Many different types of polarized eukaryotic cells have been shown to segregate synthesis for some protein subpopulations to cytoplasmic domains distant from their nucleus. For neurons, these distances can be tens-to-thousands fold more than the diameter of the cell body. Both axons and dendrites make use of this localized protein synthesis to bring autonomy to these far reaches of the cytoplasm (Gomes et al., 2014). This local mRNA translation is often used to mount a rapid response to extracellular stimuli encountered by the distal axon and dendrite. Indeed, activating translation of mRNAs residing locally at the synapse or growth cone brings a much more rapid response than could be achieved by transporting new proteins from the cell body. The neuron likely reaps a cost benefit from this mechanism in terms of energy consumption, since multiple protein copies can be generated from a single mRNA through sequential rounds of translation. Localized protein synthesis could also more effectively position a protein near its site of action or even bring an unanticipated novel function to the protein.
Old dogs with new tricks: intra-axonal translation of nuclear proteins
Creators
Jeffery L. Twiss - Drexel University
Tanuja T. Merianda - Drexel University
Publication Details
Neural regeneration research, v 10(10), pp 1560-1562
Publisher
MEDKNOW PUBLICATIONS & MEDIA PVT LTD
Number of pages
3
Grant note
R01 NS041596 / NINDS NIH HHS; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Neurological Disorders & Stroke (NINDS)
Resource Type
Editorial
Language
English
Academic Unit
Neurobiology and Anatomy
Web of Science ID
WOS:000364260700009
Scopus ID
2-s2.0-84945564298
Other Identifier
991021892011104721
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Collaboration types
Domestic collaboration
Web of Science research areas
Cell Biology
Neurosciences
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