Nucleotide sequences of glycoprotein I and E genes of equine herpesvirus type 4
The nucleotide sequences of the glycoprotein I (gI) and E (gE) genes of equine herpesvirus type 4 (EHV-4) strain TH20 were determined. The predicted region encoding the EHV-4 gI gene is 1,263 nucleotides, corresponding to a polypeptide of 420 amino acids in length. The predicted region encoding the...
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Published in | Journal of Veterinary Medical Science Vol. 60; no. 2; pp. 219 - 225 |
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Main Authors | , , , , , , |
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Language | English |
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JAPANESE SOCIETY OF VETERINARY SCIENCE
01.02.1998
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Abstract | The nucleotide sequences of the glycoprotein I (gI) and E (gE) genes of equine herpesvirus type 4 (EHV-4) strain TH20 were determined. The predicted region encoding the EHV-4 gI gene is 1,263 nucleotides, corresponding to a polypeptide of 420 amino acids in length. The predicted region encoding the EHV-4 gE gene is 1,647 nucleotides, corresponding to a polypeptide of 548 amino aids in length. The EHV-4 gI and gE genes show 74% and 86% identity at the amino acid level with those of equine herpesvirus type 1 (EHV-1), respectively. Furthermore, we have found an open reading frame homologous to the EHV-1 gene 75, which overlaps in part with the 3' end of EHV-4 gE gene. These sequence data will be useful for development of a modified live vaccine against equine herpesvirus type 1 and 4 infections |
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AbstractList | The nucleotide sequences of the glycoprotein I (gI) and E (gE) genes of equine herpesvirus type 4 (EHV-4) strain TH20 were determined. The predicted region encoding the EHV-4 gI gene is 1,263 nucleotides, corresponding to a polypeptide of 420 amino acids in length. The predicted region encoding the EHV-4 gE gene is 1,647 nucleotides, corresponding to a polypeptide of 548 amino aids in length. The EHV-4 gI and gE genes show 74% and 86% identity at the amino acid level with those of equine herpesvirus type 1 (EHV-1), respectively. Furthermore, we have found an open reading frame homologous to the EHV-1 gene 75, which overlaps in part with the 3' end of EHV-4 gE gene. These sequence data will be useful for development of a modified live vaccine against equine herpesvirus type 1 and 4 infections The nucleotide sequences of the glycoprotein I (gI) and E (gE) genes of equine herpesvirus type 4 (EHV-4) strain TH20 were determined. The predicted region encoding the EHV-4 gI gene is 1,263 nucleotides, corresponding to a polypeptide of 420 amino acids in length. The predicted region encoding the EHV-4 gE gene is 1,647 nucleotides, corresponding to a polypeptide of 548 amino acids in length. The EHV-4 gI and gE genes show 74% and 85% identity at the amino acid level with those of equine herpesvirus type 1 (EHV-1), respectively. Furthermore, we have found an open reading frame homologous to the EHV-1 gene 75, which overlaps in part with the 3' end of EHV-4 gE gene. These sequence data will be useful for development of a modified live vaccine against equine herpesvirus type 1 and 4 infections. The nucleotide sequences of the glycoprotein I (gI) and E (gE) genes of equine herpesvirus type 4 (EHV-4) strain TH20 were determined. The predicted region encoding the EHV-4 gI gene is 1,263 nucleotides, corresponding to a polypeptide of 420 amino acids in length. The predicted region encoding the EHV-4 gE gene is 1,647 nucleotides, corresponding to a polypeptide of 548 amino acids in length. The EHV-4 gI and gE genes show 74% and 85% identity at the amino acid level with those of equine herpesvirus type 1 (EHV-1), respectively. Furthermore, we have