Evidence map›Paper›PMID 31092554›Full record

ArticleThe Journal of biological chemistry2019

The RNA-binding protein FUS/TLS undergoes calcium-mediated nuclear egress during excitotoxic stress and is required for

Maeve Tischbein, Desiree M Baron, Yen-Chen Lin, Katherine V Gall, John E Landers, Claudia Fallini, Daryl A Bosco

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 30 citations in OpenAlex.

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  15. Frontiers in physiology · 2021
    Article
  16. FUS contributes to mTOR-dependent inhibition of translation.The Journal of biological chemistry · 2020
    Article
  17. Review
  18. Phenotypic Suppression of ALS/FTD-Associated Neurodegeneration Highlights Mechanisms of Dysfunction.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Review
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

7 authors at 1 institution in 1 country.

Maeve TischbeinFrom the Department of Neurology, University of Massachusetts Medical School, Worcester, Massachusetts 01605.ORCID 0000-0003-1192-0673
Desiree M BaronFrom the Department of Neurology, University of Massachusetts Medical School, Worcester, Massachusetts 01605.
Yen-Chen LinFrom the Department of Neurology, University of Massachusetts Medical School, Worcester, Massachusetts 01605.
Katherine V GallFrom the Department of Neurology, University of Massachusetts Medical School, Worcester, Massachusetts 01605.
John E LandersFrom the Department of Neurology, University of Massachusetts Medical School, Worcester, Massachusetts 01605.
Claudia FalliniFrom the Department of Neurology, University of Massachusetts Medical School, Worcester, Massachusetts 01605.
Daryl A BoscoFrom the Department of Neurology, University of Massachusetts Medical School, Worcester, Massachusetts 01605 Daryl.Bosco@umassmed.edu.
University of Massachusetts Chan Medical School · US

Funding

Characterization of KIFAP3, a Modifier of Survival in Sporadic ALSR01NS065847 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI LANDERS, JOHN E · 2010 to 2014
$1.8M
Investigating a Toxic Gain-of-Interaction Between FUS/TLS & Stress GranulesR01NS078145 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BOSCO, DARYL ANGELA · 2012 to 2016
$1.8M
Investigating the response of FUS/TLS to excitotoxic insultR21NS091860 · NINDS · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI BOSCO, DARYL ANGELA · 2015 to 2016
$461k
NINDS NIH HHS R01 NS065847NINDS NIH HHS R01 NS078145NINDS NIH HHS R21 NS091860
6 · The paper itself

Abstract

Excitotoxic levels of glutamate represent a physiological stress that is strongly linked to amyotrophic lateral sclerosis (ALS) and other neurological disorders. Emerging evidence indicates a role for neurodegenerative disease-linked RNA-binding proteins (RBPs) in the cellular stress response. However, the relationships between excitotoxicity, RBP function, and disease have not been explored. Here, using primary cortical and motor neurons, we found that excitotoxicity induced the translocation of select ALS-linked RBPs from the nucleus to the cytoplasm within neurons. RBPs affected by excitotoxicity included TAR DNA-binding protein 43 (TDP-43) and, most robustly, fused in sarcoma/translocated in liposarcoma (FUS/TLS or FUS). We noted that FUS is translocated through a calcium-dependent mechanism and that its translocation coincides with striking alterations in nucleocytoplasmic transport. Furthermore, glutamate-induced up-regulation of glutamate ionotropic receptor α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA)-type subunit 2 (

Indexed as

Stress, PhysiologicalActive Transport, Cell NucleusAmyotrophic Lateral SclerosisCalciumCell NucleusCytoplasmFrontotemporal DementiaGlutamic AcidHumansMutationNeuronsReceptors, AMPARNA-Binding Protein FUSRNA, MessengerRNA Processing, Post-TranscriptionalCalciumFUS protein, humanglutamate receptor ionotropic, AMPA 2Glutamic AcidReceptors, AMPARNA-Binding Protein FUSRNA, Messengeramyotrophic lateral sclerosis (ALS) (Lou Gehrig disease)excitatory neurotransmissionexcitotoxicityfused in sarcoma/translocated in liposarcoma (FUS/TLS)glutamateglutamate ionotropic receptor AMPA type subunit 2 (Gria2)glutamate receptor 2 (GluA2)neurodegenerationnucleocytoplasmic transportRNA transport

Identifiers

PMID31092554
PMCPMC6664169
OpenAlexW2946687314

What OpenQuestion holds

Textmetadata
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.