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  Live cell imaging reveals 3′-UTR dependent mRNA sorting to synapses

Bauer, K. E., Segura, I., Gaspar, I., Scheuss, V., IIlig, C., Ammer, G., et al. (2019). Live cell imaging reveals 3′-UTR dependent mRNA sorting to synapses. Nature Communications, 10: 3178. doi:10.1038/s41467-019-11123-x.

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 Creators:
Bauer, Karl E., Author
Segura, Inmaculada1, Author           
Gaspar, Imre, Author
Scheuss, Volker, Author
IIlig, Christin, Author
Ammer, Georg2, Author           
Hutten, Saskia, Author
Basyuk, Eugenia, Author
Fernandez-Moya, Sandra M., Author
Ehses, Janina, Author
Bertrand, Edouard, Author
Kiebler, Michael A., Author
Affiliations:
1Ludwig-Maximilians-Universität München, External Organizations, Geschwister-Scholl-Platz 1, 80539 München, DE, ou_3346850              
2Department: Circuits-Computation-Models / Borst, MPI of Neurobiology, Max Planck Society, ou_1113548              

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Free keywords: INTRACELLULAR-LOCALIZATION; RIBONUCLEOPROTEIN COMPLEX; LOCAL TRANSLATION; GENE-EXPRESSION; TRANSPORT; PROTEIN; DYNAMICS; STAUFEN; NEURONS; VISUALIZATIONScience & Technology - Other Topics;
 Abstract: mRNA transport restricts translation to specific subcellular locations, which is the basis for many cellular functions. However, the precise process of mRNA sorting to synapses in neurons remains elusive. Here we use Rgs4 mRNA to investigate 3'-UTR-dependent transport by MS2 live-cell imaging. The majority of observed RNA granules display 3'-UTR independent bidirectional transport in dendrites. Importantly, the Rgs4 3'-UTR causes an anterograde transport bias, which requires the Staufen2 protein. Moreover, the 3'-UTR mediates dynamic, sustained mRNA recruitment to synapses. Visualization at high temporal resolution enables us to show mRNA patrolling dendrites, allowing transient interaction with multiple synapses, in agreement with the sushi-belt model. Modulation of neuronal activity by either chemical silencing or local glutamate uncaging regulates both the 3'-UTR-dependent transport bias and synaptic recruitment. This dynamic and reversible mRNA recruitment to active synapses would allow translation and synaptic remodeling in a spatially and temporally adaptive manner.

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Language(s): eng - English
 Dates: 2019-07-18
 Publication Status: Issued
 Pages: 13
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 Rev. Type: Peer
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Project name : SFB870
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Title: Nature Communications
  Abbreviation : Nat. Commun.
Source Genre: Journal
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Publ. Info: London : Nature Publishing Group
Pages: - Volume / Issue: 10 Sequence Number: 3178 Start / End Page: - Identifier: ISSN: 2041-1723
CoNE: https://pure.mpg.de/cone/journals/resource/2041-1723