found an open reading frame homologous to the EHV-1 gene 75, which overlaps in part with the 3' end of EHV-4 gE gene. These sequence data will be useful for development of a modified live vaccine against equine herpesvirus type 1 and 4 infections.The nucleotide sequences of the glycoprotein I (gI) and E (gE) genes of equine herpesvirus type 4 (EHV-4) strain TH20 were determined. The predicted region encoding the EHV-4 gI gene is 1,263 nucleotides, corresponding to a polypeptide of 420 amino acids in length. The predicted region encoding the EHV-4 gE gene is 1,647 nucleotides, corresponding to a polypeptide of 548 amino acids in length. The EHV-4 gI and gE genes show 74% and 85% identity at the amino acid level with those of equine herpesvirus type 1 (EHV-1), respectively. Furthermore, we have found an open reading frame homologous to the EHV-1 gene 75, which overlaps in part with the 3' end of EHV-4 gE gene. These sequence data will be useful for development of a modified live vaccine against equine herpesvirus type 1 and 4 infections. |
Author | Miyazawa, T Mikami, T Matsumura, T Damiani, A.M. (Tokyo Univ. (Japan). Faculty of Agriculture) Maeda, K Kai, C Yokoyama, N |
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Cites_doi | 10.1007/BF01309883 10.1016/0042-6822(89)90604-1 10.1128/JVI.61.2.600-603.1987 10.1016/0022-2836(90)90223-9 10.1006/viro.1995.9959 10.1093/nar/14.11.4683 10.1128/JVI.61.9.2764-2769.1987 10.1292/jvms.54.207 10.1099/0022-1317-69-7-1575 10.1128/JVI.60.1.185-193.1986 10.1128/JVI.65.5.2320-2326.1991 10.1016/S0065-3527(08)60060-3 10.1016/0378-1119(88)90330-7 10.1093/nar/13.3.953 10.1099/0022-1317-74-9-1959 10.1016/0042-6822(90)90305-B 10.1099/0022-1317-75-6-1245 10.1099/0022-1317-71-8-1793 10.1016/0092-8674(86)90762-2 10.1099/0022-1317-67-9-1759 10.1016/0022-2836(82)90515-0 10.1099/0022-1317-71-12-2969 10.1006/viro.1994.1139 10.1099/0022-1317-74-10-2201 10.1128/JVI.63.3.1123-1133.1989 10.1016/S0092-8674(85)80007-6 10.1128/JVI.66.5.3032-3041.1992 10.1128/JVI.69.11.7087-7098.1995 10.1099/0022-1317-75-9-2311 10.1016/S0042-6822(95)80048-4 10.1016/0042-6822(81)90092-1 10.1016/0022-2836(85)90320-1 10.1016/0042-6822(92)90706-U 10.1006/viro.1995.1202 10.1016/0264-410X(95)00080-K 10.1016/0042-6822(92)91200-E 10.1128/JVI.67.7.3961-3968.1993 |
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References | 7. Crabb, B. S., Nagesha, H. S. and Studdert, M. J. 1992. Identification of equine herpesvirus 4 glycoprotein G: a type-specific, secreted glycoprotein. Virology 190: 143-154. 15. Higgins, D. G. and Sharp, P. M. 1988. CLUSTAL: a package for performing multiple sequence alignment on a microcomputer. Gene 73: 237-244. 23. Matsumura, T., Sugiura, T., Imagawa, H., Fukunaga, Y. and Kamada, M. 1992. Epizootiological aspects of the type 1 and type 4 equine herpesvirus infections among horse populations. J. Vet. Med. Sci. 54: 207-211. 21. Kyte, J. and Doolittle, R. F. 1982. A simple method for displaying the hydropathic character of a protein. J. Mol. Biol. 157: 105-132. 22. Leung-Tack, P., Audonnet, J. C. and Riviere, M. 1994. The complete DNA sequence and the genetic organization of the short unique region (Us) of the bovine herpesvirus 1 (ST strain). Virology 199: 409-421. 1. Audonnet, J. C., Winslow, J., Allen, G. and Paoletti, E. 1990. Equine herpesvirus type 1 unique short fragment encodes glycoproteins with homology to herpes simplex virus type 1 gD, gI, gE. J. Gen. Virol. 71: 2969-2978. 19. Kost, T. A., Jones, E. V., Smith, K. M., Reed, A. P., Brown, A. L. and Miller, T. J. 1989. Biological evaluation of glycoproteins mapping to two distinct mRNAs within the BamHI fragment 7 of pseudorabies virus: expression of the coding regions by vaccinia virus. Virology 171: 365-376. 25. Mettenleiter, T. C., Schreurs, C., Zuckermann, F. and Ben-Porat, T. 1987. Role of pseudorabies virus glycoprotein gI in virus release from infected cells. J. Virol. 