Franz T, Kothary R, Surani M A, Halata Z, Grim M
Anatomisches Institut, Abteilung für Neuroanatomie, Universitäts-Krankenhaus Eppendorf, Hamburg, Germany.
Anat Embryol (Berl). 1993 Feb;187(2):153-60. doi: 10.1007/BF00171747.
Homozygosity for the Splotch mutation causes neural tube and neural crest defects in mice. It has been demonstrated that Splotch mutant mice carry mutations in the homeodomain of the Pax-3 gene. Pax-3 is expressed in the neural tube, some neural crest derivatives, the mesenchyme of the limb bud and the somites. We have examined the development of the somite-derived skeletal muscles in homozygotes carrying the Splotch (Sp1H) mutation. Our results suggest that the Splotch mutation affects the development of skeletal muscles in a region-specific way: 1. The expression of the CMZ transgene in homozygotes reveals a disorganisation of the dermomyotome in whole stained embryos. 2. The axial musculature is reduced in size along a rostro-caudal gradient. 3. The muscle anlagen in the limbs develop much more slowly. Muscles of the head and the ventral body wall are normally developed in the mutant on day 13.5 of gestation. Recently, it has been shown that the myogenic precursors of the limbs are derived from the lateral half of the somite. The specific disturbance of muscle development in the limbs of Splotch mutants thus suggests a role for Pax-3 in the organisation of the somite, the production of trophic factors in the limb mesenchyme or an alteration of myogenic and mesenchymal cells.
斑点突变的纯合性会导致小鼠出现神经管和神经嵴缺陷。已证明斑点突变小鼠在Pax - 3基因的同源结构域中携带突变。Pax - 3在神经管、一些神经嵴衍生物、肢芽间充质和体节中表达。我们研究了携带斑点(Sp1H)突变的纯合子中体节衍生骨骼肌的发育情况。我们的结果表明,斑点突变以区域特异性方式影响骨骼肌的发育:1. 纯合子中CMZ转基因的表达显示整个染色胚胎中皮肌节出现紊乱。2. 轴向肌肉组织沿头 - 尾梯度尺寸减小。3. 肢体内的肌肉原基发育要慢得多。在妊娠第13.5天,突变体头部和腹侧体壁的肌肉发育正常。最近,研究表明肢体的生肌前体源自体节的外侧半部分。因此,斑点突变体肢体中肌肉发育的特定紊乱表明Pax - 3在体节组织形成、肢体间充质中营养因子的产生或生肌细胞和间充质细胞的改变中发挥作用。