| Project/Area Number |
04807020
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| Research Category |
Grant-in-Aid for General Scientific Research (C)
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| Allocation Type | Single-year Grants |
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| Research Field |
Pathological medical chemistry
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| Research Institution | University of the Ryukyus |
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Principal Investigator |
TOKU Seikichi University of the Ryukyus, Biochemistry, instructor, 医学部, 助手 (10143091)
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| Co-Investigator(Kenkyū-buntansha) |
MAEDA Noriko University of the Ryukyus, Biochemistry, instructor, 医学部, 教務職員 (40231584)
TANAKA Tatsuo University of the Ryukyus, Biochemistry, Professor, 医学部, 教授 (70018688)
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| Project Period (FY) |
1992 – 1993
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| Project Status |
Completed (Fiscal Year 1993)
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| Budget Amount *help |
¥1,700,000 (Direct Cost: ¥1,700,000)
Fiscal Year 1993: ¥400,000 (Direct Cost: ¥400,000)
Fiscal Year 1992: ¥1,300,000 (Direct Cost: ¥1,300,000)
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| Keywords | ribosomal protein L37a / ribosomal protein L7a / coordinate expression / carcinogenesis / oncogene / Ets oncoprotein / リボソーム蛋白 L37a / リボソーム蛋白質 / L7a / L37a / L5 / L30 / プロモーター / 転写因子 / ETS |
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| Research Abstract |
To reveal gene expression of ribosomal proteins and its regulation by oncoproteins, we characterized gene promoters of chicken ribosomal protein L7a and L37a in terms of cis-elements for nuclear protein binding and for transcriptional regulation. The promoter of L37a had seven protein binding regions (designated from upstream as A to G). Regions B contained two Ets oncoprotein binding sites (EBS), and its deletion resulted in drastic loss of promoter activity. Cooperation of both EBS for protein binding and promoter activity was observed. EMSA analysis of region C encompassing transcription initiation site revealed binding of a factor differing from TBP.Region D containing a sequence homologous to delta factor-binding element of mouse L32 gene located at the junction between exon I and intron I.Deletion of the region increased promoter activity about 5 folds, indicating repressive function reversed to the mouse element. Regions E to G constituted internal control region in the intron I.Moreover, we found quite similarities in sequence and in the position of regions, B, C, D, E and G among various r-protein gene promoters. It could be probable that these common elements are involved in the coordinate expression of r-protein genes, and that the non coordinate expression is caused by abnormality of oncoprotein such as Ets proteins.
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