Control of roof plate formation by Lmx1a in the developing spinal cord

Development. 2004 Jun;131(11):2693-705. doi: 10.1242/dev.01139.

Abstract

Numerous studies have identified the roof plate as an embryonic signaling center critical for dorsal central nervous system patterning, but little is known about mechanisms that control its formation and its separation from clonally related neural crest cells and dI1 sensory interneurons. We demonstrate that the LIM homeodomain transcription factor, Lmx1a, mutated in the dreher mouse, acts to withdraw dorsal spinal cord progenitors from the cell cycle and simultaneously direct their differentiation into functional roof plate cells. Lmx1a cell-autonomously represses the dI1 progenitor fate, distinguishing the roof plate and dI1 interneuron programs, two major developmental programs of the dorsal neural tube. Lmx1a is not directly involved in neural crest development. We establish that Bmp signaling from epidermal ectoderm is necessary and sufficient for inducing Lmx1a and other co-factors that also regulate the extent of roof plate induction. We conclude that Lmx1a controls multiple aspects of dorsal midline patterning and is a major mediator of early Bmp signaling in the developing spinal cord.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Avian Proteins*
  • Body Patterning
  • Bone Morphogenetic Protein 4
  • Bone Morphogenetic Proteins / metabolism
  • Cell Cycle / genetics
  • Cell Differentiation
  • Chick Embryo
  • DNA-Binding Proteins*
  • Embryonic Induction
  • Gene Expression Regulation, Developmental*
  • Homeodomain Proteins / genetics*
  • Homeodomain Proteins / metabolism
  • LIM-Homeodomain Proteins
  • MafB Transcription Factor
  • Mice
  • Mice, Mutant Strains
  • Neural Crest / cytology
  • Neurons / cytology
  • Oncogene Proteins / genetics
  • Oncogene Proteins / metabolism
  • Proto-Oncogene Proteins / metabolism
  • Signal Transduction
  • Spinal Cord / cytology*
  • Spinal Cord / embryology*
  • Stem Cells / physiology
  • Trans-Activators / genetics
  • Trans-Activators / metabolism
  • Transcription Factors*
  • Wnt Proteins

Substances

  • Avian Proteins
  • Bmp4 protein, mouse
  • Bone Morphogenetic Protein 4
  • Bone Morphogenetic Proteins
  • DNA-Binding Proteins
  • Homeodomain Proteins
  • LIM-Homeodomain Proteins
  • Lmx1a protein, mouse
  • MafB Transcription Factor
  • Mafb protein, mouse
  • Oncogene Proteins
  • Proto-Oncogene Proteins
  • Trans-Activators
  • Transcription Factors
  • Wnt Proteins
  • maf-B protein, chicken