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2000 Fiscal Year Final Research Report Summary

Molecular Mechanism of Epstein-Barr virus DNA replication in viral infected tumors and cellular immunity for viral associated cancers

Research Project

Project/Area Number 11138268
Research Category

Grant-in-Aid for Scientific Research on Priority Areas (A)

Allocation TypeSingle-year Grants
Research InstitutionAichi Cancer Center Research Institute

Principal Investigator

TSURUMI Tatsuya  Aichi Cancer Center, Division of Virulogy, Chief, ウイルス部, 部長 (90172072)

Co-Investigator(Kenkyū-buntansha) YOKOYAMA Naoaki  Aichi Cancer Center, Division of Virulogy, Researcher, ウイルス部, 研究員 (80301802)
FUJITA Masatoshi  Aichi Cancer Center, Division of Virulogy, Senior Researcher, ウイルス部, 主任研究員 (30270713)
KUZUSHIMA Kiyotaka  Aichi Cancer Center, Division of Virulogy, Section Head, ウイルス部, 室長 (30311442)
Project Period (FY) 1999
KeywordsDNA replication / Epstein-Barr virus / helicase / primase / protein-protein interaction / MCM / CDC6
Research Abstract

EBV encodes seven viral genes that are essential for the oriLyt-dependent DNA replication. The BZLF1 protein is an oriLyt-binding protein and acts also the lytic transactivator. The BALF5 gene encodes the DNA Pol catalytic subunit and the BMRF1 gene encodes the DNA Pol accessory subunit. A single-stranded DNA-binding protein is encoded by the BALF2 gene . The functions of the remaining three proteins encoded by the genes BBLF4 , BSLF1, and BBLF2/3 are not demonstrated but predicted to be helicase, primase, and helicase-primase associated proteins, respectively. In the present study, we found that the EBV DNA Pol catalytic subunit interacts with the BBLF4/BSLF1/BBLF2/3 complex by immunoprecipitation analyses. The interactions of the EBV DNA polymerase with the EBV putative helicase-primase complex warrant particular attention because they are thought to coordinate leading and lagging strand DNA synthesis at the replication fork.
We have been also studying cell cycle regulation of latent … More phase EBV DNA replication, focusing on hORC, hCDC6 and hMCM proteins, all of which are thought to be key regulators of initiation of DNA replication. Current model which we hypothesize from our and others data is as follows. ORC and CDC6 are assumed to be associated with the matrix throughout the cell cycle. MCM heterohexameric complexes are loaded, by ORC/CDC6, mainly onto chromatin regions not associated with the matrix. The abundance of chromatin-bound MCM is several times that of bound CDC6, and the relatively large extent of MCM-bound chromatin could explain the pattern of initiation in mammalian cells, namely the so-called "initiation zone". The bound MCMs might be activated through phosphorylation possibly by CDC7 and CDK2 kinase. The activated MCM plays an unknown but essential role in DNA replication, and is simultaneously displaced from chromatin, coupled to DNA replication.
Gastric adenocarcinomas carrying EBV are known to be accompanied by massive lymphocyte infiltration. To characterize the tumor infiltrating lymphocytes(TILs), we isolated and cultured such cells from surgically resected EBV-associated gastric carcinoma. The isolated TILs consisted of HLA-class I-restricted CD8+ cytotoxic T lymphocytes(CTLs) which killed autologous EBV-transformed cells but not PHA blast cells and recognized HLA-A24 as restriction molecules. Our data indicated that some cellular proteins may be involved in the strong T cell response to EBV-associated gastric carcinoma. Less

  • Research Products

    (18 results)

All Other

All Publications (18 results)

  • [Publications] Kuzushima K. et al.: "Increased frequency of antigen-specific CD8^+ cytotoxic T lympheytes intiltrcting an Epstein-Barr virus-associated gastric carcinoma."J.Clin.Invest.. 104. 163-171 (1999)

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      「研究成果報告書概要(和文)」より
  • [Publications] Fujita M. et al.: "Cell cycle regulation at of human CDC6 protain : intruicallularv lccaligationy intoraction with the human MCM complex and cde2 kinsse-mediated hyperphosphonylation"J.Biol.Chem.. 274. 25927-25932 (1999)

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      「研究成果報告書概要(和文)」より
  • [Publications] Yokoyama N. et al.: "Assonbly of the Epstain-Barr virus BBLF4, BSLF1, and BBLF2/3 proteins and their interactive properties"J.Gen.Virol.. 80. 2879-2887 (1999)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Hoshiro Y. et al.: "Antigon-driven expansion and contraction of CD8^+ activated T cells in primary EBV infection"J.Immunol.. 163. 5735-5740 (1999)

