Drosophila CLASP regulates microtubule orientation and dendrite pruning by suppressing Par-1 kinase

被引:4
作者
Bu, Shufeng [1 ,2 ]
Tang, Quan [1 ]
Wang, Yan [1 ]
Lau, Samuel Song Yuan [1 ]
Yong, Wei Lin [1 ]
Wu, Fengwei [1 ,2 ]
机构
[1] Natl Univ Singapore, Temasek Life Sci Lab, Res Link 1, Singapore, Singapore
[2] Natl Univ Singapore, Dept Biol Sci, Singapore, Singapore
来源
CELL REPORTS | 2022年 / 39卷 / 09期
基金
新加坡国家研究基金会;
关键词
NEURITE OUTGROWTH; BINDING PROTEIN; TOG-DOMAIN; AXON; POLARITY; DYNAMICS; NEURONS; TRACKING; NETWORK; FAMILY;
D O I
10.1016/j.celrep.2022.110887
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The evolutionarily conserved CLASPs (cytoplasmic linker-associated proteins) are microtubule-associated proteins that inhibit microtubule catastrophe and promote rescue. CLASPs can regulate axonal elongation and dendrite branching in growing neurons. However, their roles in microtubule orientation and neurite pruning in remodeling neurons remain unknown. Here, we identify the Drosophila CLASP homolog Orbit/MAST, which is required for dendrite pruning in ddaC sensory neurons during metamorphosis. Orbit is important for maintenance of the minus-end-out microtubule orientation in ddaC dendrites. Our structural analysis reveals that the microtubule lattice-binding TOG2 domain is required for Orbit to regulate dendritic microtubule orientation and dendrite pruning. In a genetic modifier screen, we further identify the conserved Par-1 kinase as a suppressor of Orbit in dendritic microtubule orientation. Moreover, elevated Par-1 function impairs dendritic microtubule orientation and dendrite pruning, phenocopying orbit mutants. Overall, our study demonstrates that Drosophila CLASP governs dendritic microtubule orientation and dendrite pruning at least partly via suppressing Par-1 kinase.
引用
收藏
页数:19
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