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Myf5 expression in satellite cells and spindles in adult muscle is controlled by separate genetic elements

机译:成年肌肉中卫星细胞和纺锤体中的Myf5表达受单独的遗传元件控制

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摘要

The myogenic regulatory factor Myf5 is integral to the initiation and control of skeletal muscle formation. In adult muscle, Myf5 is expressed in satellite cells, stem cells of mature muscle, but not in the myonuclei that sustain the myofibre. Using the Myf5(nlacZ/+) mouse, we now show that Myf5 is also constitutively expressed in muscle spindles-stretch-sensitive mechanoreceptors, while muscle denervation induces extensive reactivation of the Myf5 gene in myonuclei. To identify the elements involved in the regulation of Myf5 in adult muscle, we analysed reporter gene expression in a transgenic bacterial artificial chromosome (BAC) deletion series of the Mrf4/Myf5 locus. A BAC carrying 140 kb upstream of the Myf5 transcription start site was sufficient to drive all aspects of Myf5 expression in adult muscle. In contrast, BACs carrying 88 and 59 kb upstream were unable to drive consistent expression in satellite cells, although expression in muscle spindles and reactivation of the locus in myonuclei were retained. Therefore, as during development, multiple enhancers are required to generate the full expression pattern of Myf5 in the adult. Together, these observations show that elements controlling adult Myf5 expression are genetically separable and possibly distinct from those that control Myf5 during development. These studies are a first step towards identifying cognate transcription factors involved in muscle stem cell regulation. (C) 2004 Elsevier Inc. All rights reserved
机译:肌源性调节因子Myf5是启动和控制骨骼肌形成所必需的。在成年肌肉中,Myf5在卫星细胞,成熟肌肉的干细胞中表达,但在维持肌原纤维的肌核中不表达。使用Myf5(nlacZ / +)小鼠,我们现在显示Myf5在肌纺锤体舒张敏感的机械感受器中也组成性表达,而肌肉去神经化则导致Myf5基因在肌核中广泛活化。为了确定参与成人肌Myf5调控的元素,我们分析了Mrf4 / Myf5基因座的转基因细菌人工染色体(BAC)缺失系列中的报告基因表达。在Myf5转录起始位点上游携带140 kb的BAC足以驱动成年肌肉中Myf5表达的各个方面。相比之下,携带88和59 kb上游的BAC不能驱动卫星细胞中的一致表达,尽管保留了肌肉纺锤体中的表达和肌核中基因座的重新激活。因此,如在发育期间,需要多种增强子以在成人中产生Myf5的完整表达模式。总之,这些观察结果表明,控制成年Myf5表达的元件在基因上是可分离的,并且可能与在发育过程中控制Myf5的元件不同。这些研究是鉴定参与肌肉干细胞调控的同源转录因子的第一步。 (C)2004 Elsevier Inc.保留所有权利

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