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PEBP2/CBF 与微小转录因子(MITF)协同激活小鼠肥大细胞蛋白酶 6 基因的转录。

Synergy of PEBP2/CBF with mi transcription factor (MITF) for transactivation of mouse mast cell protease 6 gene.

作者信息

Ogihara H, Kanno T, Morii E, Kim D K, Lee Y M, Sato M, Kim W Y, Nomura S, Ito Y, Kitamura Y

机构信息

Department of Pathology, Osaka University Medical School, 2-2 Yamada-oka, Suita, Osaka 565-0871, Japan.

出版信息

Oncogene. 1999 Aug 12;18(32):4632-9. doi: 10.1038/sj.onc.1202844.

DOI:10.1038/sj.onc.1202844
PMID:10467408
Abstract

The mi locus encodes a member of the basic - helix - loop - helix - leucine zipper (bHLH-Zip) protein family of transcription factors (hereafter called MITF). Although the bHLH-Zip family transcription factors generally recognize and bind CANNTG motifs, the expression of mouse mast cell protease 6 (MMCP-6) gene is regulated by MITF through the GACCTG motif in the promoter region. The GACCTG motif was partly overlapped the TGTGGTC sequence, which was bound by polyomavirus enhancer binding protein 2 (PEBP2). In the present study, the effect of PEBP2 on the expression of MMCP-6 gene was examined. PEBP2 that is composed of alpha and beta subunits was expressed by mast cell lines and cultured mast cells derived from spleen. The overexpression of dominant negative PEBP2 cDNA reduced the expression of MMCP-6. Moreover, the simultaneous transfection of the plasmid containing MITF cDNA and the plasmid containing PEBP2 cDNA increased the MMCP-6 promoter activity. For the synergistic action of PEBP2 and MITF, the intact GACCTG and TGTGGTC motifs were prerequisite. The PEBP2alphaB1 mutant which lacked the region downstream from the Runt domain did not bind MITF and lost the synergistic function. These results indicated that PEBP2 and MITF synergistically transactivated the MMCP-6 gene and that the region downstream from the Runt domain of PEBP2alphaB1 was essential for the physical and functional interactions with MITF.

摘要

mi基因座编码一种转录因子,属于碱性-螺旋-环-螺旋-亮氨酸拉链(bHLH-Zip)蛋白家族成员(以下称为MITF)。尽管bHLH-Zip家族转录因子通常识别并结合CANNTG基序,但小鼠肥大细胞蛋白酶6(MMCP-6)基因的表达受MITF通过启动子区域中的GACCTG基序调控。GACCTG基序部分与多瘤病毒增强子结合蛋白2(PEBP2)结合的TGTGGTC序列重叠。在本研究中,检测了PEBP2对MMCP-6基因表达的影响。由α和β亚基组成的PEBP2由肥大细胞系和源自脾脏的培养肥大细胞表达。显性负性PEBP2 cDNA的过表达降低了MMCP-6的表达。此外,同时转染含有MITF cDNA的质粒和含有PEBP2 cDNA的质粒可增加MMCP-6启动子活性。对于PEBP2和MITF的协同作用,完整的GACCTG和TGTGGTC基序是必不可少的。缺乏Runt结构域下游区域的PEBP2αB1突变体不与MITF结合并失去协同功能。这些结果表明,PEBP2和MITF协同反式激活MMCP-6基因,并且PEBP2αB1的Runt结构域下游区域对于与MITF的物理和功能相互作用至关重要。

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Oncogene. 1999 Aug 12;18(32):4632-9. doi: 10.1038/sj.onc.1202844.
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