Assembly of the brainstem cochlear nuclear complex is revealed by intersectional and subtractive genetic fate maps

Neuron. 2006 Apr 20;50(2):205-18. doi: 10.1016/j.neuron.2006.03.014.


The cochlear nuclear complex (CN) is the entry point for central auditory processing. Although constituent neurons have been studied physiologically, their embryological origins and molecular profiles remain obscure. Applying intersectional and subtractive genetic fate mapping approaches, we show that this complex develops modularly from genetically separable progenitor populations arrayed as rostrocaudal microdomains within and outside the hindbrain (lower) rhombic lip (LRL). The dorsal CN subdivision, structurally and topographically similar to the cerebellum, arises from microdomains unexpectedly caudal and noncontiguous to cerebellar primordium; ventral CN subdivisions arise from more rostral LRL. Magnocellular regions receive contributions from LRL and coaxial non-lip progenitors; contrastingly, ensheathing granule cells derive principally from LRL. Also LRL-derived and molecularly similar to CN granule cells are precerebellar mossy fiber neurons; surprisingly, these ostensibly intertwined populations have separable origins and adjacent but segregated migratory streams. Together, these findings provide new platforms for investigating the development and evolution of auditory and cerebellar systems.

Publication types

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

MeSH terms

  • Animals
  • Auditory Pathways / cytology
  • Auditory Pathways / embryology*
  • Cell Movement / physiology
  • Cochlear Nucleus / embryology*
  • DNA Nucleotidyltransferases / genetics
  • Gene Expression Profiling
  • Gene Expression Regulation, Developmental
  • Immunohistochemistry
  • In Situ Hybridization
  • Integrases / genetics
  • Mice
  • Mice, Transgenic
  • Neurons / cytology
  • Neurons / physiology*
  • RNA, Messenger / analysis
  • Stem Cells / cytology
  • Stem Cells / physiology*
  • Transgenes


  • RNA, Messenger
  • Cre recombinase
  • DNA Nucleotidyltransferases
  • FLP recombinase
  • Integrases