Lhx2 selector activity specifies cortical identity and suppresses hippocampal organizer fate

Science. 2008 Jan 18;319(5861):304-9. doi: 10.1126/science.1151695.

Abstract

The earliest step in creating the cerebral cortex is the specification of neuroepithelium to a cortical fate. Using mouse genetic mosaics and timed inactivations, we demonstrated that Lhx2 acts as a classic selector gene and essential intrinsic determinant of cortical identity. Lhx2 selector activity is restricted to an early critical period when stem cells comprise the cortical neuroepithelium, where it acts cell-autonomously to specify cortical identity and suppress alternative fates in a spatially dependent manner. Laterally, Lhx2 null cells adopt antihem identity, whereas medially they become cortical hem cells, which can induce and organize ectopic hippocampal fields. In addition to providing functional evidence for Lhx2 selector activity, these findings show that the cortical hem is a hippocampal organizer.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Cell Aggregation
  • Cerebral Cortex / cytology
  • Cerebral Cortex / embryology*
  • Cerebral Cortex / metabolism
  • Chimera
  • Dentate Gyrus / cytology
  • Dentate Gyrus / embryology
  • Dentate Gyrus / metabolism
  • Embryonic Induction
  • Embryonic Stem Cells / metabolism
  • Epithelium / embryology
  • Epithelium / metabolism
  • Gene Expression Regulation, Developmental
  • Hippocampus / cytology
  • Hippocampus / embryology*
  • Homeodomain Proteins / genetics*
  • Homeodomain Proteins / metabolism*
  • LIM-Homeodomain Proteins
  • Mice
  • Mice, Knockout
  • Mutation
  • Neuroepithelial Cells / cytology
  • Neuroepithelial Cells / metabolism
  • Organizers, Embryonic / embryology
  • Organizers, Embryonic / physiology*
  • Prosencephalon / embryology
  • Prosencephalon / metabolism
  • Pyramidal Cells / cytology
  • Pyramidal Cells / embryology
  • Recombination, Genetic
  • Telencephalon / cytology
  • Telencephalon / embryology
  • Transcription Factors / genetics*
  • Transcription Factors / metabolism*

Substances

  • Homeodomain Proteins
  • LIM-Homeodomain Proteins
  • Lhx2 protein, mouse
  • Transcription Factors