Identification of the Marek's disease virus serotype 2 genes homologous to the glycoprotein B (UL27), ICP18.5 (UL28) and major DNA-binding protein (UL29) genes of herpes simplex virus type 1

We determined the nucleotide sequence of non-pathogenic Marek's disease virus serotype 2 (MDV2) strain HPRS24 glycoprotein B (gB) (UL27), ICP18.5 (UL28) and major DNA-binding protein (MDBP) (UL29) genes homologous to herpes simplex virus type 1 (HSV-1). The sequence data revealed that important...

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Published inJournal of Veterinary Medical Science Vol. 61; no. 10; pp. 1161 - 1165
Main Authors Kato, K. (Tokyo Univ. (Japan). Faculty of Agriculture), Jang, H.K, Izumiya, Y, Cai, J.S, Tsushima, Y, Miyazawa, T, Kai, C, Mikami, T
Format Journal Article
LanguageEnglish
Published Japan JAPANESE SOCIETY OF VETERINARY SCIENCE 01.10.1999
Japan Science and Technology Agency
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ISSN0916-7250
1347-7439
DOI10.1292/jvms.61.1161

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Abstract We determined the nucleotide sequence of non-pathogenic Marek's disease virus serotype 2 (MDV2) strain HPRS24 glycoprotein B (gB) (UL27), ICP18.5 (UL28) and major DNA-binding protein (MDBP) (UL29) genes homologous to herpes simplex virus type 1 (HSV-1). The sequence data revealed that important motives in the proteins are conserved in MDV2 ICP18.5 and MDBP, however the sequence of viral DNA replication origin which exists in the regions between the UL29 and UL30 genes of other alphaherpesviruses was not found in the regions of the MDV2 genome. By northern blot analyses, we also demonstrated that 8.9, 5.0 and 2.6 kb transcripts were actually transcribed from the sequenced region in MDV2-infected cells. The MDV2 UL28 and UL29 genes have not been reported in other serotypes of MDV
AbstractList We determined the nucleotide sequence of non-pathogenic Marek's disease virus serotype 2 (MDV2) strain HPRS24 glycoprotein B (gB) (UL27), ICP18.5 (UL28) and major DNA-binding protein (MDBP) (UL29) genes homologous to herpes simplex virus type 1 (HSV-1). The sequence data revealed that important motives in the proteins are conserved in MDV2 ICP18.5 and MDBP, however the sequence of viral DNA replication origin which exists in the regions between the UL29 and UL30 genes of other alphaherpesviruses was not found in the regions of the MDV2 genome. By northern blot analyses, we also demonstrated that 8.9, 5.0 and 2.6 kb transcripts were actually transcribed from the sequenced region in MDV2-infected cells. The MDV2 UL28 and UL29 genes have not been reported in other serotypes of MDV.
We determined the nucleotide sequence of non-pathogenic Marek's disease virus serotype 2 (MDV2) strain HPRS24 glycoprotein B (gB) (UL27), ICP18.5 (UL28) and major DNA-binding protein (MDBP) (UL29) genes homologous to herpes simplex virus type 1 (HSV-1). The sequence data revealed that important motives in the proteins are conserved in MDV2 ICP18.5 and MDBP, however the sequence of viral DNA replication origin which exists in the regions between the UL29 and UL30 genes of other alphaherpesviruses was not found in the regions of the MDV2 genome. By northern blot analyses, we also demonstrated that 8.9, 5.0 and 2.6 kb transcripts were actually transcribed from the sequenced region in MDV2-infected cells. The MDV2 UL28 and UL29 genes have not been reported in other serotypes of MDV
We determined the nucleotide sequence of non-pathogenic Marek's disease virus serotype 2 (MDV2) strain HPRS24 glycoprotein B (gB) (UL27), ICP18.5 (UL28) and major DNA-binding protein (MDBP) (UL29) genes homologous to herpes simplex virus type 1 (HSV-1). The sequence data revealed that important motives in the proteins are conserved in MDV2 ICP18.5 and MDBP, however the sequence of viral DNA replication origin which exists in the regions between the UL29 and UL30 genes of other alphaherpesviruses was not found in the regions of the MDV2 genome. By northern blot analyses, we also demonstrated that 8.9, 5.0 and 2.6 kb transcripts were actually transcribed from the sequenced region in MDV2-infected cells. The MDV2 UL28 and UL29 genes have not been reported in other serotypes of MDV.We determined the nucleotide sequence of non-pathogenic Marek's disease virus serotype 2 (MDV2) strain HPRS24 glycoprotein B (gB) (UL27), ICP18.5 (UL28) and major DNA-binding protein (MDBP) (UL29) genes homologous to herpes simplex virus type 1 (HSV-1). The sequence data revealed that important motives in the proteins are conserved in MDV2 ICP18.5 and MDBP, however the sequence of viral DNA replication origin which exists in the regions between the UL29 and UL30 genes of other alphaherpesviruses was not found in the regions of the MDV2 genome. By northern blot analyses, we also demonstrated that 8.9, 5.0 and 2.6 kb transcripts were actually transcribed from the sequenced region in MDV2-infected cells. The MDV2 UL28 and UL29 genes have not been reported in other serotypes of MDV.
