Commissure formation in the embryonic CNS of Drosophila

Dev Biol. 1999 May 15;209(2):381-98. doi: 10.1006/dbio.1999.9235.

Abstract

In the ventral nerve cord of Drosophila most axons are organized in a simple, ladder-like pattern. Two segmental commissures connect the hemisegments along the mediolateral and two longitudinal connectives connect individual neuromeres along the anterior-posterior axis. Cells located at the midline of the developing CNS first guide commissural growth cones toward and across the midline. In later stages, midline glial cells are required to separate anterior and posterior commissures into distinct axon bundles. To unravel the genes underlying the formation of axon pattern in the embryonic ventral nerve cord, we conducted a saturating ethylmethane sulfonate mutagenesis, screening for mutations which disrupt this process. Subsequent genetic and phenotypic analyses support a sequential model of axon pattern formation in the embryonic ventral nerve cord. Specification of midline cell lineages is brought about by the action of segment polarity genes. Five genes are necessary for the establishment of the commissures. In addition to commissureless, the netrin genes, and the netrin receptor encoded by the frazzled gene, two gene functions are required for the initial formation of commissural tracts. Over 20 genes appear to be required for correct development of the midline glial cells which are necessary for the formation of distinct segmental commissures.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Axons / pathology
  • Basic Helix-Loop-Helix Transcription Factors
  • Cell Lineage
  • Central Nervous System / embryology*
  • DNA-Binding Proteins / genetics
  • DNA-Binding Proteins / metabolism
  • DNA-Binding Proteins / physiology
  • Drosophila Proteins
  • Drosophila melanogaster / embryology*
  • Drosophila melanogaster / genetics
  • Drosophila melanogaster / ultrastructure
  • Embryo, Nonmammalian / ultrastructure
  • Embryonic Development
  • Ethyl Methanesulfonate
  • Gene Expression Regulation, Developmental*
  • Genes, Insect
  • Genes, Lethal
  • Genotype
  • Insect Proteins / genetics
  • Insect Proteins / physiology
  • Morphogenesis / genetics
  • Mutagenesis
  • Nerve Growth Factors / genetics
  • Nerve Growth Factors / physiology
  • Netrin Receptors
  • Netrin-1
  • Nuclear Proteins / deficiency
  • Nuclear Proteins / genetics
  • Nuclear Proteins / metabolism
  • Nuclear Proteins / physiology
  • Phenotype
  • Receptors, Cell Surface / genetics
  • Receptors, Cell Surface / physiology
  • Tumor Suppressor Proteins

Substances

  • Basic Helix-Loop-Helix Transcription Factors
  • DNA-Binding Proteins
  • Drosophila Proteins
  • Insect Proteins
  • Nerve Growth Factors
  • Netrin Receptors
  • Nuclear Proteins
  • Receptors, Cell Surface
  • Tumor Suppressor Proteins
  • fra protein, Drosophila
  • sim protein, Drosophila
  • Netrin-1
  • Ethyl Methanesulfonate