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CCAAT 位移蛋白与成对组蛋白基因转录所需的共享调控元件之间的相互作用。

Interaction of the CCAAT displacement protein with shared regulatory elements required for transcription of paired histone genes.

作者信息

el-Hodiri H M, Perry M

机构信息

Department of Biochemistry and Molecular Biology, University of Texas M. D. Anderson Cancer Center, Houston 77030, USA.

出版信息

Mol Cell Biol. 1995 Jul;15(7):3587-96. doi: 10.1128/MCB.15.7.3587.

Abstract

The H2A and H2B genes of the Xenopus xlh3 histone gene cluster are transcribed in opposite directions from initiation points located approximately 235 bp apart. The close proximity of these genes to one another suggests that their expression may be controlled by either a single bidirectional promoter or by separate promoters. Our analysis of the transcription of histone gene pairs containing deletions and site-specific mutations of intergenic DNA revealed that both promoters are distinct but that they overlap physically and share multiple regulatory elements, providing a possible basis for the coordinate regulation of their in vivo activities. Using the intergenic DNA fragment as a probe and extracts from mammalian and amphibian cells, we observed the formation of a specific complex containing the CCAAT displacement protein (CDP). The formation of the CDP-containing complex was not strictly dependent on any single element in the intergenic region but instead required the presence of at least two of the three CCAAT motifs. Interestingly, similar CDP-containing complexes were formed on the promoters from the three other histone genes. The binding of CDP to histone gene promoters may contribute to the coordination of their activities during the cell cycle and early development.

摘要

非洲爪蟾xlh3组蛋白基因簇的H2A和H2B基因从相距约235 bp的起始点以相反方向转录。这些基因彼此紧密相邻,这表明它们的表达可能由单个双向启动子或由单独的启动子控制。我们对含有基因间DNA缺失和位点特异性突变的组蛋白基因对转录的分析表明,两个启动子是不同的,但它们在物理上重叠并共享多个调控元件,为它们体内活性的协调调控提供了可能的基础。使用基因间DNA片段作为探针以及来自哺乳动物和两栖动物细胞的提取物,我们观察到形成了一种含有CCAAT置换蛋白(CDP)的特异性复合物。含CDP复合物的形成并不严格依赖于基因间区域中的任何单个元件,而是需要三个CCAAT基序中至少两个的存在。有趣的是,在其他三个组蛋白基因的启动子上也形成了类似的含CDP复合物。CDP与组蛋白基因启动子的结合可能有助于在细胞周期和早期发育过程中协调它们的活性。

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