Drosophila homeodornain protein Nkx6 coordinates motoneuron subtype identity and axonogenesis

被引:50
作者
Broihier, HT
Kuzin, A
Zhu, Y
Odenwald, W
Skeath, JB
机构
[1] Washington Univ, Sch Med, Dept Genet, St Louis, MO 63110 USA
[2] NINDS, Neural Cell Fate Determinants Sect, NIH, Bethesda, MD 20892 USA
来源
DEVELOPMENT | 2004年 / 131卷 / 21期
关键词
Drosophila melanogaster; neuronal fate specification; motoneurons; interneurons; axon outgrowth; Nkx6; hb9 (exex); lim3; islet; eve; vnd;
D O I
10.1242/dev.01394
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The regulatory networks acting in. individual neurons to control their stereotyped differentiation, connectivity, and function are not well understood. Here, we demonstrate that homeodomain protein Nkx6 is a key member of the genetic network of transcription factors that specifies neuronal fates in Drosophila. Nkx6 collaborates with the homeodomain protein Hb9 to specify ventrally projecting motoneuron fate and to repress dorsally projecting motoneuron fate. While Nkr6 acts in parallel with hb9 to regulate motoneuron fate, we find that Nkr6 plays a distinct role to promote axonogenesis, as axon growth of Nkx6- positive motoneurons is severely compromised in Nkx6 mutant embryos. Furthermore, Nkx6 is necessary for the expression of the neural adhesion molecule Fasciclin III in Nkx6-positive motoneurons. Thus, this work demonstrates that Nkx6 acts in a specific neuronal population to link neuronal subtype identity to neuronal morphology and connectivity.
引用
收藏
页码:5233 / 5242
页数:10
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