61: 2764-2769. 31. Ostlund, E. N. 1993. The equine herpesvirus. Vet. Clin. North Am. 9: 283-294. 34. Rixon, F. J. and McGeoch, D. J. 1985. Detailed analysis of the mRNAs mapping in the short unique region of herpes simplex virus type 1. Nucleic Acids Res. 13: 953-973. 40. Whittaker, G. R., Riggio, M. P., Halliburton, I. W., Killington, R. A., Allen, G. P. and Meredith, D. M. 1991. Antigenic and protein sequence homology between VP 13/14, a herpes simplex virus type 1 tegument protein, and gp10, a glycoprotein of equine herpesvirus 1 and 4. J. Virol. 65: 2320-2326. 18. Kawakami, Y., Kaji, T., Ishizaki, R., Shimizu, T. and Matumoto, M. 1962. Etiologic study on an outbreak of acute respiratory disease among colts due to equine rhinopneumonitis virus. Jpn. J. Exp. Med. 32: 211-229. 24. McGeoch, D. J., Dolan, A., Donald, S. and Rixon, F. J. 1985. Sequence determination and genetic content of the short unique region in the genome of herpes simplex virus type 1. J. Mol. Biol. 181: 1-13. 38. van Engelenburg, F. A. C., Kaashoek, M. J., Rijsewijk, F. A. M., van den Burg, L., Moerman, A., Gielkens, A. L. J. and van Oirschot, J. T. 1994. A glycoprotein E deletion mutant of bovine herpesvirus 1 is avirulent in calves. J. Gen. Virol. 75: 2311-2318. 10. Cullinane, A. A., Rixon, F. J. and Davison, A. J. 1988. Characterization of the genome of equine herpesvirus 1 subtype 2. J. Gen. Virol. 69: 1575-1590. 39. von Heijne, G. 1986. A new method for predicting signal sequence cleavage sites. Nucleic Acids Res. 14: 4683-4690. 12. Dingwell, K. S., Doering, L. C. and Johnson, D. C. 1995. Glycoproteins E and I facilitate neuron-to-neuron spread of herpes simplex type 1 virus. J. Virol. 69: 7087-7098. 13. Georgopoulou, U., Michaelidou, A., Roizman, B. and Mavromara-Nazos, P. 1993. Identification of a new transcriptional unit that yields a gene product within the unique sequences of the short component of the herpes simplex virus 1 genome. J. Virol. 67: 3961-3968. 14. Henry, B. E., Robinson, R. A., Dauenhauer, S. A., Atherton, S. S., Hayward, G. S. and O'Callaghan, D. J. 1981. Structure of the genome of equine herpesvirus type 1. Virology 115: 97-114. 37. Telford, E. R., Watson, M. S., McBride, K. and Davison, A. J. 1992. The DNA sequence of equine herpesvirus-1. Virology 189: 304-316. 30. Nicolson, L. and Onions, D. E. 1990. The nucleotide sequence of the equine herpesvirus 4 gC gene homologue. Virology 179: 378-387. 5. Bucher, P. 1990. Weight matrix descriptions of four eukaryotic RNA polymerase II promoter elements derived from 502 unrelated promoter sequences. J. Mol. Biol. 212: 563-578. 35. Roizman, B., Desrosiers, R. C., Fleckenstein, B., Lopez, C., Minson, A. C. and Studdert, M. J. 1995. Herpesviridae. pp. 114-127. In: Classification and Nomenclature of Viruses (Murphy, F. A., Fauquet, C. M., Bishop, D. H. L., Ghabrial, S. A., Jarvis, A. W., Martelli, G. P., Mayo, M. A. and Summers, M. D. eds.), Springer, Wien New York (Arch Virol. [Suppl.] 10). 9. Cullinane, A. A., Neilan, J., Wilson, L., Davison, A. J. and Allen, G. 1993. The DNA sequence of the equine herpesvirus 4 gene encoding glycoprotein gp17/18, the homologue of herpes simplex virus glycoprotein gD. J. Gen. Virol. 74: 1959-1964. 11. Davison, A. J. and Scott, J. E. 1986. The complete DNA sequence of varicella-zoster virus. J. Gen. Virol. 67: 1759-1816. 2. Balan, P., Davis-Poynter, N., Bell, S., Atkinson, H., Browne, H. and Minson, T. 1994. An analysis of the in vitro and in vivo phenotypes of mutant herpes simplex virus type 1 lacking glycoproteins gG, gE, gI or the putative gJ. J. Gen. Virol. 75: 1245-1258. 27. Nagesha, H. S., McNeil, J. R., Ficorilli, N. and Studdert, M. J. 1992. Cloning and restriction endonuclease mapping of the genome of an equine herpesvirus 4 (equine rhinopneumonitis virus), strain 405/76. Arch. Virol. 