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ANALYSIS OF TWO PROMOTERS AND 5'FLANKING REGION OF RAT SERINE : PYRUVATE AMINOTRANSFERASE GENE

ANALYSIS OF TWO PROMOTERS AND 5'FLANKING REGION OF RAT SERINE : PYRUVATE AMINOTRANSFERASE GENE
大鼠丝氨酸丙酮酸转氨酶基因的两个启动子和5侧翼区的分析
批准号:
05680546
负责人:
ODA Toshiaki
金额:
$1.28万
依托单位国家:
日本
项目类别:
Grant-in-Aid for General Scientific Research (C)
财政年份:
1993
资助国家:
日本
项目状态:
已结题
起止时间:
1993 至 1994

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ODA Toshiaki的其他基金

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中文摘要
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英文摘要
(1) Sequence required for the basal transcriptional activity of two SPT gene promotersA single SPT gene has two promoters, the upstream promoter (transcribed from+1) which has TATA box and whose activity is enhanced by cAMP administration and the downstream promoter (transcribed from +66) which contains no TATA box and whose activity is not affected by cAMP.To identify the regions necessary for the basal transcription by these two promoters, I constructed many 5'-deleted recombinant plasmids whose 3'-ends are +36 for the upstream promoter or +106 for the downstream promoter. The transcription from the upstream initiation site was reached to a maximum level in a plasmid containing a sequence from -192 to +36 of SPT gane, suggesting that, in addition to CCAAT box and TATA box which are located between -103 and +36 ; some element (s) contained between -192 and -103 is necessary for the maximum activity. The transcriptional activity of the downstream promoter, on the other hand, was detect … More ed in a plasmid having a sequence from +36 to +106 and was reached to a maximum level in a plasmid containing a sequence from -51 to +106. This suggests that some element contained between -51 and +11 are necessary for the maximum transcriptional activity of the downstream promoter even if HIP1 (Housekeeping initiation protein 1), which is proposed as one of TATA-less promoters and is located between +11 and +106, functions as the downstream promoter.(2) Transcriptional regulation and cell-specific expression of SPT geneIt has been indicated that the region downstream from -103 contributes to the enhancement of SPT gene by cAMP rather than CRE (cAMP responsive element) located between -684 and -621. This enhancement was observed only in HepG2 cells, not in HeLa, CHO-K1, CV-1 and COS-1 cells. Because the transcriptional enhancement of SPT gene by cAMP is repressed by cycloheximide, a inhibitor of protein synthesis, it seems that CREB (CRE binding protein) first increases the liver-specific expression of some transcriptional factor and then the translation factor acts on the proximal region of SPT gene to cause the enhancement of SPT gene transcription. Less
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Oda,T: "Characterization and sequence analysis of rat serine:pyruvate/alanine:glyoxylate aminotransferase gene" Genomics. 17. 59-65 (1993)
Oda,T:“大鼠丝氨酸:丙酮酸/丙氨酸:乙醛酸转氨酶基因的表征和序列分析”基因组学。
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Uchida,C: "Regulation by glucagon of serine:pyruvate/alanine:glyoxylate aminotransferase gene expression in cultured rat hepatocytes" J.Biol.Chem.269. 8849-8856 (1994)
Uchida,C:“培养的大鼠肝细胞中丝氨酸:丙酮酸/丙氨酸:乙醛酸转氨酶基因表达的胰高血糖素调节”J.Biol.Chem.269。
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Ohbayashi,K.: "Characterization of transcription from the downstream start site of the rat serine:pyruvate/alanine:glyoxylato aminotransferase gone" Biomed.Res.(in press). (1995)
Ohbayashi,K.:“大鼠丝氨酸下游起始位点的转录特征:丙酮酸/丙氨酸:乙醛酸转氨酶消失”Biomed.Res.(正在出版)。
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Sato,S: "Quantitative cryoimmunogold electron microscopic studies on induction of serine:pyruvate aminotransferase in rat liver mitochondria by administration of glucagon" Cell Struct.Funct.(印刷中). (1995)
Sato, S:“通过施用胰高血糖素对大鼠肝线粒体中丝氨酸:丙酮酸转氨酶的诱导进行定量冷冻免疫金电子显微镜研究”Cell Struct.Funct(出版中)。
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12
    A comparative study on morphology and functions of muscle-tendon complex in Japanese and Kenyan distance runners
    • 批准号:
      23500729
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $3.33万
    • 财政年份:
      2011
    • 负责人:
      ODA Toshiaki
    • 依托单位:
    Determination of local stress and deformation in human skeletal muscles using a combined approach of in vivo experiments with computer simulation.
    Ubiquitination of overexpressed protein and enclosure by inducible ER membrane
    • 批准号:
      17590244
    • 项目类别:
      Grant-in-Aid for Scientific Research (C)
    • 资助金额:
      $2.24万
    • 财政年份:
      2005
    • 负责人:
      ODA Toshiaki
    • 依托单位:
    Analysis of mechanism for selective translocation of a protein having two subcellular localization signals
    • 批准号:
      10480165
    • 项目类别:
      Grant-in-Aid for Scientific Research (B)
    • 资助金额:
      $2.82万
    • 财政年份:
      1998
    • 负责人:
      ODA Toshiaki
    • 依托单位: