Braun T, Bober E, Rudnicki M A, Jaenisch R, Arnold H H
Department of Cell and Molecular Biology, University of Braunschweig, FRG.
Development. 1994 Nov;120(11):3083-92. doi: 10.1242/dev.120.11.3083.
The expression pattern of myogenic regulatory factors and myotome-specific contractile proteins was studied during embryonic development of Myf-5 mutant mice by in situ hybridization and immunohistochemistry. In contrast to somites in wild-type embryos, no expression of myogenin and Myf-6 (MRF4), or any other myotomal markers was detected in mutant animals at E9.0 and E10.0 indicating that Myf-5 plays a crucial role during this developmental period. Significantly, the onset of MyoD expression in rostral somites of E10.5 embryos was unaffected by the Myf-5 mutation suggesting that the activation of the MyoD gene occurs independently of Myf-5 at the correct developmental time. Immediately after the activation of MyoD myogenin transcripts and protein accumulated within the myotome. The first contractile proteins of the sarcomeric apparatus appeared slightly later. By E11.5 the expression of muscle markers were indistinguishable between wild-type and Myf-5 mutant mice. The migration of muscle precursor cells that leave the somites to form limb musculature was monitored in Myf-5-mutant mice by Pax-3 expression. Pax-3-positive cells were equally found in somites and limbs of E10.0 wild-type and mutant mice indicating that myogenic factor expression at the level of somites is not a prerequisite for determination and subsequent migration of limb precursor cells.
通过原位杂交和免疫组织化学方法,研究了Myf-5突变小鼠胚胎发育过程中肌源性调节因子和体节特异性收缩蛋白的表达模式。与野生型胚胎的体节不同,在E9.0和E10.0的突变动物中未检测到生肌调节因子和Myf-6(MRF4)或任何其他体节标记物的表达,这表明Myf-5在此发育阶段起着关键作用。值得注意的是,E10.5胚胎头侧体节中MyoD表达的起始不受Myf-5突变的影响,这表明在正确的发育时间,MyoD基因的激活独立于Myf-5发生。MyoD激活后,生肌调节因子转录本和蛋白立即在体节内积累。肌节装置的首批收缩蛋白出现稍晚。到E11.5时,野生型和Myf-5突变小鼠之间肌肉标记物的表达没有区别。通过Pax-3表达监测Myf-5突变小鼠中离开体节形成肢体肌肉组织的肌肉前体细胞的迁移。在E10.0野生型和突变小鼠的体节和肢体中均同样发现了Pax-3阳性细胞,这表明体节水平的肌源性因子表达不是肢体前体细胞确定和随后迁移的先决条件。