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First published online 11 January 2006
doi: 10.1242/dev.02236
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1 Interdepartmental Program in Neuroscience, University of Utah, Salt Lake City,
Utah 84112, USA.
2 Department of Human Genetics, University of Utah, Salt Lake City, Utah 84112,
USA.
Author for correspondence (e-mail:
mario.capecchi{at}genetics.utah.edu)
Accepted 5 December 2005
Olig gene expression is proposed to mark the common progenitors of motoneurons and oligodendrocytes. In an attempt to further dissect the in vivo lineage relationships between motoneurons and oligodendrocytes, we used a conditional cell-ablation approach to kill Olig-expressing cells. Although differentiated motoneurons and oligodendrocytes were eliminated, our ablation study revealed a continuous generation and subsequent death of their precursors. Most remarkably, a normal number of oligodendrocyte precursors are formed at day 12 of mouse development, after all motoneuron precursors have been killed. The data presented herein supports a sequential model in which motoneuron and oligodendrocyte precursors are sequentially generated in vivo from neuroepithelial stem cells, but do not share a common lineage-restricted progenitor.
Key words: Motoneurons, Oligodendrocytes, Glia, Diphtheria toxin, Cell ablation
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