124: 379-387. 32. Petrovskis, E. A., Timmins, J. G. and Post, L. E. 1986. Use of lgt11 to isolate genes for two pseudorabies virus glycoproteins with homology to herpes simplex virus and varicella-zoster virus glycoproteins. J. Virol. 60: 185-193. 29. Nicolson, L., Cullinane, A. A. and Onions, D. E. 1990. The nucleotide sequence of an equine herpesvirus 4 gene homologue of the herpes simplex virus 1 glycoprotein H gene. J. Gen. Virol. 71: 1793-1800. 6. Card, J. P., Whealy, M. E., Robbins, A. K. and Enquist, L. W. 1992. Pseudorabies virus envelope glycoprotein gI influences both neurotropism and virulence during infection of the rat visual system. J. Virol. 66: 3032-3041. 26. Nagesha, H. S., Crabb, B. S. and Studdert, M. J. 1993. Analysis of the nucleotide sequence of five genes at the left end of the unique short region of the equine herpesvirus 4 genome. Arch. Virol. 128: 143-154. 36. Sussman, M. D., Maes, R. K., Kruger, J. M., Spatz, S. J. and Venta, J. 1995. A feline herpesvirus-1 recombinant with a deletion in the genes for glycoproteins gI and gE is effective as a vaccine for feline rhinotracheitis. Virology 214: 12-20. 33. Riggio, M. P., Cullinane, A. A. and Onions, D. E. 1989. Identification and nucleotide sequence of the glycoprotein gB gene of equine herpesvirus 4. J. Virol. 63: 1123-1133. 41. Willemse, M. J., Chalmers, W. S. K. and Sondermeijer, P. J. A. 1996. In vivo properties of a feline herpesvirus type 1 mutant carrying a lac Z insertion at the gI locus of the unique short segment. Vaccine 14: 1-5. 42. Willemse, M. J., Strijdveen, I. G. L., van Schooneveld, S. H. B., van den Berg, M. C. and Sondermeijer, J. A. 1995. Transcriptional analysis of the short segment of the feline herpesvirus type 1 genome and insertional mutagenesis of the unique reading frame. Virology 208: 704-711. 16. Hirai, K., Nakajima, K., Ikuta, K., Kirisawa, R., Kawakami, Y., Mikami, T. and Kato, S. 1986. Similarities and dissimilarities in the structure and expression of viral genomes of various virus strains immunologically related to Marek's disease virus. Arch. Virol. 89: 113-130. 8. Crabb, B. S. and Studdert, M. J. 1995. Equine herpesvirus 4 (equine rhinopneumonitis virus) and 1 (equine abortion virus). Adv. Virus Res. 45: 153-190. 17. Jacobs, L., Mulder, W. A. M., van Oirschot, J. T., Gielkens, A. L. J. and Kimman, T. G. 1993. Deleting two amino acids in glycoprotein gI of pseudorabies virus decreases virulence and neurotropism for pigs, but does not affect immunogenicity. J. Gen. Virol. 74: 2201-2206. 4. Brunovskis, P. and Velicer, L. F. 1995. The Marek's disease virus (MDV) unique short region: alphaherpesvirus-homologous, fowlpox virus-homologous, and MDV-specific genes. Virology 206: 324-338. 28. Neidhardt, H., Schröder, C. H. and Kaerner, H. C. 1987. Herpes simplex virus type 1 glycoprotein E is not indispensable for viral infectivity. J. Virol. 61: 600-603. 3. Birnsteil, M. L., Busslinger, M. and Strub, K. 1985. Transcription termination and 3' processing: the end is in site! Cell 41: 349-359. 20. Kozak, M. 1986. Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes. Cell 44: 283-292. 22 Neidhardt, H., Schröder, C (28) 1987; 61 MATSUMURA T (23) 1992; 54 Ostlund, E. N. (31) 1993; 9 Hirai, K., Nakajima, K., Ikuta, K. (16) 1986; 89 (38) 1994; 75 Birnsteil, M. L., Busslinger, M. an (3) 1985; 41 (9) 1993; 74 (1) 1990; 71 (13) 1993; 67 von Heijne, G. (39) 1986; 14 (4) 1995; 206 (40) 1991; 65 (2) 1994; 75 Kyte, J. and Doolittle, R.F. (21) 1982; 157 Kost, T. A., Jones, E. V., Smith, K (19) 1989; 171 McGeoch, D. J., Dolan, A., Donald (24) 1985; 181 Davison, A. J. and Scott, J. E. (11) 1986; 67 Crabb, B. S. and Studdert, M. J. (8) 1995; 45 30 Mettenleiter, T. C., Schreurs, C. (25) 1987; 61 36 15 37 (6) 1992; 66 Kawakami, Y., Kaji, T., Ishizaki, R (18) 1962; 32 Cullinane, A. A., Rixon, F. J. and (10) 1988; 69 (29) 1990; 71 (5) 1990; 212 (12) 1995; 69 (17) 1993; 74 (27) 1992; 124 (26) 1993; 128 Roizman, B., Desrosiers, R. C., Fle (35) 1995 7 Kozak, M. (20) 1986; 44 Riggio, M. P., Cullinane, A. A. and (33) 1989; 63 Petrovskis, E. A., Timmins, J. G. a (32) 1986; 60 Henry, B. E., Robinson, R. A., Daue (14) 1981; 115 41 42 Rixon, F. J. and McGeoch, D. J. (34) 1985; 13 |
