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一个E盒包含一个用于检测骨骼肌基因表达和甲基化区域差异的位置传感器。

An E box comprises a positional sensor for regional differences in skeletal muscle gene expression and methylation.

作者信息

Ceccarelli E, McGrew M J, Nguyen T, Grieshammer U, Horgan D, Hughes S H, Rosenthal N

机构信息

Cardiovascular Research Center, Massachusetts General Hospital-East, Charlestown, Massachusetts 02129, USA.

出版信息

Dev Biol. 1999 Sep 1;213(1):217-29. doi: 10.1006/dbio.1999.9345.

DOI:10.1006/dbio.1999.9345
PMID:10452859
Abstract

To dissect the molecular mechanisms conferring positional information in skeletal muscles, we characterized the control elements responsible for the positionally restricted expression patterns of a muscle-specific transgene reporter, driven by regulatory sequences from the MLC1/3 locus. These sequences have previously been shown to generate graded transgene expression in the segmented axial muscles and their myotomal precursors, fortuitously marking their positional address. An evolutionarily conserved E box in the MLC enhancer core, not recognized by MyoD, is a target for a nuclear protein complex, present in a variety of tissues, which includes Hox proteins and Zbu1, a DNA-binding member of the SW12/SNF2 gene family. Mutation of this E box in the MLC enhancer has only a modest positive effect on linked CAT gene expression in transfected muscle cells, but when introduced into transgenic mice the same mutation elevates CAT transgene expression in skeletal muscles, specifically releasing the rostral restriction on MLC-CAT transgene expression in the segmented axial musculature. Increased transgene activity resulting from the E box mutation in the MLC enhancer correlates with reduced DNA methylation of the distal transgenic MLC1 promoter as well as in the enhancer itself. These results identify an E box and the proteins that bind to it as a positional sensor responsible for regional differences in axial skeletal muscle gene expression and accessibility.

摘要

为了剖析赋予骨骼肌位置信息的分子机制,我们对负责肌肉特异性转基因报告基因位置受限表达模式的调控元件进行了表征,该报告基因由MLC1/3基因座的调控序列驱动。这些序列先前已被证明能在分节的轴肌及其肌节前体细胞中产生分级转基因表达,偶然地标记了它们的位置信息。MLC增强子核心中一个进化保守的E框,不被MyoD识别,是一种核蛋白复合物的靶点,该复合物存在于多种组织中,包括Hox蛋白和Zbu1,后者是SWI2/SNF2基因家族的DNA结合成员。MLC增强子中这个E框的突变对转染的肌肉细胞中连接的CAT基因表达只有适度的正向作用,但当引入转基因小鼠时,相同的突变会提高骨骼肌中CAT转基因的表达,特别是解除了分节轴肌中MLC-CAT转基因表达的头端限制。MLC增强子中E框突变导致的转基因活性增加与远端转基因MLC1启动子以及增强子本身的DNA甲基化减少相关。这些结果确定了一个E框及其结合蛋白是负责轴向骨骼肌基因表达和可及性区域差异的位置传感器。

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