PMID: 9651544Jul 4, 1998Paper

Role of reelin in the control of brain development

Brain Research. Brain Research Reviews
T Curran, Gabriella D'Arcangelo

Abstract

Reeler is an autosomal recessive mutation in mice that results in widespread disruption of laminated regions of the brain. We isolated a gene, reelin, that is mutated in reeler mice. The protein product of reelin has features of extracellular matrix components and it is expressed in a temporal and spatial pattern during embryonic and postnatal development consistent with the phenotypic defects in reeler mice. To understand the molecular basis of the function of Reelin, we constructed a full length reelin clone and used it to direct Reelin expression. Using this clone we found that Reelin is a secreted glycoprotein and that a highly charged C-terminal region is essential for secretion. Furthermore, we demonstrated that an amino acid sequence present in the N-terminal region of Reelin contains an epitope that is recognized by the CR-50 monoclonal antibody. CR-50 was raised against an antigen expressed in normal mouse brain that is absent in reeler mice. The interaction of CR-50 with its epitope has been shown to disrupt neuronal migration in vitro and in vivo. We used CR-50 to precipitate p385 Reelin from reticulocyte extracts programmed with reelin mRNA, from cells transfected with reelin clones and from cerebellar explants. Ree...Continue Reading

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