Zammit Peter S, Carvajal Jaime J, Golding Jon P, Morgan Jennifer E, Summerbell Dennis, Zolnerciks Joseph, Partridge Terence A, Rigby Peter W J, Beauchamp Jonathan R
Muscle Cell Biology Group, Medical Research Council Clinical Sciences Centre, Faculty of Medicine, Imperial College, London, W12 0NN, UK.
Dev Biol. 2004 Sep 15;273(2):454-65. doi: 10.1016/j.ydbio.2004.05.038.
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.
生肌调节因子Myf5对于骨骼肌形成的起始和控制至关重要。在成年肌肉中,Myf5在卫星细胞(成熟肌肉的干细胞)中表达,但在维持肌纤维的肌核中不表达。利用Myf5(nlacZ/+)小鼠,我们现在表明Myf5也在肌梭(对拉伸敏感的机械感受器)中组成性表达,而肌肉去神经支配会诱导肌核中Myf5基因的广泛重新激活。为了确定成年肌肉中参与Myf5调控的元件,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。携带Myf5转录起始位点上游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,携带上游88 kb和59 kb的BAC虽然保留了在肌梭中的表达以及肌核中该基因座的重新激活,但无法在卫星细胞中驱动一致的表达。因此,与发育过程中一样,需要多个增强子来在成年个体中产生Myf5的完整表达模式。这些观察结果共同表明,控制成年Myf5表达的元件在遗传上是可分离的,并且可能与发育过程中控制Myf5的元件不同。这些研究是朝着鉴定参与肌肉干细胞调控的同源转录因子迈出的第一步。