Abstract
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)
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- Ablashi D. V., Balachandran N., Josephs S. F., Hung C. L., Krueger G. R., Kramarsky B., Salahuddin S. Z., Gallo R. C. Genomic polymorphism, growth properties, and immunologic variations in human herpesvirus-6 isolates. Virology. 1991 Oct;184(2):545–552. doi: 10.1016/0042-6822(91)90424-a. [DOI] [PubMed] [Google Scholar]
- Aubin J. T., Agut H., Collandre H., Yamanishi K., Chandran B., Montagnier L., Huraux J. M. Antigenic and genetic differentiation of the two putative types of human herpes virus 6. J Virol Methods. 1993 Feb;41(2):223–234. doi: 10.1016/0166-0934(93)90129-f. [DOI] [PubMed] [Google Scholar]
- Aubin J. T., Collandre H., Candotti D., Ingrand D., Rouzioux C., Burgard M., Richard S., Huraux J. M., Agut H. Several groups among human herpesvirus 6 strains can be distinguished by Southern blotting and polymerase chain reaction. J Clin Microbiol. 1991 Feb;29(2):367–372. doi: 10.1128/jcm.29.2.367-372.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Balachandran N., Amelse R. E., Zhou W. W., Chang C. K. Identification of proteins specific for human herpesvirus 6-infected human T cells. J Virol. 1989 Jun;63(6):2835–2840. doi: 10.1128/jvi.63.6.2835-2840.1989. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chandran B., Tirawatnapong S., Pfeiffer B., Ablashi D. V. Antigenic relationships among human herpesvirus-6 isolates. J Med Virol. 1992 Aug;37(4):247–254. doi: 10.1002/jmv.1890370403. [DOI] [PubMed] [Google Scholar]
- Chang C. K., Balachandran N. Identification, characterization, and sequence analysis of a cDNA encoding a phosphoprotein of human herpesvirus 6. J Virol. 1991 Jun;65(6):2884–2894. doi: 10.1128/jvi.65.6.2884-2894.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chomczynski P., Sacchi N. Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction. Anal Biochem. 1987 Apr;162(1):156–159. doi: 10.1006/abio.1987.9999. [DOI] [PubMed] [Google Scholar]
- Chou S., Marousek G. I. Analysis of interstrain variation in a putative immediate-early region of human herpesvirus 6 DNA and definition of variant-specific sequences. Virology. 1994 Jan;198(1):370–376. doi: 10.1006/viro.1994.1044. [DOI] [PubMed] [Google Scholar]
- Chou S., Marousek G. I. Homology of the envelope glycoprotein B of human herpesvirus-6 and cytomegalovirus. Virology. 1992 Nov;191(1):523–528. doi: 10.1016/0042-6822(92)90224-d. [DOI] [PubMed] [Google Scholar]
- Dewhurst S., Chandran B., McIntyre K., Schnabel K., Hall C. B. Phenotypic and genetic polymorphisms among human herpesvirus-6 isolates from North American infants. Virology. 1992 Sep;190(1):490–493. doi: 10.1016/0042-6822(92)91240-u. [DOI] [PubMed] [Google Scholar]
- Efstathiou S., Lawrence G. L., Brown C. M., Barrell B. G. Identification of homologues to the human cytomegalovirus US22 gene family in human herpesvirus 6. J Gen Virol. 1992 Jul;73(Pt 7):1661–1671. doi: 10.1099/0022-1317-73-7-1661. [DOI] [PubMed] [Google Scholar]
- Ellinger K., Neipel F., Foà-Tomasi L., Campadelli-Fiume G., Fleckenstein B. The glycoprotein B homologue of human herpesvirus 6. J Gen Virol. 1993 Mar;74(Pt 3):495–500. doi: 10.1099/0022-1317-74-3-495. [DOI] [PubMed] [Google Scholar]
