Franz T
Abteilung für Neuroanatomie, Universitäts-Krankenhaus Eppendorf, Hamburg, Germany.
Teratology. 1992 Dec;46(6):599-604. doi: 10.1002/tera.1420460609.
Homozygous Splotch mutant mice (Sp/Sp) die on day 14 of gestation with neural tube defects, curly tail, and malformations of neural crest derivatives. Sp1H mice, which have a radiation-induced allele of Splotch with a similar phenotype, were used for this study. The neural tube defects are always located in the lumbosacral region and in 50% of the cases also in the region of the hindbrain. In this report, rare cases of neural tube defects and tail defects among the offspring of crosses between Splotch (Sp1H) heterozygotes are presented, which are not associated with a neural crest defect. This suggests that the development of the neural tube and neural crest defects in this mutant is caused by independent mechanisms or is dependent on the dosage of the mutant gene, with different thresholds being pathogenetic in the neural tube and neural crest, respectively.
纯合子斑点突变小鼠(Sp/Sp)在妊娠第14天死亡,伴有神经管缺陷、卷尾和神经嵴衍生物畸形。Sp1H小鼠具有辐射诱导的类似表型的斑点等位基因,用于本研究。神经管缺陷总是位于腰骶部区域,50%的病例中后脑部区域也有缺陷。在本报告中,展示了斑点(Sp1H)杂合子杂交后代中罕见的神经管缺陷和尾巴缺陷病例,这些病例与神经嵴缺陷无关。这表明该突变体中神经管和神经嵴缺陷的发生是由独立机制引起的,或者取决于突变基因的剂量,神经管和神经嵴分别有不同的致病阈值。