The unfolded protein response is required for dendrite morphogenesis

被引:36
|
作者
Wei, Xing [1 ]
Howell, Audrey S. [1 ]
Dong, Xintong [1 ]
Taylor, Caitlin A. [1 ,2 ]
Cooper, Roshni C. [1 ]
Zhang, Jianqi [3 ]
Zou, Wei [4 ]
Sherwood, David R. [4 ]
Shen, Kang [1 ,2 ]
机构
[1] Stanford Univ, Howard Hughes Med Inst, Dept Biol, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Neurosci Program, Stanford, CA USA
[3] Univ So Calif, Dept Prevent Med, Div Biostat, Los Angeles, CA 90089 USA
[4] Duke Univ, Dept Biol, Durham, NC 27706 USA
来源
ELIFE | 2015年 / 4卷
基金
美国国家卫生研究院;
关键词
ENDOPLASMIC-RETICULUM STRESS; PLASMA-CELL DIFFERENTIATION; TRANSCRIPTION FACTOR XBP-1; CAENORHABDITIS-ELEGANS; C; ELEGANS; SELF-AVOIDANCE; DROSOPHILA DSCAM; MESSENGER-RNAS; PATHWAY; ARBORIZATION;
D O I
10.7554/eLife.06963
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Precise patterning of dendritic fields is essential for the formation and function of neuronal circuits. During development, dendrites acquire their morphology by exuberant branching. How neurons cope with the increased load of protein production required for this rapid growth is poorly understood. Here we show that the physiological unfolded protein response (UPR) is induced in the highly branched Caenorhabditis elegans sensory neuron PVD during dendrite morphogenesis. Perturbation of the IRE1 arm of the UPR pathway causes loss of dendritic branches, a phenotype that can be rescued by overexpression of the ER chaperone HSP-4 (a homolog of mammalian BiP/ grp78). Surprisingly, a single transmembrane leucine-rich repeat protein, DMA-1, plays a major role in the induction of the UPR and the dendritic phenotype in the UPR mutants. These findings reveal a significant role for the physiological UPR in the maintenance of ER homeostasis during morphogenesis of large dendritic arbors.
引用
收藏
页数:20
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