TDP-43 Regulates Coupled Dendritic mRNA Transport-Translation Processes in Co-operation with FMRP and Staufen1

被引:58
作者
Chu, Jen-Fei [1 ]
Majumder, Pritha [1 ]
Chatterjee, Biswanath [1 ]
Huang, Shih-Ling [1 ]
Shen, Che-Kun James [1 ]
机构
[1] Acad Sinica, Inst Mol Biol, Taipei 115, Taiwan
来源
CELL REPORTS | 2019年 / 29卷 / 10期
关键词
LOCAL TRANSLATION; PROTEIN; NEURONS; DYNEIN; LIVE; LOCALIZATION; DYNAMICS; KINESIN; CELLS; ALS;
D O I
10.1016/j.celrep.2019.10.061
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Tightly regulated transport of messenger ribonucleoprotein (mRNP) granules to diverse locations of dendrites and axons is essential for appropriately timed protein synthesis within distinct sub-neuronal compartments. Perturbations of this regulation lead to various neurological disorders. Using imaging and molecular approaches, we demonstrate how TDP-43 co-operates with two other RNA-binding proteins, FMRP and Staufen1 , to regulate the anterograde and retrograde transport, respectively, of Rac1 mRNPs in mouse neuronal dendrites. We also analyze the mechanisms by which TDP-43 mediates coupled mRNA transport-translation processes in dendritic sub-compartments by following in real-time the co-movement of RNA and endogenous fluorescence-tagged protein in neurons and by simultaneous examination of transport/translation dynamics by using an RNA biosensor. This study establishes the pivotal roles of TDP-43 in transporting mRNP granules in dendrites, inhibiting translation inside those granules, and reactivating it once the granules reach the dendritic spines.
引用
收藏
页码:3118 / +
页数:22
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