP5 and UL20 or VP5 and VP23 genes, respectively. Multiple alignment of known major capsid protein sequences of all herpesvirus groups revealed presence of seven highly homologous clusters suggesting-that the corresponding protein domains might play an important role in folding of MCP and assembly of herpesvirus capsid.
火鸡疱疹病毒(HVT)主要衣壳蛋白(MCP)VP5的编码基因被鉴定并测序。它有一个4236个核苷酸的单一开放阅读框,编码1412个氨基酸的蛋白质。该基因两侧是VP23和UL20序列,位于BamHI - B片段内的独特长区域(UL)。氨基酸同源性比较显示了它在α疱疹病毒中而非β或γ疱疹病毒中的明确位置。VP5与UL20和VP23基因一起从多顺反子mRNA表达。7.2 kb的RNA转录本在VP5与UL20或VP5与VP23基因之间的基因组间区域分别缺乏任何启动子元件或多聚腺苷酸信号。所有疱疹病毒组已知主要衣壳蛋白序列的多重比对显示存在七个高度同源的簇,表明相应的蛋白质结构域可能在MCP折叠和疱疹病毒衣壳组装中起重要作用。