- Gompels U. A., Carss A. L., Sun N., Arrand J. R. Infectivity determinants encoded in a conserved gene block of human herpesvirus-6. DNA Seq. 1992;3(1):25–39. doi: 10.3109/10425179209039693. [DOI] [PubMed] [Google Scholar]
- Gong M., Kieff E. Intracellular trafficking of two major Epstein-Barr virus glycoproteins, gp350/220 and gp110. J Virol. 1990 Apr;64(4):1507–1516. doi: 10.1128/jvi.64.4.1507-1516.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hirt B. Selective extraction of polyoma DNA from infected mouse cell cultures. J Mol Biol. 1967 Jun 14;26(2):365–369. doi: 10.1016/0022-2836(67)90307-5. [DOI] [PubMed] [Google Scholar]
- Human herpesvirus-6 strain groups: a nomenclature. Arch Virol. 1993;129(1-4):363–366. doi: 10.1007/BF01316913. [DOI] [PubMed] [Google Scholar]
- Inoue N., Dambaugh T. R., Pellett P. E. Molecular biology of human herpesviruses 6A and 6B. Infect Agents Dis. 1993 Dec;2(6):343–360. [PubMed] [Google Scholar]
- Jarrett R. F., Gallagher A., Gledhill S., Jones M. D., Teo I., Griffin B. E. Variation in restriction map of MHV-6 genome. Lancet. 1989 Feb 25;1(8635):448–449. doi: 10.1016/s0140-6736(89)90052-4. [DOI] [PubMed] [Google Scholar]
- Josephs S. F., Ablashi D. V., Salahuddin S. Z., Jagodzinski L. L., Wong-Staal F., Gallo R. C. Identification of the human herpesvirus 6 glycoprotein H and putative large tegument protein genes. J Virol. 1991 Oct;65(10):5597–5604. doi: 10.1128/jvi.65.10.5597-5604.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Josephs S. F., Ablashi D. V., Salahuddin S. Z., Kramarsky B., Franza B. R., Jr, Pellett P., Buchbinder A., Memon S., Wong-Staal F., Gallo R. C. Molecular studies of HHV-6. J Virol Methods. 1988 Sep;21(1-4):179–190. doi: 10.1016/0166-0934(88)90064-x. [DOI] [PubMed] [Google Scholar]
- Kozak M. An analysis of 5'-noncoding sequences from 699 vertebrate messenger RNAs. Nucleic Acids Res. 1987 Oct 26;15(20):8125–8148. doi: 10.1093/nar/15.20.8125. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lawrence G. L., Chee M., Craxton M. A., Gompels U. A., Honess R. W., Barrell B. G. Human herpesvirus 6 is closely related to human cytomegalovirus. J Virol. 1990 Jan;64(1):287–299. doi: 10.1128/jvi.64.1.287-299.1990. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lindquester G. J., Pellett P. E. Properties of the human herpesvirus 6 strain Z29 genome: G + C content, length, and presence of variable-length directly repeated terminal sequence elements. Virology. 1991 May;182(1):102–110. doi: 10.1016/0042-6822(91)90653-s. [DOI] [PubMed] [Google Scholar]
- Liu D. X., Gompels U. A., Nicholas J., Lelliott C. Identification and expression of the human herpesvirus 6 glycoprotein H and interaction with an accessory 40K glycoprotein. J Gen Virol. 1993 Sep;74(Pt 9):1847–1857. doi: 10.1099/0022-1317-74-9-1847. [DOI] [PubMed] [Google Scholar]
- Martin M. E., Thomson B. J., Honess R. W., Craxton M. A., Gompels U. A., Liu M. Y., Littler E., Arrand J. R., Teo I., Jones M. D. The genome of human herpesvirus 6: maps of unit-length and concatemeric genomes for nine restriction endonucleases. J Gen Virol. 1991 Jan;72(Pt 1):157–168. doi: 10.1099/0022-1317-72-1-157. [DOI] [PubMed] [Google Scholar]
- Mount S. M. A catalogue of splice junction sequences. Nucleic Acids Res. 1982 Jan 22;10(2):459–472. doi: 10.1093/nar/10.2.459. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Neipel F., Ellinger K., Fleckenstein B. The unique region of the human herpesvirus 6 genome is essentially collinear with the UL segment of human cytomegalovirus. J Gen Virol. 1991 Sep;72(Pt 9):2293–2297. doi: 10.1099/0022-1317-72-9-2293. [DOI] [PubMed] [Google Scholar]
