Repulsive guidance molecule (RGM) gene function is required for neural tube closure but not retinal topography in the mouse visual system

J Neurosci. 2004 Jan 28;24(4):808-18. doi: 10.1523/JNEUROSCI.4610-03.2004.

Abstract

The establishment of topographic projections in the developing visual system depends on the spatially and temporally controlled expression of axon guidance molecules. In the developing chick tectum, the graded expression of the repulsive guidance molecule (RGM) has been proposed to be involved in controlling the topography of the retinal ganglion cell (RGC) axon termination zones along the anteroposterior axis of the tectum. We now show that there are three mouse proteins homologous to chick RGM displaying similar proteolytic processing but exhibiting differential cell-surface targeting by glycosyl phosphatidylinositol anchor addition. Two members of this gene family (mRGMa and mRGMb) are expressed in complementary patterns in the nervous system, and mRGMa is expressed prominently in the superior colliculus at the time of anteroposterior targeting of RGC axons. The third member of the family (mRGMc) is expressed almost exclusively in skeletal muscles. Functional studies in the mouse reveal a role for mRGMa in controlling cephalic neural tube closure, thus defining an unexpected role for mRGMa in early embryonic development. In contrast, mRGMa mutant mice did not exhibit defects in anteroposterior targeting of RGC axons to their stereotypic termination zones in the superior colliculus.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Animals, Newborn
  • Axons / metabolism
  • Axons / physiology
  • Bromodeoxyuridine
  • COS Cells
  • Cell Adhesion Molecules, Neuronal
  • Central Nervous System / embryology
  • Central Nervous System / metabolism*
  • Chick Embryo
  • Cloning, Molecular
  • Ephrin-A5 / genetics
  • GPI-Linked Proteins
  • Gene Expression Regulation, Developmental*
  • Glycosylphosphatidylinositols / metabolism
  • In Situ Hybridization
  • Membrane Proteins / genetics
  • Membrane Proteins / physiology*
  • Mice
  • Mice, Mutant Strains
  • Molecular Sequence Data
  • Multigene Family / genetics
  • Muscle Proteins / biosynthesis
  • Muscle Proteins / genetics
  • Muscle, Skeletal / metabolism
  • Nerve Tissue Proteins / biosynthesis
  • Nerve Tissue Proteins / genetics
  • Nerve Tissue Proteins / physiology*
  • Organ Specificity
  • Retina / embryology
  • Retina / metabolism*
  • Sequence Homology, Amino Acid
  • Superior Colliculi / embryology
  • Superior Colliculi / metabolism

Substances

  • Cell Adhesion Molecules, Neuronal
  • Ephrin-A5
  • GPI-Linked Proteins
  • Glycosylphosphatidylinositols
  • Membrane Proteins
  • Muscle Proteins
  • Nerve Tissue Proteins
  • Rgma protein, mouse
  • Rgmb protein, mouse
  • Rgmc protein, mouse
  • Bromodeoxyuridine