References_xml | – reference: 27. Nagesha, H. S., McNeil, J. R., Ficorilli, N. and Studdert, M. J. 1992. Cloning and restriction endonuclease mapping of the genome of an equine herpesvirus 4 (equine rhinopneumonitis virus), strain 405/76. Arch. Virol. 124: 379-387. – reference: 29. Nicolson, L., Cullinane, A. A. and Onions, D. E. 1990. The nucleotide sequence of an equine herpesvirus 4 gene homologue of the herpes simplex virus 1 glycoprotein H gene. J. Gen. Virol. 71: 1793-1800. – reference: 42. Willemse, M. J., Strijdveen, I. G. L., van Schooneveld, S. H. B., van den Berg, M. C. and Sondermeijer, J. A. 1995. Transcriptional analysis of the short segment of the feline herpesvirus type 1 genome and insertional mutagenesis of the unique reading frame. Virology 208: 704-711. – reference: 36. Sussman, M. D., Maes, R. K., Kruger, J. M., Spatz, S. J. and Venta, J. 1995. A feline herpesvirus-1 recombinant with a deletion in the genes for glycoproteins gI and gE is effective as a vaccine for feline rhinotracheitis. Virology 214: 12-20. – reference: 1. Audonnet, J. C., Winslow, J., Allen, G. and Paoletti, E. 1990. Equine herpesvirus type 1 unique short fragment encodes glycoproteins with homology to herpes simplex virus type 1 gD, gI, gE. J. Gen. Virol. 71: 2969-2978. – reference: 9. Cullinane, A. A., Neilan, J., Wilson, L., Davison, A. J. and Allen, G. 1993. The DNA sequence of the equine herpesvirus 4 gene encoding glycoprotein gp17/18, the homologue of herpes simplex virus glycoprotein gD. J. Gen. Virol. 74: 1959-1964. – reference: 4. Brunovskis, P. and Velicer, L. F. 1995. The Marek's disease virus (MDV) unique short region: alphaherpesvirus-homologous, fowlpox virus-homologous, and MDV-specific genes. Virology 206: 324-338. – reference: 33. Riggio, M. P., Cullinane, A. A. and Onions, D. E. 1989. Identification and nucleotide sequence of the glycoprotein gB gene of equine herpesvirus 4. J. Virol. 63: 1123-1133. – reference: 8. Crabb, B. S. and Studdert, M. J. 1995. Equine herpesvirus 4 (equine rhinopneumonitis virus) and 1 (equine abortion virus). Adv. Virus Res. 45: 153-190. – reference: 14. Henry, B. E., Robinson, R. A., Dauenhauer, S. A., Atherton, S. S., Hayward, G. S. and O'Callaghan, D. J. 1981. Structure of the genome of equine herpesvirus type 1. Virology 115: 97-114. – reference: 3. Birnsteil, M. L., Busslinger, M. and Strub, K. 1985. Transcription termination and 3' processing: the end is in site! Cell 41: 349-359. – reference: 16. Hirai, K., Nakajima, K., Ikuta, K., Kirisawa, R., Kawakami, Y., Mikami, T. and Kato, S. 1986. Similarities and dissimilarities in the structure and expression of viral genomes of various virus strains immunologically related to Marek's disease virus. Arch. Virol. 89: 113-130. – reference: 13. Georgopoulou, U., Michaelidou, A., Roizman, B. and Mavromara-Nazos, P. 1993. Identification of a new transcriptional unit that yields a gene product within the unique sequences of the short component of the herpes simplex virus 1 genome. J. Virol. 67: 3961-3968. – reference: 28. Neidhardt, H., Schröder, C. H. and Kaerner, H. C. 1987. Herpes simplex virus type 1 glycoprotein E is not indispensable for viral infectivity. J. Virol. 61: 600-603. – reference: 41. Willemse, M. J., Chalmers, W. S. K. and Sondermeijer, P. J. A. 1996. In vivo properties of a feline herpesvirus type 1 mutant carrying a lac Z insertion at the gI locus of the unique short segment. Vaccine 14: 1-5. – reference: 2. Balan, P., Davis-Poynter, N., Bell, S., Atkinson, H., Browne, H. and Minson, T. 1994. An analysis of the in vitro and in vivo phenotypes of mutant herpes simplex virus type 1 lacking glycoproteins gG, gE, gI or the putative gJ. J. Gen. Virol. 