Gradients of the Drosophila Chinmo BTB-zinc finger protein govern neuronal temporal identity

被引:180
作者
Zhu, Sijun
Lin, Suewei
Kao, Chih-Fei
Awasaki, Takeshi
Chiang, Ann-Shyn
Lee, Tzumin
机构
[1] Univ Illinois, Dept Cell & Dev Biol, Urbana, IL 61801 USA
[2] Univ Illinois, Dept Mol & Integrat Physiol, Urbana, IL 61801 USA
[3] Univ Massachusetts, Dept Neurol, Sch Med, Worcester, MA 01605 USA
[4] Natl Tsing Hua Univ, Dept Life Sci, Hsinchu 30013, Taiwan
关键词
D O I
10.1016/j.cell.2006.08.045
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Many neural progenitors, including Drosophila mushroom body (MB) and projection neuron (PN) neuroblasts, sequentially give rise to different subtypes of neurons throughout development. We identified a novel BTB-zinc finger protein, named Chinmo (Chronologically inappropriate morphogenesis), that governs neuronal temporal identity during postembryonic development of the Drosophila brain. In both MB and PN lineages, loss of Chinmo autonomously causes early-born neurons to adopt the fates of late-born neurons from the same lineages. Interestingly, primarily due to a posttranscriptional control, MB neurons born at early developmental stages contain more abundant Chinmo than their later-born siblings. Further, the temporal identity of MB progeny can be transformed toward earlier or later fates by reducing or increasing Chinmo levels, respectively. Taken together, we suggest that a temporal gradient of Chinmo (Chinmo(high) -> Chinmo(low)) helps specify distinct birth order-dependent cell fates in an extended neuronal lineage.
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页码:409 / 422
页数:14
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