Novel genetic tools facilitate the study of cortical neuron migration

Mamm Genome. 2016 Feb;27(1-2):8-16. doi: 10.1007/s00335-015-9615-6. Epub 2015 Dec 12.

Abstract

Key facets of mammalian forebrain cortical development include the radial migration of projection neurons and subsequent cellular differentiation into layer-specific subtypes. Inappropriate regulation of these processes can lead to a number of congenital brain defects in both mouse and human, including lissencephaly and intellectual disability. The genes regulating these processes are still not all identified, suggesting genetic analyses will continue to be a powerful tool in mechanistically studying the development of the cerebral cortex. Reelin is a molecule which we have understood to be critical for proper cortical development for many years. The precise mechanism of Reelin, however, is not fully understood. To address both of these unresolved issues, we report here the creation of a novel conditional allele of the Reelin gene and showcase the use of an Etv1-GFP transgenic line highlighting a subpopulation of the cortex: layer V pyramidal neurons. Together, these represent genetic tools which may facilitate the study of cortical development in a number of different ways.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alleles
  • Animals
  • Cell Adhesion Molecules, Neuronal / genetics
  • Cell Adhesion Molecules, Neuronal / metabolism
  • Cell Movement
  • Cerebellum / metabolism
  • Cerebellum / ultrastructure*
  • Cerebral Cortex / metabolism
  • Cerebral Cortex / ultrastructure*
  • Crosses, Genetic
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • Embryonic Stem Cells / cytology
  • Embryonic Stem Cells / metabolism
  • Extracellular Matrix Proteins / genetics
  • Extracellular Matrix Proteins / metabolism
  • Female
  • Founder Effect*
  • Gene Expression
  • Green Fluorescent Proteins / genetics
  • Green Fluorescent Proteins / metabolism
  • Hippocampus / metabolism
  • Hippocampus / ultrastructure*
  • Male
  • Mice
  • Mice, Transgenic*
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / metabolism
  • Plasmids / chemistry
  • Plasmids / metabolism
  • Pyramidal Cells / metabolism
  • Pyramidal Cells / ultrastructure*
  • Recombinant Fusion Proteins / genetics
  • Recombinant Fusion Proteins / metabolism
  • Reelin Protein
  • Serine Endopeptidases / genetics
  • Serine Endopeptidases / metabolism
  • Transcription Factors / genetics
  • Transcription Factors / metabolism
  • Transfection

Substances

  • Cell Adhesion Molecules, Neuronal
  • DNA-Binding Proteins
  • Etv1 protein, mouse
  • Extracellular Matrix Proteins
  • Nerve Tissue Proteins
  • Recombinant Fusion Proteins
  • Reelin Protein
  • Transcription Factors
  • Green Fluorescent Proteins
  • RELN protein, human
  • Reln protein, mouse
  • Serine Endopeptidases