| Project/Area Number |
02808051
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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 |
分子遺伝学・分子生理学
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| Research Institution | Saitama Medical School (1991)
Okazaki National Research Institutes (1990) |
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Principal Investigator |
TAMURA Taka-aki Saitama Medical School, Faculty of Medicine, Associate Professor, 医学部, 助教授 (30112692)
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| Project Period (FY) |
1990 – 1991
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| Project Status |
Completed (Fiscal Year 1991)
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| Budget Amount *help |
¥1,600,000 (Direct Cost: ¥1,600,000)
Fiscal Year 1991: ¥500,000 (Direct Cost: ¥500,000)
Fiscal Year 1990: ¥1,100,000 (Direct Cost: ¥1,100,000)
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| Keywords | Transcription factor / Transcriptional regulation |
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| Research Abstract |
The core promoter of the mouse myelin basic protein (MBP) gene from -36 to +12 was tissue-specifically (brain) transcribed. Biochemical studies demonstrated that TFIID fraction contains factors involved in such a specific transcription. Tnus. we hypothesized the existence of a tissuespecific TFIID. We isolated a cDNA clone for TFIID from the mouse brain, and compared its structure with the human TFIID. Few minor differences were observed only in the N-terminal portion of the mouse TFIID. The C-terminus that is required for the TFIID function was identical among two TFIIDs. Only a single TFIID gene was detected in mouse genome. Northern blot analysis demonstated that the TFIID transcript is expressedas the same size RNAs in mouse tissues. Mutation analysis within the MBP core promoter showed that the TATA-box is not essential but TATA-flanking sequences were important for tissue-specific transcription. From these results, there may be no tissue-specific TFIID. In these days, TFIID associating factors (TAF) have been identified by other groups. In our case, it is suggested that a tissue-specific TAF can be involved in the core promoter-mediated tissue-specific transcription.
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