Kucharczuk K L, Love C M, Dougherty N M, Goldhamer D J
Department of Cell and Developmental Biology, University of Pennsylvania School of Medicine, 36th and Hamilton Walk, Philadelphia, PA 19104, USA.
Development. 1999 May;126(9):1957-65. doi: 10.1242/dev.126.9.1957.
Skeletal muscle lineage determination is regulated by the myogenic regulatory genes, MyoD and Myf-5. Previously, we identified a 258 bp core enhancer element 20 kb 5' of the MyoD gene that regulates MyoD gene activation in mouse embryos. To elucidate the cis control mechanisms that regulate MyoD transcription, we have mutagenized the entire core enhancer using linker-scanner mutagenesis, and have tested the transcriptional activity of enhancer mutants using lacZ reporter gene expression in transgenic mouse embryos. In total, 83 stable transgenic lines representing 17 linker-scanner mutations were analyzed in midgestational mouse embryos. Eight linker-scanner mutations resulted in a partial or complete loss of enhancer activity, demonstrating that MyoD is primarily under positive transcriptional control. Six of these mutations reduced or abolished transgene expression in all skeletal muscle lineages, indicating that activation of MyoD expression in trunk, limb and head musculature is regulated, in part, by shared transcriptional mechanisms. Interestingly, however, two adjacent linker-scanner mutations (LS-14 and LS-15) resulted in a dramatic reduction in transgene expression specifically in myotomes at 11.5 days. At later stages, transgene expression was absent or greatly reduced in myotomally derived muscles including epaxial muscles (deep back muscles) and hypaxial muscles of the body wall (intercostal muscles, abdominal wall musculature). In contrast, head muscles, as well as muscles of the body derived from migrating muscle progenitor cells (e.g. limb, diaphragm), were unaffected by these mutations. In Pax-3-mutant mice, LS-14 and LS-15 transgene expression was eliminated in the body, but was unaffected in the head, yielding an identical expression pattern to the endogenous MyoD gene in mice mutant for both Myf-5 and Pax-3. These data support the hypothesis that LS-14 and LS-15 define the core enhancer targets for Myf-5-dependent activation of MyoD in myotomal muscles.
骨骼肌谱系的确定受成肌调节基因MyoD和Myf-5调控。此前,我们在MyoD基因5'端20 kb处鉴定出一个258 bp的核心增强子元件,其可在小鼠胚胎中调节MyoD基因的激活。为阐明调控MyoD转录的顺式控制机制,我们利用接头扫描诱变对整个核心增强子进行了诱变,并在转基因小鼠胚胎中使用lacZ报告基因表达测试了增强子突变体的转录活性。总共在妊娠中期的小鼠胚胎中分析了代表17个接头扫描突变的83个稳定转基因系。八个接头扫描突变导致增强子活性部分或完全丧失,表明MyoD主要受正转录调控。其中六个突变降低或消除了所有骨骼肌谱系中的转基因表达,表明躯干、肢体和头部肌肉组织中MyoD表达的激活部分受共享转录机制调控。然而,有趣的是,两个相邻的接头扫描突变(LS-14和LS-15)导致转基因表达在11.5天时在体节中显著降低。在后期阶段,包括轴上肌(背部深层肌肉)和体壁的轴下肌(肋间肌、腹壁肌肉组织)在内的源自体节的肌肉中,转基因表达缺失或大幅降低。相比之下,头部肌肉以及源自迁移性肌肉祖细胞的身体肌肉(如肢体、膈肌)不受这些突变影响。在Pax-3突变小鼠中,LS-14和LS-15转基因表达在身体中被消除,但在头部不受影响,产生了与Myf-5和Pax-3双突变小鼠中内源性MyoD基因相同的表达模式。这些数据支持以下假设:LS-14和LS-15定义了Myf-5依赖性激活体节肌肉中MyoD的核心增强子靶点。