Heterozygous Dab1 null mutation disrupts neocortical and hippocampal development.

Abstract

Loss-of-function mutations in Reelin and DAB1 signaling pathways disrupt proper neuronal positioning in the cerebral neocortex and hippocampus, but the underlying molecular mechanisms remain elusive. Here we report that heterozygous yotari mice harboring a single autosomal recessive yotari mutation of Dab1 exhibited a thinner neocortical layer 1 than wild-type mice on postnatal day 7. However, a birth-dating study suggested that this reduction was not caused by failure of neuronal migration. In utero electroporation-mediated sparse labeling revealed that the superficial layer neurons of heterozygous yotari mice tended to elongate their apical dendrites within layer 2 than within layer 1. In addition, the CA1 pyramidal cell layer in the caudo-dorsal hippocampus was abnormally split in heterozygous yotari mice, and a birth-dating study revealed that this splitting was caused mainly by migration failure of late-born pyramidal neurons. Adeno-associated virus-mediated sparse labeling further showed that many pyramidal cells within the split cell had misoriented apical dendrites. These results suggest that regulation of neuronal migration and positioning by Reelin-DAB1 signaling pathways has unique dependencies on Dab1 gene dosage in different brain regions.Significance StatementDAB1 is a cytoplasmic adaptor protein essential for transmission of the extracellular Reelin signal to cytoplasmic proteins that regulate cortical development. In this study, we found that Dab1 is haplosufficient for the regulation of neuronal migration but haploinsufficient for control of layer 1 thickness in the cerebral neocortex. Alternatively, the migration of a subpopulation of hippocampal pyramidal neurons is sensitive to Dab1 gene haploinsufficiency. This study suggests that neural development in the cerebral neocortex and hippocampus are differentially sensitive to Dab1 gene dose.