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The bHLH transcription factor Olig3 marks the dorsal neuroepithelium of the hindbrain and is essential for the development of brainstem nuclei

Item Type:Article
Title:The bHLH transcription factor Olig3 marks the dorsal neuroepithelium of the hindbrain and is essential for the development of brainstem nuclei
Creators Name:Storm, R. and Cholewa-Waclaw, J. and Reuter, K. and Broehl, D. and Sieber, M. and Treier, M. and Mueller, T. and Birchmeier, C.
Abstract:The Olig3 gene encodes a bHLH factor that is expressed in the ventricular zone of the dorsal alar plate of the hindbrain. We found that the Olig3(+) progenitor domain encompassed subdomains that co-expressed Math1, Ngn1, Mash1 and Ptf1a. Olig3(+) cells give rise to neuronal types in the dorsal alar plate that we denote as class A neurons. We used genetic lineage tracing to demonstrate that class A neurons contribute to the nucleus of the solitary tract and to precerebellar nuclei. The fate of class A neurons was not correctly determined in Olig3 mutant mice. As a consequence, the nucleus of the solitary tract did not form, and precerebellar nuclei, such as the inferior olivary nucleus, were absent or small. At the expense of class A neurons, ectopic Lbx1(+) neurons appeared in the alar plate in Olig3 mutant mice. By contrast, electroporation of an Olig3 expression vector in the chick hindbrain suppressed the emergence of Lbx1(+) neurons. Climbing fiber neurons of the inferior olivary nucleus express Foxd3 and require Olig3 as well as Ptf1a for the determination of their fate. We observed that electroporation of Olig3 and Ptf1a expression vectors, but not either alone, induced Foxd3. We therefore propose that Olig3 can cooperate with Ptf1a to determine the fate of climbing fiber neurons of the inferior olivary nucleus.
Keywords:Fate Mapping, Neuronal Fate, Basic Helix-Loop-Helix Transcription Factor, Brain Stem, Electroporation, Neuroepithelial Cells, Neurogenesis, Pregnancy, Rhombencephalon, Spinal Cord, Animals, Mice, Chick Embryo
Source:Development
ISSN:0950-1991
Publisher:Company of Biologists (U.K.)
Volume:136
Number:2
Page Range:295-305
Date:January 2009
Official Publication:https://doi.org/10.1242/dev.027193
PubMed:View item in PubMed

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