1997 Fiscal Year Final Research Report Summary
Study of Pneumocystis carinii : from Molecular Microbiology to Drug Discovery
| Project/Area Number |
07557027
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (A)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 展開研究 |
|---|
| Research Field |
Bacteriology (including Mycology)
|
|---|
| Research Institution | The University of Tokyo |
|---|
Principal Investigator |
NAKAMURA Yoshikazu The University of Tokyo Instiute of Medical Science, Associate Professor, 医科学研究所, 助教授 (40114590)
|
|---|
| Project Period (FY) |
1995 – 1997
|
| Keywords | AIDS / pneumonia / Pneumocystis carinii / antigenic variation / major surface glycoprotein / telomere / expression switch / subtilisin-like protease |
|---|
| Research Abstract |
The major cell surface glycoprotein (MSG) of Pneumocystis carinii plays a crucial role in the host-parasite interaction. We have discovered that genes encoding MSGs are repeated, highly polymorphic, distributed among all of the 14-15 chromosomes, and are expressed from a unique expression site termed UCS,leading to antigenic variation to evade the host immune system. We have shown further that a UCS site is telomeric and that antigenic variation may be generated by site-specific or homologous recombination between the UCS site and multiple MSG repertoires. Telomeric fragments other than the UCS were cloned by screening with the telomere sequence. Non-UCS telomeric clones that were sequenced also contained MSG gene (s) regardless of having been screened with non-MSG probes. Frequent occurrences of these telomeric MSG clones indicate that they represent silent MSG repertoires localized in the telomere regions. The UCS contained the two transcription start sites. The promoter activity of UCS was examined using a UCS-lacZ (beta-galactosidase gene) fusion in the budding yeast Saccharomyces cerevisiae and the fission yeast Shizosaccharomyces pombe because P.carinii is phylogenically close to yeast. UCS allowed beta-galactosidase synthesis in S.pombe but not in S.cerevisiae. The transcript start sites determined by 5'RACE analysis are located slightly upstream of the two authentic start sites in P.carinii. The promoter activity of UCS itself is about one fifth of that of a widely used promoter of S.pombe, nmtl. Three other putative promoter sequences of P.carinii also expressed a reporter gene in S.pombe. These findings indicate that Shizosaccharomyces pombe is useful as a heterologous expression host for native Pneumocystis carinii genes.
|
Research Products
(21 results)
-
[Publications] Mita, K., Morimyo, M., Ito, K., Sugano, K., Ebihara, K., Hongo, E., Higashi, T., Hirayama, Y., Nakamura, Y.: "Comprehensive cloning of Schizosaccharamyces pombe genes encoding translation elongation factors." Gene. 187. 259-266 (1997)
Description
「研究成果報告書概要(和文)」より
-
-
-
-
-
-
-
-
[Publications] Desgupta, S., Fernandez, L., Kameyama, L., Inada, T., Nakamura, Y., Pappas, A., Court, D: "Genetic uncoupling of the dsRNA-binding and RNA-cleavage activities of the Escherichia coli endoribonuclease RNaseIII-the effect of dsRNA binding on gene expression." Mol.Microbiol.(In press). (1998)
Description
「研究成果報告書概要(和文)」より
-
-
[Publications] Yasuoka, A., Oka, S., Komuro, K., Shimizu, H., Kitada, K., Nakamura, Y., Shibahara, S., Takeuchi, T., Kondo, S., Shimada, K., Kimura, S.: "Successful treatment of Pneumocystis carinii pneumonia in mice with benanomicin A (ME1451)" Antimicro.Agent.Chemother.39. 720-724 (1995)
Description
「研究成果報告書概要(欧文)」より
-
-
-
-
-
[Publications] Mita, K., Morimyo, M., Ito, K., Sugano, K., Ebihara, K., Hongo, E., Higashi, T., Hirayama, Y., Nakamura, Y.: "Comprehensive cloning of Schizosaccharamyces pombe genes encoding translation elongation factors." Gene. 187. 259-266 (1997)
Description
「研究成果報告書概要(欧文)」より
-
-
-
-
-