Author Miyazawa, T
Mikami, T
Kato, K. (Tokyo Univ. (Japan). Faculty of Agriculture)
Cai, J.S
Jang, H.K
Tsushima, Y
Izumiya, Y
Kai, C
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References_xml – reference: 13) Jang, H.-K., Niikura, M., Song, C.-S. and Mikami, T. 1997. Virus Res. 48: 111-123.
– reference: 23) Pederson, N. E. and Enquist, L. W. 1989. Nucleic Acids Res. 17: 3597.
– reference: 1) Addison, C., Rixon, F. J., Palfreyman, J. W., O’Hara, M. and Preston, V. G. 1984. Virology 138: 246-259.
– reference: 12) Izumiya, Y., Jang, H. K., Kashiwase, H., Cai, J. S., Nishimura, Y., Tsushima, Y., Kato, K., Miyazawa, T., Kai, C. and Mikami, T. 1998. J. Gen. Virol. 79: 1997-2001.
– reference: 8) Hardwicke, M. A. and Schaffer, P. A. 1995. J. Virol. 69: 1377-1388.
– reference: 5) Chee, M. S., Bankier, A. T., Beck, S., Bohni, R., Brown, C. M., Cerny, R., Horsnell, T., Hutchison III, C. A., Kouzarides, T., Martignetti, J. A., Preddie, E., Satchwell, S. C., Tomlinson, P., Weston, K. M. and Barrell, B. G. 1990. Curr. Top Microbiol. Immunol. 154: 125-169.
– reference: 6) Davison, A. J. and Scott, J. E. 1986. J. Gen. Virol. 67: 1759-1816.
– reference: 4) Buckmaster, A. E., Scott, S. D., Sanderson, M. J., Boursnell, M. E. G., Ross, L. J. N. and Binns, M. M. 1988. J. Gen. Virol. 69: 2033-2042.
– reference: 18) Lukonis, C. J., Burkham, J. and Weller, S. K. 1997. J. Virol. 71: 4771-4781.
– reference: 27) Schwyzer, M. and Ackermann, M. 1996. Vet. Micro. 53: 17-29.
– reference: 16) Kato, K., Jang, H.-K., Izumiya, Y., Cai, J.-S., Tsushima, Y., Miyazawa, T., Kai, C. and Mikami, T. 1999. J. Vet. Med. Sci. 61: 787-793.
– reference: 30) Silva, R. F. and Barnett, J. C. 1991. Avian Dis. 35: 487-495.
– reference: 14) Jang, H.-K., Ono, M., Kim, T.-J., Cai, J.-S., Tsushima, Y., Niikura, M. and Mikami, T. 1996. J. Vet. Med. Sci. 58: 1057-1066.
– reference: 28) Shimojima, Y., Jang, H.-K., Ono, M., Kai, C. and Mikami, T. 1997. J. Vet. Med. Sci. 59: 629-634.
– reference: 31) Telford, E. A., Watson, M. S., McBride, K. and Davison, A. J. 1992. Virology 189: 304-316.
