A deletion encompassing Zic3 in Bent tail, a mouse model for X-linked neural tube defects
A deletion encompassing Zic3 in Bent tail, a mouse model for X-linked neural tube defects
Bent tail is a mouse model for human neural tube defects. Bent tail mice are characterized by a shortened, kinked tail. We have observed numerous aberrations in Bent tail embryos including exencephaly, rotation defects and occasionally omphalocele, orofacial schisis and situs abnormalities. Exencephaly was seen in >10% of all embryos and resulted from a closure defect of the hindbrain. Bent tail maps to the proximal part of the X chromosome. By haplotype analysis we have appointed the Bent tail locus to a 1.1 cM interval between markers DXMit159 and DXMit143. Subsequent analysis has revealed the presence of a deletion in all affected animals. The deletion is approximately 1 Mb in size and encompasses the gene for ZIC:3, a zinc finger transcription factor expressed in murine neuroectoderm and dorsal axial mesoderm during neurulation. ZIC:3 is a homolog of the Drosophila segmentation gene odd-paired. Although the Bent tail phenotype probably is the result of the deletion of several genes, combining data on ZIC:3 expression and function of ZIC: genes in the mouse shows that deletion of Zic3 alone is compatible with a major role of this gene in the congenital malformations of the Bent tail mouse. In man, mutations in ZIC3 are associated with situs abnormalities. These patients occasionally also show spina bifida, indicating that genetic variation in human ZIC3 may contribute to other congenital malformations, including neural tube defects.
- Radboud University Nijmegen Medical Centre Netherlands
- Radboud University Nijmegen Netherlands
Homeodomain Proteins, Male, Mice, Inbred BALB C, Genetic Linkage, Identificatie van genen die betrokken zijn bij de etiologie van neurale-buisdefecten, Chromosome Mapping, Mice, Inbred Strains, DNA, Embryo, Mammalian, Mice, Inbred C57BL, Disease Models, Animal, Mice, Phenotype, Mice, Inbred DBA, Mice, Inbred CBA, Animals, Guanine Nucleotide Exchange Factors, Humans, Female, Neural Tube Defects, Identification of genetic factors involved in the etiology of neural tube defects, Gene Deletion
Homeodomain Proteins, Male, Mice, Inbred BALB C, Genetic Linkage, Identificatie van genen die betrokken zijn bij de etiologie van neurale-buisdefecten, Chromosome Mapping, Mice, Inbred Strains, DNA, Embryo, Mammalian, Mice, Inbred C57BL, Disease Models, Animal, Mice, Phenotype, Mice, Inbred DBA, Mice, Inbred CBA, Animals, Guanine Nucleotide Exchange Factors, Humans, Female, Neural Tube Defects, Identification of genetic factors involved in the etiology of neural tube defects, Gene Deletion
5 Research products, page 1 of 1
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).69 popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.Top 10% influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).Top 10% impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.Top 10%