- Pellett P. E., Black J. B., Yamamoto M. Human herpesvirus 6: the virus and the search for its role as a human pathogen. Adv Virus Res. 1992;41:1–52. doi: 10.1016/s0065-3527(08)60034-2. [DOI] [PubMed] [Google Scholar]
- Pfeiffer B., Berneman Z. N., Neipel F., Chang C. K., Tirwatnapong S., Chandran B. Identification and mapping of the gene encoding the glycoprotein complex gp82-gp105 of human herpesvirus 6 and mapping of the neutralizing epitope recognized by monoclonal antibodies. J Virol. 1993 Aug;67(8):4611–4620. doi: 10.1128/jvi.67.8.4611-4620.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Qian G., Wood C., Chandran B. Identification and characterization of glycoprotein gH of human herpesvirus-6. Virology. 1993 May;194(1):380–386. doi: 10.1006/viro.1993.1272. [DOI] [PubMed] [Google Scholar]
- Rawlinson W. D., Barrell B. G. Spliced transcripts of human cytomegalovirus. J Virol. 1993 Sep;67(9):5502–5513. doi: 10.1128/jvi.67.9.5502-5513.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Salahuddin S. Z., Ablashi D. V., Markham P. D., Josephs S. F., Sturzenegger S., Kaplan M., Halligan G., Biberfeld P., Wong-Staal F., Kramarsky B. Isolation of a new virus, HBLV, in patients with lymphoproliferative disorders. Science. 1986 Oct 31;234(4776):596–601. doi: 10.1126/science.2876520. [DOI] [PubMed] [Google Scholar]
- Senapathy P., Shapiro M. B., Harris N. L. Splice junctions, branch point sites, and exons: sequence statistics, identification, and applications to genome project. Methods Enzymol. 1990;183:252–278. doi: 10.1016/0076-6879(90)83018-5. [DOI] [PubMed] [Google Scholar]
- Southern E. M. Detection of specific sequences among DNA fragments separated by gel electrophoresis. J Mol Biol. 1975 Nov 5;98(3):503–517. doi: 10.1016/s0022-2836(75)80083-0. [DOI] [PubMed] [Google Scholar]
- Suga S., Yoshikawa T., Asano Y., Yazaki T., Hirata S. Human herpesvirus-6 infection (exanthem subitum) without rash. Pediatrics. 1989 Jun;83(6):1003–1006. [PubMed] [Google Scholar]
- Thompson J., Choudhury S., Kashanchi F., Doniger J., Berneman Z., Frenkel N., Rosenthal L. J. A transforming fragment within the direct repeat region of human herpesvirus type 6 that transactivates HIV-1. Oncogene. 1994 Apr;9(4):1167–1175. [PubMed] [Google Scholar]
- Thomson B. J., Dewhurst S., Gray D. Structure and heterogeneity of the a sequences of human herpesvirus 6 strain variants U1102 and Z29 and identification of human telomeric repeat sequences at the genomic termini. J Virol. 1994 May;68(5):3007–3014. doi: 10.1128/jvi.68.5.3007-3014.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thomson B. J., Honess R. W. The right end of the unique region of the genome of human herpesvirus 6 U1102 contains a candidate immediate early gene enhancer and a homologue of the human cytomegalovirus US22 gene family. J Gen Virol. 1992 Jul;73(Pt 7):1649–1660. doi: 10.1099/0022-1317-73-7-1649. [DOI] [PubMed] [Google Scholar]
- Yamanishi K., Okuno T., Shiraki K., Takahashi M., Kondo T., Asano Y., Kurata T. Identification of human herpesvirus-6 as a causal agent for exanthem subitum. Lancet. 1988 May 14;1(8594):1065–1067. doi: 10.1016/s0140-6736(88)91893-4. [DOI] [PubMed] [Google Scholar]