Receptor-specific interactome as a hub for rapid cue-induced selective translation in axons

被引:43
作者
Koppers, Max [1 ]
Cagnetta, Roberta [1 ]
Shigeoka, Toshiaki [1 ]
Wunderlich, Lucia C. S. [2 ]
Vallejo-Ramirez, Pedro [2 ]
Lin, Julie Qiaojin [1 ]
Zhao, Sixian [1 ]
Jakobs, Maximilian A. H. [1 ]
Dwivedy, Asha [1 ,2 ]
Minett, Michael S. [1 ]
Bellon, Anais [1 ]
Kaminski, Clemens F. [2 ]
Harris, William A. [1 ]
Flanagan, John G. [3 ]
Holt, Christine E. [1 ]
机构
[1] Univ Cambridge, Dept Physiol Dev & Neurosci, Cambridge, England
[2] Univ Cambridge, Dept Chem Engn & Biotechnol, Cambridge, England
[3] Harvard Med Sch, Dept Cell Biol, Boston, MA 02115 USA
基金
英国工程与自然科学研究理事会; 欧洲研究理事会; 英国惠康基金; 芬兰科学院;
关键词
LOCAL PROTEIN-SYNTHESIS; MESSENGER-RNA LOCALIZATION; BINDING-PROTEIN; CHEMOTROPIC RESPONSES; SIGNALING MECHANISMS; GROWTH; GUIDANCE; COLLAPSE; PHOSPHORYLATION; INTEGRATION;
D O I
10.7554/eLife.48718
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Extrinsic cues trigger the local translation of specific mRNAs in growing axons via cell surface receptors. The coupling of ribosomes to receptors has been proposed as a mechanism linking signals to local translation but it is not known how broadly this mechanism operates, nor whether it can selectively regulate mRNA translation. We report that receptor-ribosome coupling is employed by multiple guidance cue receptors and this interaction is mRNA-dependent. We find that different receptors associate with distinct sets of mRNAs and RNA-binding proteins. Cue stimulation of growing Xenopus retinal ganglion cell axons induces rapid dissociation of ribosomes from receptors and the selective translation of receptor-specific mRNAs. Further, we show that receptor-ribosome dissociation and cue-induced selective translation are inhibited by co-exposure to translation-repressive cues, suggesting a novel mode of signal integration. Our findings reveal receptor-specific interactomes and suggest a generalizable model for cue-selective control of the local proteome.
引用
收藏
页数:27
相关论文
共 59 条
[1]  
[Anonymous], 1994, NORMAL TABLE XENOPUS
[2]   FMRP targets distinct mRNA sequence elements to regulate protein expression [J].
Ascano, Manuel, Jr. ;
Mukherjee, Neelanjan ;
Bandaru, Pradeep ;
Miller, Jason B. ;
Nusbaum, Jeffrey D. ;
Corcoran, David L. ;
Langlois, Christine ;
Munschauer, Mathias ;
Dewell, Scott ;
Hafner, Markus ;
Williams, Zev ;
Ohler, Uwe ;
Tuschl, Thomas .
NATURE, 2012, 492 (7429) :382-+
[3]   miR-182 Regulates Slit2-Mediated Axon Guidance by Modulating the Local Translation of a Specific mRNA [J].
Bellon, Anais ;
Iyer, Archana ;
Bridi, Simone ;
Lee, Flora C. Y. ;
Ovando-Vazquez, Cesare ;
Corradi, Eloina ;
Longhi, Sara ;
Roccuzzo, Michela ;
Strohbuecker, Stephanie ;
Naik, Sindhu ;
Sarkies, Peter ;
Miska, Eric ;
Abreu-Goodger, Cei ;
Holt, Christine E. ;
Baudet, Marie-Laure .
CELL REPORTS, 2017, 18 (05) :1171-1186
[4]   Noncanonical Modulation of the eIF2 Pathway Controls an Increase in Local Translation during Neural Wiring [J].
Cagnetta, Roberta ;
Wong, Hovy Ho-Wai ;
Frese, Christian K. ;
Mallucci, Giovanna R. ;
Krijgsveld, Jeroen ;
Holt, Christine E. .
MOLECULAR CELL, 2019, 73 (03) :474-+
[5]   Rapid Cue-Specific Remodeling of the Nascent Axonal Proteome [J].
Cagnetta, Roberta ;
Frese, Christian K. ;
Shigeoka, Toshiaki ;
Krijgsveld, Jeroen ;
Holt, Christine E. .
NEURON, 2018, 99 (01) :29-+
[6]   Apoptotic pathway and MAPKs differentially regulate chemotropic responses of retinal growth cones [J].
Campbell, DS ;
Holt, CE .
NEURON, 2003, 37 (06) :939-952
[7]   Chemotropic responses of retinal growth cones mediated by rapid local protein synthesis and degradation [J].
Campbell, DS ;
Holt, CE .
NEURON, 2001, 32 (06) :1013-1026
[8]   Semaphorin 3A elicits stage-dependent collapse, turning, and branching in Xenopus retinal growth cones [J].
Campbell, DS ;
Regan, AG ;
Lopez, JS ;
Tannahill, D ;
Harris, WA ;
Holt, CE .
JOURNAL OF NEUROSCIENCE, 2001, 21 (21) :8538-8547
[9]   Expansion microscopy [J].
Chen, Fei ;
Tillberg, Paul W. ;
Boyden, Edward S. .
SCIENCE, 2015, 347 (6221) :543-548
[10]   Late Endosomes Act as mRNA Translation Platforms and Sustain Mitochondria in Axons [J].
Cioni, Jean-Michel ;
Lin, Julie Qiaojin ;
Holtermann, Anne V. ;
Koppers, Max ;
Jakobs, Maximilian A. H. ;
Azizi, Afnan ;
Turner-Bridger, Benita ;
Shigeoka, Toshiaki ;
Franze, Kristian ;
Harris, William A. ;
Holt, Christine E. .
CELL, 2019, 176 (1-2) :56-+