Skip to main content
Log in

Study on the structure of heteropolymer pp38/pp24 and its enhancement on the bi-directional promoter upstream of pp38 gene in Marek’s disease virus

  • Article
  • Published:
Science in China Series C: Life Sciences Aims and scope Submit manuscript

Abstract

In the latest report, Chloramphenicol acetyltransferase (CAT) gene was used as a reporter to investigate the influence of pp38 on its upstream bi-directional promoter, and it was found that the co-expression of pp38 and pp24 can significantly enhance the transactivity of the bi-directional promoter between pp38 gene and 1.8-kb mRNA transcript in genome of Marek’s disease virus (MDV). In this study, enhanced green fluorescence protein (EGFP) gene was used as another reporter to further investigate the promoter activity. The transfection shows the promoter has the complete activity under the condition of co-expression of pp38 and pp24 in the same cells. Immunoprecipitation test was used to verify the structure of pp38/pp24 heteropolymer. The pp38-specific monoclonal antibody H19 was used in this test, and pp38, pp24 or both were prepared from the pcDNA-pp38, pcDNA-pp24 or pBud-pp38-pp24 transfected chicken embryonic fibroblast (CEF), respectively. Immunoprecipitation indicates that pp24 could be co-precipitated with pp38 by MabH19, implying that pp24 and pp38 were able to form a heteropolymer in the natural condition. The two separated tests clarify that pp38 and pp24 form a heteropolymer, which enhances the activity of the promoter.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Ikuta K, Nishi Y, Kato S, et al. Identification of Marek’s disease virus-specific antigens in Marek’s disease lymphobastoid cell lines using monoclonal antibody against virus-specific phosphorylated polypeptides. Int J Cancer, 1985, 35: 257–264, 2982746, 10.1002/ijc.2910350219, 1:STN:280:BiqC38bmsVw%3D

    Article  PubMed  CAS  Google Scholar 

  2. Nakajima K, Ikuta K, Naito M., et al. Analysis of Marek’s disease virus-specific phosphorylated polypeptides in virus-infected cells and Marek’s disease lymphoblastoid cells. J Gen Virol, 1987, 68:1379–1389, 3033141, 10.1099/0022-1317-68-5-1379, 1:CAS:528:DyaL2sXkt1Sntro%3D

    Article  PubMed  CAS  Google Scholar 

  3. Camp H S, Coussens P M, Silva R F. Cloning, sequencing, and functional analysis of a Marek’s disease virus origin of DNA replication. J Virol, 1991, 65: 6320–6324, 1656099, 1:CAS:528:DyaK3MXmslWrtrs%3D

    PubMed Central  PubMed  CAS  Google Scholar 

  4. Endoh D, Niikura M, Hirai K, et al. Expression and purification of recombinant Marek’s disease virus serotype 1specific phosphated protein pp38 in E. coli. J Vet Med Sci, 1994, 56: 823–826, 7865579, 1:CAS:528:DyaK2MXit1entb4%3D

    Article  PubMed  CAS  Google Scholar 

  5. Liu J L, Lin S F, Xia L, et al. MEQ and V-IL8: Cellular genes in disguise? Acta Virol, 1999, 43: 94–101, 10696427, 1:CAS:528:DyaK1MXltVWls7o%3D

    PubMed  CAS  Google Scholar 

  6. Liu J L, Ye Y, Lee L F, et al. Transforming potential of the herpesvirus oncoprotein MEQ: Morphological transformation, serum-independent growth, and inhibition of apoptosis. J Virol, 1998, 72: 388–395, 9420237, 1:CAS:528:DyaK1cXhvVGnsA%3D%3D

    PubMed Central  PubMed  CAS  Google Scholar 

  7. Ding J B, Cui Z Z, Lee L F, et al. The role of pp38 in regulation of Marek’s disease virus bi-directional promoter between pp38 and 1.8-kb mRNA. Virus Genes, 2006, 32: 193–201, 16604452, 10.1007/s11262-005-6876-2, 1:CAS:528:DC%2BD28Xjt1yktbo%3D

    Article  PubMed  CAS  Google Scholar 

  8. Ding J B, Cui Z Z, Jiang S J, et al. The enhancement effect of pp38 gene product on the activity of its upstream bi-directional promoter in Marek’s disease virus. Sci China Ser C-Life Sci, 2006, 49: 153–162

    Google Scholar 

  9. Silva R F, Lee L F. Monoclonal antibody mediated immunoprecipitation of proteins from cells infected with Marek’s disease virus or turkey herpes virus. Virology, 1984, 136: 307–320, 6205501, 10.1016/0042-6822(84)90167-3, 1:CAS:528:DyaL2cXlt1Knur4%3D

    Article  PubMed  CAS  Google Scholar 

  10. Zhu G S, Iwata A, Gong M, et al. Marek’s disease virus type 1-specific phosphorylated protein pp38 and pp24 with common amino acid termini are ecoded from the opposite junction regions between the long unique and inverted repeat sequences of viral genome. Virology, 1994, 200: 816–820, 8178465, 10.1006/viro.1994.1249, 1:CAS:528:DyaK2cXkslCrtrc%3D

    Article  PubMed  CAS  Google Scholar 

  11. Cui Z, Qin A, Lee L F, et al. Construction and characterization of a H19 epitope point mutant of MDV CVI988/Rispens strain. Acta Virol, 1999, 43: 169–173, 10696440, 1:CAS:528:DyaK1MXltVWlsL0%3D

    PubMed  CAS  Google Scholar 

  12. Ding J B, Cui Z Z, Lee L F. Marek’s disease virus unique genes pp38 and pp24 are essential for transactivating the bi-directional promoters for the 1.8-kb mRNA transcripts. Virus Genes, 2007, 35(3): 643–650, 17619133, 10.1007/s11262-007-0129-5, 1:CAS:528:DC%2BD2sXht1ags7fE

    Article  PubMed  CAS  Google Scholar 

  13. Lee L F, Liu X, Witter R L. Monoclonal antibodies with specificity for three different serotypes of Marek’s disease viruses in chickens. J Immunol, 1983, 130: 1003–1006, 6184394, 1:STN:280:BiyD1czpt1w%3D

    PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to ZhiZhong Cui.

Additional information

Contributed equally to this work

Supported by the National Natural Science Foundation of China (Grant Nos. 30700596 and 30070544)

Rights and permissions

Reprints and permissions

About this article

Cite this article

Ding, J., Cui, Z., Jiang, S. et al. Study on the structure of heteropolymer pp38/pp24 and its enhancement on the bi-directional promoter upstream of pp38 gene in Marek’s disease virus. SCI CHINA SER C 51, 821–826 (2008). https://doi.org/10.1007/s11427-008-0099-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11427-008-0099-4

Keywords

Navigation