75: 1245-1258. – reference: 17. Jacobs, L., Mulder, W. A. M., van Oirschot, J. T., Gielkens, A. L. J. and Kimman, T. G. 1993. Deleting two amino acids in glycoprotein gI of pseudorabies virus decreases virulence and neurotropism for pigs, but does not affect immunogenicity. J. Gen. Virol. 74: 2201-2206. – reference: 38. van Engelenburg, F. A. C., Kaashoek, M. J., Rijsewijk, F. A. M., van den Burg, L., Moerman, A., Gielkens, A. L. J. and van Oirschot, J. T. 1994. A glycoprotein E deletion mutant of bovine herpesvirus 1 is avirulent in calves. J. Gen. Virol. 75: 2311-2318. – reference: 37. Telford, E. R., Watson, M. S., McBride, K. and Davison, A. J. 1992. The DNA sequence of equine herpesvirus-1. Virology 189: 304-316. – reference: 32. Petrovskis, E. A., Timmins, J. G. and Post, L. E. 1986. Use of lgt11 to isolate genes for two pseudorabies virus glycoproteins with homology to herpes simplex virus and varicella-zoster virus glycoproteins. J. Virol. 60: 185-193. – reference: 12. Dingwell, K. S., Doering, L. C. and Johnson, D. C. 1995. Glycoproteins E and I facilitate neuron-to-neuron spread of herpes simplex type 1 virus. J. Virol. 69: 7087-7098. – reference: 6. Card, J. P., Whealy, M. E., Robbins, A. K. and Enquist, L. W. 1992. Pseudorabies virus envelope glycoprotein gI influences both neurotropism and virulence during infection of the rat visual system. J. Virol. 66: 3032-3041. – reference: 31. Ostlund, E. N. 1993. The equine herpesvirus. Vet. Clin. North Am. 9: 283-294. – reference: 23. Matsumura, T., Sugiura, T., Imagawa, H., Fukunaga, Y. and Kamada, M. 1992. Epizootiological aspects of the type 1 and type 4 equine herpesvirus infections among horse populations. J. Vet. Med. Sci. 54: 207-211. – reference: 5. Bucher, P. 1990. Weight matrix descriptions of four eukaryotic RNA polymerase II promoter elements derived from 502 unrelated promoter sequences. J. Mol. Biol. 212: 563-578. – reference: 35. Roizman, B., Desrosiers, R. C., Fleckenstein, B., Lopez, C., Minson, A. C. and Studdert, M. J. 1995. Herpesviridae. pp. 114-127. In: Classification and Nomenclature of Viruses (Murphy, F. A., Fauquet, C. M., Bishop, D. H. L., Ghabrial, S. A., Jarvis, A. W., Martelli, G. P., Mayo, M. A. and Summers, M. D. eds.), Springer, Wien New York (Arch Virol. [Suppl.] 10). – reference: 34. Rixon, F. J. and McGeoch, D. J. 1985. Detailed analysis of the mRNAs mapping in the short unique region of herpes simplex virus type 1. Nucleic Acids Res. 13: 953-973. – reference: 40. Whittaker, G. R., Riggio, M. P., Halliburton, I. W., Killington, R. A., Allen, G. P. and Meredith, D. M. 1991. Antigenic and protein sequence homology between VP 13/14, a herpes simplex virus type 1 tegument protein, and gp10, a glycoprotein of equine herpesvirus 1 and 4. J. Virol. 65: 2320-2326. – reference: 7. Crabb, B. S., Nagesha, H. S. and Studdert, M. J. 1992. Identification of equine herpesvirus 4 glycoprotein G: a type-specific, secreted glycoprotein. Virology 190: 143-154. – reference: 11. Davison, A. J. and Scott, J. E. 1986. The complete DNA sequence of varicella-zoster virus. J. Gen. Virol. 67: 1759-1816. – reference: 10. Cullinane, A. A., Rixon, F. J. and Davison, A. J. 1988. Characterization of the genome of equine herpesvirus 1 subtype 2. J. Gen. Virol. 69: 1575-1590. – reference: 25. Mettenleiter, T. C., Schreurs, C., Zuckermann, F. and Ben-Porat, T. 1987. Role of pseudorabies virus glycoprotein gI in virus release from infected cells. J. Virol. 