Alternative Functions of Core Cell Cycle Regulators in Neuronal Migration, Neuronal Maturation, and Synaptic Plasticity

被引:92
作者
Frank, Christopher L. [1 ,2 ]
Tsai, Li-Huei [1 ,2 ,3 ]
机构
[1] MIT, Picower Inst Learning & Memory, Dept Brain & Cognit Sci, Cambridge, MA 02139 USA
[2] Howard Hughes Med Inst, Cambridge, MA 02139 USA
[3] Harvard & Massachusetts Inst Technol, Broad Inst, Stanley Ctr Psychiat Res, Cambridge, MA 02139 USA
关键词
ANAPHASE-PROMOTING COMPLEX; ORIGIN RECOGNITION COMPLEX; POLO-LIKE KINASE; SISTER-CHROMATID COHESION; DE-LANGE-SYNDROME; SCF-BETA-TRCP; CAMKII MESSENGER-RNA; UBIQUITIN LIGASE; DNA-REPLICATION; AURORA-A;
D O I
10.1016/j.neuron.2009.03.029
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Recent studies have demonstrated that boundaries separating a cycling cell from a postmitotic neuron are not as concrete as expected. Novel and unique physiological functions in neurons have been ascribed for proteins fundamentally required for cell cycle progression and control. These "core" cell cycle regulators serve diverse postmitotic functions that span various developmental stages of a neuron, including neuronal migration, axonal elongation, axon pruning, dendrite morphogenesis, and synaptic maturation and plasticity. In this review, we detail the nonproliferative postmitotic roles that these cell cycle proteins have recently been reported to play, the significance of their expression in neurons, mechanistic insight when available, and future prospects.
引用
收藏
页码:312 / 326
页数:15
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