Cell Reports
(Dec 2013)
Interactome of Two Diverse RNA Granules Links mRNA Localization to Translational Repression in Neurons
Renate Fritzsche,
Daniela Karra,
Keiryn L. Bennett,
Foong yee Ang,
Jacki E. Heraud-Farlow,
Marco Tolino,
Michael Doyle,
Karl E. Bauer,
Sabine Thomas,
Melanie Planyavsky,
Eric Arn,
Anetta Bakosova,
Kerstin Jungwirth,
Alexandra Hörmann,
Zsofia Palfi,
Julia Sandholzer,
Martina Schwarz,
Paolo Macchi,
Jacques Colinge,
Giulio Superti-Furga,
Michael A. Kiebler
Affiliations
Renate Fritzsche
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
Daniela Karra
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
Keiryn L. Bennett
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria
Foong yee Ang
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
Jacki E. Heraud-Farlow
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
Marco Tolino
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
Michael Doyle
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
Karl E. Bauer
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
Sabine Thomas
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
Melanie Planyavsky
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria
Eric Arn
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
Anetta Bakosova
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
Kerstin Jungwirth
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
Alexandra Hörmann
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
Zsofia Palfi
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
Julia Sandholzer
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
Martina Schwarz
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
Paolo Macchi
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
Jacques Colinge
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria
Giulio Superti-Furga
CeMM Research Center for Molecular Medicine of the Austrian Academy of Sciences, 1090 Vienna, Austria
Michael A. Kiebler
Department of Neuronal Cell Biology, Center for Brain Research, Medical University of Vienna, 1090 Vienna, Austria
DOI
https://doi.org/10.1016/j.celrep.2013.11.023
Journal volume & issue
Vol. 5,
no. 6
pp.
1749
– 1762
Abstract
Read online
Transport of RNAs to dendrites occurs in neuronal RNA granules, which allows local synthesis of specific proteins at active synapses on demand, thereby contributing to learning and memory. To gain insight into the machinery controlling dendritic mRNA localization and translation, we established a stringent protocol to biochemically purify RNA granules from rat brain. Here, we identified a specific set of interactors for two RNA-binding proteins that are known components of neuronal RNA granules, Barentsz and Staufen2. First, neuronal RNA granules are much more heterogeneous than previously anticipated, sharing only a third of the identified proteins. Second, dendritically localized mRNAs, e.g., Arc and CaMKIIα, associate selectively with distinct RNA granules. Third, our work identifies a series of factors with known roles in RNA localization, translational control, and RNA quality control that are likely to keep localized transcripts in a translationally repressed state, often in distinct types of RNPs.
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