61: 2764-2769. – reference: 39. von Heijne, G. 1986. A new method for predicting signal sequence cleavage sites. Nucleic Acids Res. 14: 4683-4690. – reference: 24. McGeoch, D. J., Dolan, A., Donald, S. and Rixon, F. J. 1985. Sequence determination and genetic content of the short unique region in the genome of herpes simplex virus type 1. J. Mol. Biol. 181: 1-13. – reference: 26. Nagesha, H. S., Crabb, B. S. and Studdert, M. J. 1993. Analysis of the nucleotide sequence of five genes at the left end of the unique short region of the equine herpesvirus 4 genome. Arch. Virol. 128: 143-154. – reference: 18. Kawakami, Y., Kaji, T., Ishizaki, R., Shimizu, T. and Matumoto, M. 1962. Etiologic study on an outbreak of acute respiratory disease among colts due to equine rhinopneumonitis virus. Jpn. J. Exp. Med. 32: 211-229. – reference: 22. Leung-Tack, P., Audonnet, J. C. and Riviere, M. 1994. The complete DNA sequence and the genetic organization of the short unique region (Us) of the bovine herpesvirus 1 (ST strain). Virology 199: 409-421. – reference: 20. Kozak, M. 1986. Point mutations define a sequence flanking the AUG initiator codon that modulates translation by eukaryotic ribosomes. Cell 44: 283-292. – reference: 30. Nicolson, L. and Onions, D. E. 1990. The nucleotide sequence of the equine herpesvirus 4 gC gene homologue. Virology 179: 378-387. – reference: 15. Higgins, D. G. and Sharp, P. M. 1988. CLUSTAL: a package for performing multiple sequence alignment on a microcomputer. Gene 73: 237-244. – reference: 21. Kyte, J. and Doolittle, R. F. 1982. A simple method for displaying the hydropathic character of a protein. J. Mol. Biol. 157: 105-132. – reference: 19. Kost, T. A., Jones, E. V., Smith, K. M., Reed, A. P., Brown, A. L. and Miller, T. J. 1989. Biological evaluation of glycoproteins mapping to two distinct mRNAs within the BamHI fragment 7 of pseudorabies virus: expression of the coding regions by vaccinia virus. Virology 171: 365-376. – volume: 89 start-page: 113 issn: 0304-8608 year: 1986 ident: 16 publication-title: Arch. Virol. doi: 10.1007/BF01309883 – volume: 171 start-page: 365 issn: 0042-6822 issue: 2 year: 1989 ident: 19 publication-title: Virology doi: 10.1016/0042-6822(89)90604-1 – volume: 128 start-page: 143 issn: 0304-8608 issue: 1/2 year: 1993 ident: 26 publication-title: Arch. Virol. – volume: 61 start-page: 600 issn: 0022-538X issue: 2 year: 1987 ident: 28 publication-title: J. Virol. doi: 10.1128/JVI.61.2.600-603.1987 – volume: 212 start-page: 563 issn: 0022-2836 issue: 4 year: 1990 ident: 5 publication-title: J. Mol. Biol. doi: 10.1016/0022-2836(90)90223-9 – volume: 124 start-page: 379 issn: 0304-8608 issue: 3/4 year: 1992 ident: 27 publication-title: Arch. Virol. – ident: 36 doi: 10.1006/viro.1995.9959 – volume: 14 start-page: 4683 issn: 0305-1048 year: 1986 ident: 39 publication-title: Nucleic Acids Res. doi: 10.1093/nar/14.11.4683 – volume: 61 start-page: 2764 issn: 0022-538X issue: 9 year: 1987 ident: 25 publication-title: J. Virol. doi: 10.1128/JVI.61.9.2764-2769.1987 – volume: 54 start-page: 207 issn: 0916-7250 issue: 2 year: 1992 ident: 23 publication-title: J. Vet. Med. Sci. doi: 10.1292/jvms.54.207 – volume: 69 start-page: 1575 issn: 0022-1317 issue: 7 year: 1988 ident: 10 publication-title: J. Gen. Virol. doi: 10.1099/0022-1317-69-7-1575 – volume: 60 start-page: 185 issn: 0022-538X issue: 1 year: 1986 ident: 32 publication-title: J. Virol. doi: 10.1128/JVI.60.1.185-193.1986 – volume: 65 start-page: 2320 issn: 0022-538X issue: 5 year: 1991 ident: 40 publication-title: J. Virol. doi: 10.1128/JVI.65.5.2320-2326.1991 – volume: 45 start-page: 153 issn: 0065-3527 year: 1995 ident: 8 publication-title: Adv. Virus Res. doi: 10.1016/S0065-3527(08)60060-3 – ident: 15 doi: 10.1016/0378-1119(88)90330-7 – volume: 13 start-page: 953 issn: 0305-1048 issue: 3 year: 1985 ident: 34 publication-title: Nucleic Acids Res. doi: 10.1093/nar/13.3.953 – volume: 74 start-page: 1959 issn: 0022-1317 issue: 9 year: 1993 ident: 9 publication-title: J. Gen. Virol. doi: 10.1099/0022-1317-74-9-1959 – ident: 30 doi: 10.1016/0042-6822(90)90305-B – volume: 75 start-page: 1245 issn: 0022-1317 issue: 6 year: 1994 ident: 2 publication-title: J. Gen. Virol. doi: 10.1099/0022-1317-75-6-1245 – volume: 71 start-page: 1793 issn: 0022-1317 issue: 8 year: 1990 ident: 29 publication-title: J. Gen. Virol. doi: 10.1099/0022-1317-71-8-1793 – volume: 44 start-page: 283 issn: 0092-8674 issue: 2 year: 1986 ident: 20 publication-title: Cell doi: 10.1016/0092-8674(86)90762-2 – volume: 67 start-page: 1759 issn: 0022-1317 issue: 9 year: 1986 ident: 11 publication-title: J. Gen. Virol. doi: 10.1099/0022-1317-67-9-1759 – volume: 157 start-page: 105 issn: 0022-2836 issue: 1 year: 1982 ident: 21 publication-title: J. Mol. Biol. doi: 10.1016/0022-2836(82)90515-0 – volume: 71 start-page: 2969 issn: 0022-1317 issue: 12 year: 1990 ident: 1 publication-title: J. Gen. Virol. doi: 10.1099/0022-1317-71-12-2969 – ident: 22 doi: 10.1006/viro.1994.1139 – start-page: 114 year: 1995 ident: 35 – volume: 74 start-page: 2201 issn: 0022-1317 issue: 10 year: 1993 ident: 17 publication-title: J. Gen. Virol. doi: 10.1099/0022-1317-74-10-2201 – volume: 63 start-page: 1123 issn: 0022-538X issue: 3 year: 1989 ident: 33 publication-title: </bibserti> 1989. Identification and nucleotide sequence of the glycoprotein gB gene of equine herpesvirus 4. doi: 10.1128/JVI.63.3.1123-1133.1989 – volume: 41 start-page: 349 issn: 0092-8674 issue: 2 year: 1985 ident: 3 publication-title: Cell doi: 10.1016/S0092-8674(85)80007-6 – volume: 66 start-page: 3032 issn: 0022-538X issue: 5 year: 1992 ident: 6 publication-title: J. Virol. doi: 10.1128/JVI.66.5.3032-3041.1992 – volume: 69 start-page: 7087 issn: 0022-538X issue: 11 year: 1995 ident: 12 publication-title: J. Virol. doi: 10.1128/JVI.69.11.7087-7098.1995 – volume: 32 start-page: 211 issn: 0021-5031 year: 1962 ident: 18 publication-title: Jpn. J. Exp. Med. – volume: 75 start-page: 2311 issn: 0022-1317 issue: 9 year: 1994 ident: 38 publication-title: J. Gen. Virol. doi: 10.1099/0022-1317-75-9-2311 – volume: 206 start-page: 324 issn: 0042-6822 issue: 1 year: 1995 ident: 4 publication-title: Virology doi: 10.1016/S0042-6822(95)80048-4 – volume: 115 start-page: 97 issn: 0042-6822 issue: 1 year: 1981 ident: 14 publication-title: Virology doi: 10.1016/0042-6822(81)90092-1 – volume: 181 start-page: 1 issn: 0022-2836 issue: 1 year: 1985 ident: 24 publication-title: J. Mol. Biol. doi: 10.1016/0022-2836(85)90320-1 – ident: 37 doi: 10.1016/0042-6822(92)90706-U – ident: 42 doi: 10.1006/viro.1995.1202 – volume: 9 start-page: 283 issn: 0091-0279 year: 1993 ident: 31 publication-title: Vet. Clin. North Am. – ident: 41 doi: 10.1016/0264-410X(95)00080-K – ident: 7 doi: 10.1016/0042-6822(92)91200-E – volume: 67 start-page: 3961 issn: 0022-538X issue: 7 year: 1993 ident: 13 publication-title: J. Virol. doi: 10.1128/JVI.67.7.3961-3968.1993 |
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Snippet | The nucleotide sequences of the glycoprotein I (gI) and E (gE) genes of equine herpesvirus type 4 (EHV-4) strain TH20 were determined. The predicted region... |
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SubjectTerms | Amino Acid Sequence Animals Base Sequence CABALLOS Cells, Cultured CHEVAL EQUINE HERPESVIRUS equine herpesvirus type 4 GENE GENES Genome, Viral GLICOPROTEINAS glycoprotein E glycoprotein I GLYCOPROTEINE GLYCOPROTEINS HERPESVIRUS EQUIN HERPESVIRUS EQUINO HORSES Kidney Molecular Sequence Data NUCLEOTIDE SEQUENCE Open Reading Frames Restriction Mapping SECUENCIA NUCLEOTIDICA Sequence Alignment Sequence Homology, Amino Acid SEQUENCE NUCLEOTIDIQUE Varicellovirus - genetics Varicellovirus - physiology Viral Envelope Proteins - biosynthesis Viral Envelope Proteins - chemistry Viral Envelope Proteins - genetics |
Title | Nucleotide sequences of glycoprotein I and E genes of equine herpesvirus type 4 |
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