Evidence map›Paper›PMID 27462983›Full record

ArticlePLoS genetics2016

Tracking the Fragile X Mental Retardation Protein in a Highly Ordered Neuronal RiboNucleoParticles Population: A Link between Stalled Polyribosomes and RNA Granules.

Rachid El Fatimy, Laetitia Davidovic, Sandra Tremblay, Xavier Jaglin, Alain Dury, Claude Robert, Paul De Koninck, Edouard W Khandjian

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed
8.1field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

58 citing papers in PubMed, 115 citations in OpenAlex.

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  8. FMR1 KH0-KH1 domains coordinate mExperimental cell research · 2025
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  18. Puromycin reveals a distinct conformation of neuronal ribosomes.Proceedings of the National Academy of Sciences of the United States of America · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 3 countries.

Rachid El FatimyInstitut universitaire en santé mentale de Québec, Quebec, Canada.
Laetitia DavidovicInstitut de Pharmacologie Moléculaire et Cellulaire, UMR7275, Université de Nice-Sophia Antipolis, F-06560 Valbonne, France.
Sandra TremblayInstitut universitaire en santé mentale de Québec, Quebec, Canada.
Xavier JaglinNeuroscience Institute, Department of Neuroscience and Physiology, New York University, New York, New York, United States of America.
Alain DuryInstitut universitaire en santé mentale de Québec, Quebec, Canada.
Claude RobertCentre de recherche en biologie de la reproduction, Département des sciences animales, Faculté des sciences de l'agriculture et de l'alimentation, Université Laval, Québec, Quebec, Canada.
Paul De KoninckInstitut universitaire en santé mentale de Québec, Quebec, Canada.
Edouard W KhandjianInstitut universitaire en santé mentale de Québec, Quebec, Canada.
Institut Universitaire en Santé Mentale de Québec · CAUniversité Laval · CAInstitut de Pharmacologie Moléculaire et Cellulaire · FRNeurosciences Institute · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Local translation at the synapse plays key roles in neuron development and activity-dependent synaptic plasticity. mRNAs are translocated from the neuronal soma to the distant synapses as compacted ribonucleoparticles referred to as RNA granules. These contain many RNA-binding proteins, including the Fragile X Mental Retardation Protein (FMRP), the absence of which results in Fragile X Syndrome, the most common inherited form of intellectual disability and the leading genetic cause of autism. Using FMRP as a tracer, we purified a specific population of RNA granules from mouse brain homogenates. Protein composition analyses revealed a strong relationship between polyribosomes and RNA granules. However, the latter have distinct architectural and structural properties, since they are detected as close compact structures as observed by electron microscopy, and converging evidence point to the possibility that these structures emerge from stalled polyribosomes. Time-lapse video microscopy indicated that single granules merge to form cargoes that are transported from the soma to distal locations. Transcriptomic analyses showed that a subset of mRNAs involved in cytoskeleton remodelling and neural development is selectively enriched in RNA granules. One third of the putative mRNA targets described for FMRP appear to be transported in granules and FMRP is more abundant in granules than in polyribosomes. This observation supports a primary role for FMRP in granules biology. Our findings open new avenues for the study of RNA granule dysfunctions in animal models of nervous system disorders, such as Fragile X syndrome.

Indexed as

AnimalsBrainFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeGene Expression Regulation, DevelopmentalHumansMiceNeuronal PlasticityNeuronsPolyribosomesProtein BiosynthesisRNA-Binding ProteinsRNA, MessengerSynapsesFragile X Messenger Ribonucleoprotein 1RNA-Binding ProteinsRNA, Messenger

Identifiers

PMID27462983
PMCPMC4963131
OpenAlexW2505019684

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.