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Factors in the genetic background suppress the engrailed-1 cerebellar phenotype.
- Source :
-
The Journal of neuroscience : the official journal of the Society for Neuroscience [J Neurosci] 2003 Jun 15; Vol. 23 (12), pp. 5105-12. - Publication Year :
- 2003
-
Abstract
- The mouse homeodomain protein, Engrailed-1, is generally viewed as an essential player in the early establishment and maintenance of the midbrain/hindbrain region that gives rise to the cerebellum and midbrain. In keeping with this, engineered null mutations at this locus have been reported to lead to perinatal lethality accompanied by near-total absence of cerebellar and caudal midbrain structures. We report here that these cerebellar phenotypes are nearly completely suppressed on a C57BL/6J genetic background. All cell types are present and arranged properly in both the cortex and the deep nuclei, and cell counts reveal no significant absence of cerebellar Purkinje cells. Folial patterns are nearly normal, although an apparent fusion of lobules IV and V is consistently noted. Significantly, no change in the Engrailed-2 mutant phenotype occurs after a similar background switch, and whole-mount in situ hybridization reveals identical En2 expression patterns in wild-type C57BL/6J and 129/Sv mice. One likely mechanism for the En1-/- phenotype suppression is a temporal and/or spatial change in the pattern of Engrailed-2 expression apparent only in the absence of Engrailed-1. In support of this, C57BL/6-En1-/- embryos that are also En2+/- lack a cerebellum and caudal midbrain: a phenotype identical to 129/Sv-En1-/- mice.
- Subjects :
- Abnormalities, Multiple genetics
Abnormalities, Multiple pathology
Alleles
Animals
Cell Count
Cerebellum metabolism
Cerebellum pathology
Fetal Viability genetics
Gene Expression Regulation, Developmental
Gene Transfer Techniques
Heterozygote
Homeodomain Proteins biosynthesis
Limb Deformities, Congenital genetics
Mice
Mice, Inbred C57BL
Mice, Inbred Strains
Mice, Neurologic Mutants
Mutation
Nervous System Malformations pathology
Penetrance
Phenotype
Purkinje Cells pathology
Sternum abnormalities
Cerebellum abnormalities
Homeodomain Proteins genetics
Nervous System Malformations genetics
Suppression, Genetic
Subjects
Details
- Language :
- English
- ISSN :
- 1529-2401
- Volume :
- 23
- Issue :
- 12
- Database :
- MEDLINE
- Journal :
- The Journal of neuroscience : the official journal of the Society for Neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 12832534