Pfeiffer B, Thomson B, Chandran B
Department of Microbiology, Molecular Genetics and Immunology, University of Kansas Medical Center, Kansas City 66160, USA.
J Virol. 1995 Jun;69(6):3490-500. doi: 10.1128/JVI.69.6.3490-3500.1995.
The glycoprotein complex gp82-gp105 is a major virion envelope glycoprotein complex of human herpesvirus 6 variant A (HHV-6A) and consists of a number of related polypeptides. Monoclonal antibodies (MAbs) 2D4, 2D6, and 13D6 against this glycoprotein complex neutralized HHV-6A infectivity. We have previously reported the isolation, mapping, and characterization of a portion of the viral genomic DNA fragment encoding the gp82-gp105 complex and the identification of the neutralizing epitope (B. Pfeiffer, Z. N. Berneman, F. Neipel, C. K. Chang, S. Tirwatnapong, and B. Chandran, J. Virol. 67:4611-4620, 1993). This gene was further characterized by the identification of a 2.3-kb genomic fragment and by the identification of a 2.5-kb cDNA clone. The genomic sequence contains a short open reading frame (ORF) encoding the epitope recognized by the MAbs. The identified cDNA showed specificity for HHV-6 in Southern blot analysis with viral DNA. In Northern (RNA) blot analysis with total RNA from HHV-6A(GS)-infected cells, the cDNA insert specifically hybridized with several RNA species. Restriction mapping analysis localized this cDNA to the HHV-6A(U1102) genomic BamHI G fragment, at the right end of the unique long segment of the genome and to the SalI L and SalI O fragments within the left and right terminal direct repeat regions, respectively. In vitro transcription and translation of the cDNA revealed a polypeptide of about 88.5 kDa which was glycosylated in the presence of microsomal membranes to a polypeptide of approximately 104.2 kDa. Both polypeptides were immunoprecipiated by MAb 2D6, verifying the identity of the cDNA as encoding the gp105 in the gp82-gp105 complex. Sequence analysis of the cDNA revealed a large ORF potentially encoding a 650-amino-acid protein with 11 potential N-linked glycosylation sites and 18 cysteine residues. A potential membrane-spanning domain is located only near the amino terminus of the putative protein, indicating that gp105 may be a class 2 glycoprotein. Comparison of the cDNA nucleotide sequence with sequences from HHV-6A(U1102) genomic BamHI G and SalI L fragments revealed that the gene encoding gp105 contains 12 exons, spanning over 20 kb of the viral genome, with intron 1 spanning about 8 kb of genomic DNA. The first exon of the cDNA mapped to the right and left terminal direct repeats, while the other exons mapped within the unique long segment of the genome.(ABSTRACT TRUNCATED AT 400 WORDS)
糖蛋白复合物gp82 - gp105是人类疱疹病毒6型A变体(HHV - 6A)主要的病毒体包膜糖蛋白复合物,由多种相关多肽组成。针对该糖蛋白复合物的单克隆抗体(MAb)2D4、2D6和13D6可中和HHV - 6A的感染性。我们之前报道了编码gp82 - gp105复合物的部分病毒基因组DNA片段的分离、定位和特征分析,以及中和表位的鉴定(B. Pfeiffer、Z. N. Berneman、F. Neipel、C. K. Chang、S. Tirwatnapong和B. Chandran,《病毒学杂志》67:4611 - 4620,1993年)。通过鉴定一个2.3 kb的基因组片段和一个2.5 kb的cDNA克隆,对该基因进行了进一步表征。基因组序列包含一个短开放阅读框(ORF),编码单克隆抗体识别的表位。在与病毒DNA的Southern印迹分析中,鉴定出的cDNA显示出对HHV - 6的特异性。在对HHV - 6A(GS)感染细胞的总RNA进行Northern(RNA)印迹分析时,cDNA插入片段与几种RNA物种特异性杂交。限制性图谱分析将该cDNA定位到HHV - 6A(U1102)基因组的BamHI G片段,位于基因组独特长片段的右端,以及分别位于左右末端直接重复区域内的SalI L和SalI O片段。cDNA的体外转录和翻译产生了一个约88.5 kDa的多肽,该多肽在微粒体膜存在的情况下糖基化成为一个约104.2 kDa的多肽。这两种多肽都被单克隆抗体2D6免疫沉淀,证实该cDNA编码gp82 - gp105复合物中的gp105。cDNA的序列分析揭示了一个大的ORF,可能编码一个具有11个潜在N连接糖基化位点和18个半胱氨酸残基的650个氨基酸的蛋白质。一个潜在的跨膜结构域仅位于推定蛋白质的氨基末端附近,表明gp105可能是一种2类糖蛋白。将cDNA核苷酸序列与HHV - 6A(U1102)基因组BamHI G和SalI L片段的序列进行比较,发现编码gp105的基因包含12个外显子,跨越病毒基因组超过20 kb,其中内含子1跨越约8 kb的基因组DNA。cDNA的第一个外显子定位到左右末端直接重复序列,而其他外显子定位在基因组的独特长片段内。(摘要截断于400字)