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      「研究成果報告書概要(和文)」より
  • [Publications] Kuzushima K et al.: "Rapid detormination of Epstain-Barr virus-spoific CD8^+ T cell freguencies by flow cytometry"Blood. 94. 3094-3100 (1999)

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      「研究成果報告書概要(和文)」より
  • [Publications] Fujii K. et al.: "The Epstein-Barr virus Pol catalytic subunit physically interacts with the BBLF4-BSLF1-BBLF2/3 complex"J.Virol. (in press). (2000)

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      「研究成果報告書概要(和文)」より
  • [Publications] 鶴見達也: "微生物学:ヘルペスウイルス"文光堂(畑中正一,嶋田甚五郎 編集). 187-199 (1999)

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      「研究成果報告書概要(和文)」より
  • [Publications] Tsurumi,T.: "Curr.Top.Microbiology.Immunol.: EBV replication engymes"Springer-Verlag Gmb H & Co.kG. (in press). (2000)

    • Description
      「研究成果報告書概要(和文)」より
  • [Publications] Kuzushima, K, Nakamura S., Nakamura T., Yamamura Y., Yokoyama N., Fujita M., Kiyono T., and Tsurumi T.: "Increased frequency of antigen-specific CD8+ cytotoxic T lymphocytes infiltrating an Epstein-Barr virus-associated gastric carcinoma."J.Clin.Invest.. 104. 163-171 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kuzushima, K, Hoshino Y., Fujii K., Yokoyama N., Fujita M., Kiyono T., Kimura H., Morishima T., Morishima Y.and Tsurumi T.: "Rapid determination of Epstein-Barr virus-specific CD8+T cell frequencies by flow cytometry"Boold. 94. 3094-3100 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Fujita, M., Yamada C., Goto H., Yokoyama N., Kuzushima K., Inagaki M., and Tsurumi T.: "Cell cycle regulataion of human CDC6 protein : intracellular localization, interaction with the human MCM complex and cdc2 kinase-mediated hyperphosphorylation."J.Biol.Chem.. 274. 25927-25932 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Yokoyama N., Fujii K., Hirata M., Tamai K., Kiyono T., Kuzushima K., Nishiyama Y, Fujita M, and Tsurumi T.: "Assembly of the Epstein-Barr Virus BBLF4, BSLF1, and BBLF2/3 Proteins and Their Interactive Properties."J.Gen.Virol.. 80. 2879-2887 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Hoshino Y., Morishima T., Kimura H., Nishikawa K., Tsurumi T., and Kuzushima K.: "Antigen-driven expansion and contraction of CD8+ activated T cells in primary EBV infection."J.Immunol.. 163. 5735-5740 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Fujii K., Yokoyama, N., KiyonoT., Kuzushima K., Honma M., Nishiyama Y., Fujita M., and Tsurumi T.: "The Epstein-Barr virus Pol catalytic subunit physically interacts with the BBLF4-BSLF1-BBLF2/3 complex."J.Virol.. (in press).

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Kuzushima K., Kimura H., Hoshino Y., Morishima T., Tsuge I., Horibe K., Tsurumi T.and Kojima S.: "Massive expansion and subsequent contraction of Epstein-Barr virus-specific CD8+ cytotoxic T lymphocytes during regression of post-transplant lymphoproliferative disorder."Blood. (in press).

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      「研究成果報告書概要(欧文)」より
  • [Publications] Yokoyama, N., Hirata M., Ohtsuka K., Fujii K., Fujita M., Kuzushima K., Kiyono T., and Tsurumi T.: "Co-expression of human chaperone Hsp70 and Hsdj and Hsp40 Co-factor increases solubility of overexpressed target proteins in insect cells."FEBS lett.. (in press).

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      「研究成果報告書概要(欧文)」より
  • [Publications] Tsurumi T.: "Herpesviruses "Microbiology" : (edited by Hatanaka M and Shimada J)"Bunnkodo Co.. 187-199 (1999)

    • Description
      「研究成果報告書概要(欧文)」より
  • [Publications] Tsurumi T.: "EBV replication enzymes Curr.Top.Microbiol.Immunol."Springer-Verlay, GmbH&Co.KG.(in press).

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      「研究成果報告書概要(欧文)」より

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Published: 2002-03-26  

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