– reference: 15) Jang, H.-K., Ono, M., Kato, Y., Tohya, Y., Niikura, M. and Mikami, T. 1996. Arch. Virol. 141: 2207-2216.
– reference: 34) Yoshida, S., Lee, L. F., Yaragida, N. and Nazerian, K. 1994. Virology 200: 484-493.
– reference: 26) Ross, L. J. N., Sanderson, M., Scott, S. D., Binns, M. M., Doel, T. and Milne, B. 1989. J. Gen. Virol. 70: 1789-1804.
– reference: 33) Wang, Y. and Hall, J. D. 1990. J. Virol. 64: 2082-2089.
– reference: 10) Hirai, K., Nakajima, K., Ikuta, K., Kirisawa, R., Kawakami, Y., Mikami, T. and Kato, S. 1986. Arch. Virol. 89: 113-130.
– reference: 32) Tengelsen, L. A., Pederson, N. E., Shaver, P. R., Wathen, M. W. and Homa, F. L. 1993. J. Virol. 67: 3470-3480.
– reference: 9) Hirai, K., Ikuta, K., Maotani, K. and Kato, S. 1984. J. Biochem. (Tokyo) 95: 1215-1218.
– reference: 24) Pederson, N. E. and Enquist, L.W. 1991. J. Virol. 65: 3746-3758.
– reference: 3) Baer, R. J., Bankier, A. T., Biggin, M. D., Deininger, P. L., Farrell, P. J., Gibson, T. J., Hatfull, G. F., Hudson, G. S., Satchwell, S. C., Seguin, C., Tuffnell, P. S. and Barrell, B. G. 1984. Nature (Lond.) 310: 207-211.
– reference: 7) Gupte, S. S., Olsen, J. W. and Ruyechan, W. T. 1991. J. Bio. Chem. 266: 11413-11416.
– reference: 20) Meyer, G., Vlcek, C., Paces, V., O’Hara, M. K., Pastoret, P.-P., Thiry, E. and Schwyzer, M. 1997. Arch. Virol. 142: 89-102.
– reference: 25) Ross, L. J. N., Milne, B. and Biggs, P. M. 1983. J. Gen. Virol. 64: 2785-2790.
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Snippet We determined the nucleotide sequence of non-pathogenic Marek's disease virus serotype 2 (MDV2) strain HPRS24 glycoprotein B (gB) (UL27), ICP18.5 (UL28) and...
We determined the nucleotide sequence of non-pathogenic Marek’s disease virus serotype 2 (MDV2) strain HPRS24 glycoprotein B (gB) (UL27), ICP18.5 (UL28) and...
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SubjectTerms ADN
Amino Acid Sequence
Animals
BINDING PROTEINS
Blotting, Northern
CHICKENS
Consensus Sequence
DNA
DNA Probes - chemistry
Electrophoresis, Agar Gel
GENE
Gene Library
GENES
GLICOPROTEINAS
GLYCOPROTEINE
GLYCOPROTEINS
Herpes simplex virus 1
Herpesvirus 1, Human - chemistry
Herpesvirus 1, Human - genetics
Herpesvirus 2, Gallid - chemistry
Herpesvirus 2, Gallid - genetics
HERPETOVIRIDAE
Marek Disease - genetics
Marek's disease herpesvirus
MAREK'S DISEASE VIRUS
Marek’s disease virus serotype 2
Molecular Sequence Data
POLLO
POULET
PROTEINAS AGLUTINANTES
PROTEINE DE LIAISON
RNA, Viral - isolation & purification
Sequence Alignment
Sequence Analysis, DNA
Sequence Homology, Amino Acid
UL27-UL29
VIRUS ENFERMEDAD DE MAREK
VIRUS MALADIE DE MAREK
Title Identification of the Marek's disease virus serotype 2 genes homologous to the glycoprotein B (UL27), ICP18.5 (UL28) and major DNA-binding protein (UL29) genes of herpes simplex virus type 1
URI https://www.jstage.jst.go.jp/article/jvms/61/10/61_10_1161/_article/-char/en
https://www.ncbi.nlm.nih.gov/pubmed/10563297
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Volume 61
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