P63 is an essential proapoptotic protein during neural development

被引:102
作者
Jacobs, WB
Govoni, G
Ho, D
Atwal, JK
Barnabe-Heider, F
Keyes, WM
Mills, AA
Miller, FD
Kaplan, DR [1 ]
机构
[1] Univ Toronto, Hosp Sick Children, Canc Res Program, Toronto, ON M5G 1X8, Canada
[2] Univ Toronto, Hosp Sick Children, Dev Biol Program, Toronto, ON M5G 1X8, Canada
[3] Univ Toronto, Inst Med Sci, Toronto, ON M5G 1X8, Canada
[4] Univ Toronto, Div Neurosurg, Toronto, ON M5G 1X8, Canada
[5] Univ Toronto, Dept Mol & Med Genet, Toronto, ON M5G 1X8, Canada
[6] Univ Toronto, Dept Physiol, Toronto, ON M5G 1X8, Canada
[7] McGill Univ, Dept Neurol & Neurosurg, Montreal, PQ H3A 2B4, Canada
[8] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
基金
加拿大自然科学与工程研究理事会; 加拿大健康研究院;
关键词
D O I
10.1016/j.neuron.2005.10.027
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The p53 family member p63 is required for nonneural development, but has no known role in the nervous system. Here, we define an essential proapoptotic role for p63 during naturally occurring neuronal death. Sympathetic neurons express full-length TAp63 during the developmental death period, and TAp63 levels increase following NGF withdrawal. Overexpression of TAp63 causes neuronal apoptosis in the presence of NGF, while cultured p63(-/-) neurons are resistant to apoptosis following NGF withdrawal. TAp63 is also essential in vivo, since embryonic p63(-/-) mice display a deficit in naturally occurring sympathetic neuron death. While both TAp63 and p53 induce similar apoptotic signaling proteins and require BAX expression and function for their effects, TAp63 induces neuronal death in the absence of p53, but p53 requires coincident p63 expression for its proapoptotic actions. Thus, p63 is essential for developmental neuronal death, likely functioning both on its own, and as an obligate proapoptotic partner for p53.
引用
收藏
页码:743 / 756
页数:14
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