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mi基因座编码的转录因子对小鼠肥大细胞蛋白酶6基因表达的调控

Regulation of mouse mast cell protease 6 gene expression by transcription factor encoded by the mi locus.

作者信息

Morii E, Tsujimura T, Jippo T, Hashimoto K, Takebayashi K, Tsujino K, Nomura S, Yamamoto M, Kitamura Y

机构信息

Department of Pathology, Osaka University Medical School, Japan.

出版信息

Blood. 1996 Oct 1;88(7):2488-94.

PMID:8839840
Abstract

The mi locus of mice encodes a member of the basic-helix-loop-helix-leucine zipper (bHLH-Zip) protein family of transcription factors (hereafter called MITF). Because the expression of the mouse mast cell protease 6 (MMCP-6) gene is remarkably reduced in mast cells of mi/mi mutant mice, we investigated the effect of MITF on the transcription of the MMCP-6 gene. First, we introduced the normal (+) MITF cDNA into mi/mi cultured mast cells using the retroviral vector. Overexpression of +-MITF but not mi-MITF normalized the expression of the MMCP-6 gene, indicating the involvement of +-MITF in the MMCP-6 gene transactivation. Second, we analyzed the promoter of the MMCP-6 gene by the transient cotransfection assay. The luciferase construct under the control of the MMCP-6 promoter and the cDNA encoding +-MITF or mi-MITF were cotransfected into NIH/ 3T3 fibroblasts. The coexpression of +-MITF but not mi-MITF increased the luciferase activity 10-fold. We found a CACATG and a CATCTG motif in the MMCP-6 promoter, both of which are generally recognized by bHLH-Zip-type transcription factors. We also found a GACCTG motif that was strongly bound by +-MITF. These three motifs were necessary for the 10-fold transactivation ability of the MMCP-6 promoter by +-MITF. Mutations of each motif significantly reduced the transactivation, suggesting that +-MITF directly transactivated the MMCP-6 gene through these three motifs.

摘要

小鼠的mi基因座编码一种转录因子的碱性螺旋-环-螺旋-亮氨酸拉链(bHLH-Zip)蛋白家族成员(以下称为MITF)。由于小鼠肥大细胞蛋白酶6(MMCP-6)基因在mi/mi突变小鼠的肥大细胞中表达显著降低,我们研究了MITF对MMCP-6基因转录的影响。首先,我们使用逆转录病毒载体将正常(+)MITF cDNA导入mi/mi培养的肥大细胞中。+-MITF而非mi-MITF的过表达使MMCP-6基因的表达恢复正常,表明+-MITF参与了MMCP-6基因的反式激活。其次,我们通过瞬时共转染实验分析了MMCP-6基因的启动子。将受MMCP-6启动子控制的荧光素酶构建体与编码+-MITF或mi-MITF的cDNA共转染到NIH/3T3成纤维细胞中。+-MITF而非mi-MITF的共表达使荧光素酶活性增加了10倍。我们在MMCP-6启动子中发现了一个CACATG和一个CATCTG基序,这两个基序通常被bHLH-Zip型转录因子识别。我们还发现了一个被+-MITF强烈结合的GACCTG基序。这三个基序对于+-MITF对MMCP-6启动子的10倍反式激活能力是必需的。每个基序的突变都显著降低了反式激活,这表明+-MITF通过这三个基序直接反式激活了MMCP-6基因。

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