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首页> 外文期刊>Journal of Virology >The 160,000-Mr virion protein encoded at the right end of the herpesvirus saimiri genome is homologous to the 140,000-Mr membrane antigen encoded at the left end of the Epstein-Barr virus genome.
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The 160,000-Mr virion protein encoded at the right end of the herpesvirus saimiri genome is homologous to the 140,000-Mr membrane antigen encoded at the left end of the Epstein-Barr virus genome.

机译:在Herpesvirus Saimiri基因组右端编码的160,000-mr病毒蛋白蛋白与在Epstein-Barr病毒基因组左端编码的140,000-mr膜抗原同源。

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摘要

The sequence of 4.4 kilobase pairs (kbp) from the conventional right terminus of the A + T-rich light-DNA (L-DNA) sequences of the herpesvirus saimiri (HVS) genome contains a leftward-directed open reading frame (ORF) for a 1,299-residue protein. The molecular weight predicted for the protein (143,000) is in good agreement with the estimates of 150,000 to 160,000 for the major nonglycosylated polypeptide of the virion tegument (the 160K polypeptide), previously shown to be encoded by this region of the genome. The first initiation codon of the ORF is only 250 nucleotides from the junction of the L-DNA component with the G + C-rich terminal reiterations (i.e., heavy or H-DNA) of the genome. An unusually A + T-rich sequence (43 of 45 nucleotides are A or T, relative to a mean composition of 40% G + C for the ORF) occurs some 75 bp 5' to this initiation codon, and the first adenylation signal (AATAAA) on this DNA strand occurs 18 bp 3' to the termination codon. The amino acid sequence predicted for the 160K protein of HVS is homologous over most of its length to the 1,318-residue protein encoded by the leftmost major ORF of the G + C-rich genome of Epstein-Barr virus (BNRF1, the 140K nonglycosylated membrane antigen). No homology to either of these proteins is evident among the products predicted from the complete sequence of the alpha herpesvirus varicella-zoster virus. Thus gamma herpesviruses with coding sequences which differ in mean nucleotide composition by some 20% G + C have homologous proteins encoded at similar positions with respect to genome termini, with the right end of HVS being homologous to the left end of Epstein-Barr virus.
机译:来自Herpesvirus Saimiri(HVS)基因组的A + T富型光DNA(L-DNA)序列的常规右末端的4.4千碱基对(KBP)序列含有左侧定向的开放阅读框架(ORF)一个1,299-残基蛋白。对蛋白质(143,000)预测的分子量与50,000至160,000的估计值为150,000至160,000,以便在基因组的该区域编码,以前所示的前后核心化的多肽。 ORF的第一发起密码子仅是来自L-DNA组分的结合的250个核苷酸,其基因组的G + C的末端重新研(即重或H-DNA)。异常A + T-富含富含+ T-富含核苷酸的序列(43个核苷酸,相对于ORF的40%G + C的平均组成)发生了一些75bp 5'到该起始密码子,以及第一个腺苷酸化信号(在该DNA股线上的AataAA发生在终端密码子上的18bp 3'。预测的HV蛋白预测的氨基酸序列在其大部分长度上与由Epstein-Barr病毒的G + C的G + C的基因组的最左边的术语编码的1,318-残基蛋白质相同(BNRF1,140K核化膜。抗原)。在从αHerpesvirus variCella-Zoster病毒的完整序列预测的产品中,对这些蛋白质中的任何一个都没有同源性。因此,γ疱疹病毒与一些20%G + C的平均核苷酸组合物不同的编码序列具有在相对于基因组末端的类似位置编码的同源蛋白质,HVS的右端在Epstein-Barr病毒的左端同源。

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