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Common core sequences are found in skeletal muscle slow- and fast-fiber-type-specific regulatory elements.

机译:在骨骼肌慢纤维和快纤维类型特异性调节元件中发现共同的核心序列。

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摘要

The molecular mechanisms generating muscle diversity during development are unknown. The phenotypic properties of slow- and fast-twitch myofibers are determined by the selective transcription of genes coding for contractile proteins and metabolic enzymes in these muscles, properties that fail to develop in cultured muscle. Using transgenic mice, we have identified regulatory elements in the evolutionarily related troponin slow (TnIs) and fast (TnIf) genes that confer specific transcription in either slow or fast muscles. Analysis of serial deletions of the rat TnIs upstream region revealed that sequences between kb -0.95 and -0.5 are necessary to confer slow-fiber-specific transcription; the -0.5-kb fragment containing the basal promoter was inactive in five transgenic mouse lines tested. We identified a 128-bp regulatory element residing at kb -0.8 that, when linked to the -0.5-kb TnIs promoter, specifically confers transcription to slow-twitch muscles. To identify sequences directing fast-fiber-specific transcription, we generated transgenic mice harboring a construct containing the TnIs kb -0.5 promoter fused to a 144-bp enhancer derived from the quail TnIf gene. Mice harboring the TnIf/TnIs chimera construct expressed the transgene in fast but not in slow muscles, indicating that these regulatory elements are sufficient to confer fiber-type-specific transcription. Alignment of rat TnIs and quail TnIf regulatory sequences indicates that there is a conserved spatial organization of core elements, namely, an E box, a CCAC box, a MEF-2-like sequence, and a previously uncharacterized motif. The core elements were shown to bind their cognate factors by electrophoretic mobility shift assays, and their mutation demonstrated that the TnIs CCAC and E boxes are necessary for transgene expression. Our results suggest that the interaction of closely related transcriptional protein-DNA complexes is utilized to specify fiber type diversity.
机译:在发育过程中产生肌肉多样性的分子机制尚不清楚。慢肌和快肌肌纤维的表型特性是由编码这些肌肉中收缩蛋白和代谢酶的基因的选择性转录所决定的,这些特性在培养的肌肉中无法发挥。使用转基因小鼠,我们已经确定了与进化相关的肌钙蛋白慢(TnIs)和快(TnIf)基因在慢或快肌肉中赋予特定转录的调控元件。对大鼠TnIs上游区域的系列缺失进行分析后发现,kb -0.95和-0.5之间的序列对于赋予慢纤维特异性转录是必需的。含有基础启动子的-0.5-kb片段在测试的5个转基因小鼠品系中没有活性。我们鉴定了一个位于kb -0.8处的128 bp调控元件,当与-0.5 kb TnIs启动子连接时,可将转录特异赋予慢肌。为了鉴定指导快速纤维特异性转录的序列,我们生成了转基因小鼠,该小鼠带有一个构建体,该构建体包含与衍生自鹌鹑TnIf基因的144-bp增强子融合的TnIs kb -0.5启动子。携带TnIf / TnIs嵌合体构建体的小鼠在快速肌肉中表达转基因,但在慢速肌肉中不表达转基因,表明这些调节元件足以赋予纤维类型特异性转录。大鼠TnIs和鹌鹑TnIf调控序列的比对表明存在核心元素的保守空间组织,即E框,CCAC框,MEF-2样序列和以前未知的基序。通过电泳迁移率变动分析显示核心元件结合其同源因子,并且它们的突变表明TnIs CCAC和E盒对于转基因表达是必需的。我们的结果表明,密切相关的转录蛋白-DNA复合物的相互作用可用于指定纤维类型的多样性。

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