Evidence map›Paper›PMID 40585174›Full record

ArticlemedRxiv : the preprint server for health sciences2025

FUS Mislocalization Rewires a Cortical Gene Network to Drive Cognitive and Behavioral Impairment in ALS.

Raphaelle Cassel, Félicie Lorenc, Aurélie Bombardier, Claudia DE Tapia, Stéphane Dieterle, Cláudio Gouveia Roque, Christopher A Jackson, Geoffrey Stuart-Lopez, Caroline Rouaux, Simon J Guillot and 12 more

Abstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

22 authors.

Raphaelle CasselUniversité de Strasbourg, Inserm, Strasbourg Translational Neuroscience and Psychiatry, UMR-S1329, Centre de Recherches en Biomédecine; Strasbourg, France.
Félicie LorencUniversité de Strasbourg, Inserm, Strasbourg Translational Neuroscience and Psychiatry, UMR-S1329, Centre de Recherches en Biomédecine; Strasbourg, France.
Aurélie BombardierUniversité de Strasbourg, Inserm, Strasbourg Translational Neuroscience and Psychiatry, UMR-S1329, Centre de Recherches en Biomédecine; Strasbourg, France.
Claudia DE TapiaUniversité de Strasbourg, Inserm, Strasbourg Translational Neuroscience and Psychiatry, UMR-S1329, Centre de Recherches en Biomédecine; Strasbourg, France.
Stéphane DieterleUniversité de Strasbourg, Inserm, Strasbourg Translational Neuroscience and Psychiatry, UMR-S1329, Centre de Recherches en Biomédecine; Strasbourg, France.
Cláudio Gouveia RoqueCenter for Genomics of Neurodegenerative Disease, New York Genome Center, 101 Avenue of the Americas, New York, NY 10013, USA.
Christopher A JacksonCenter for Genomics of Neurodegenerative Disease, New York Genome Center, 101 Avenue of the Americas, New York, NY 10013, USA.
Geoffrey Stuart-LopezUniversité de Strasbourg, Inserm, Strasbourg Translational Neuroscience and Psychiatry, UMR-S1329, Centre de Recherches en Biomédecine; Strasbourg, France.
Caroline RouauxUniversité de Strasbourg, Inserm, Strasbourg Translational Neuroscience and Psychiatry, UMR-S1329, Centre de Recherches en Biomédecine; Strasbourg, France.ORCID 0000-0002-5724-2903
Simon J GuillotUniversité de Strasbourg, Inserm, Strasbourg Translational Neuroscience and Psychiatry, UMR-S1329, Centre de Recherches en Biomédecine; Strasbourg, France.ORCID 0000-0002-1623-7091
Marie-Christine BirlingPHENOMIN-Institut Clinique de la Souris, Université de Strasbourg, Illkirch, France.
Pascal KesslerUniversité de Strasbourg, INSERM, UMS 38, Imaging Core Facility PIC-STRA, CRBS, Strasbourg, France.
Maurizio GrassanoALS Center "Rita Levi Montalcini" Department of Neuroscience, University of Turin, Turin, Italy.
Bryan TraynorNeuromuscular Diseases Research Section, National Institute on Aging (NIA), National Institutes of Health (NIH), Bethesda, MD 20892, USA.
Adriano ChioALS Center "Rita Levi Montalcini" Department of Neuroscience, University of Turin, Turin, Italy.
Raju RoyDepartment of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104. U.S.A.
James ShorterDepartment of Biochemistry and Biophysics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA 19104. U.S.A.ORCID 0000-0001-5269-8533
Fergal M WaldronInstitute of Medical Sciences, University of Aberdeen, UK.
Jenna M GregoryInstitute of Medical Sciences, University of Aberdeen, UK.
Hemali PhatnaniCenter for Genomics of Neurodegenerative Disease, New York Genome Center, 101 Avenue of the Americas, New York, NY 10013, USA.
Luc DupuisUniversité de Strasbourg, Inserm, Strasbourg Translational Neuroscience and Psychiatry, UMR-S1329, Centre de Recherches en Biomédecine; Strasbourg, France.
Salim MegatUniversité de Strasbourg, Inserm, Strasbourg Translational Neuroscience and Psychiatry, UMR-S1329, Centre de Recherches en Biomédecine; Strasbourg, France.

Funding

Genome wide SNP analysis in Amyotrophic Lateral SclerosisZIAAG000933 · NIA · NATIONAL INSTITUTE ON AGING · PI TRAYNOR, BRYAN · 2009 to 2025
$9.8M
Intramural NIH HHS ZIA AG000933
6 · The paper itself

Abstract

Cognitive and behavioral impairment affects up to half of individuals with amyotrophic lateral sclerosis (ALS), but their molecular origin remains unresolved. Here, we identify mislocalization of the RNA-binding protein FUS in cortical neurons as a defining feature in ALS patients with cognitive impairment (ALS-ci). Selective mislocalization of FUS in adult cortical projection neurons in mice is sufficient to trigger ALS-ci- and ALS with behavioral impairment (ALS-bi)-like phenotypes, including deficits in sociability, and neurodegeneration. Single-nucleus transcriptomics reveal a conserved FUS-dependent gene network downregulated in these mice and ALS-ci patients. This regulon is enriched for ALS genetic risk factors and newly implicates

Indexed as

Amyotrophic lateral sclerosisbehavioral impairmentcognitive impairmentfronto-temporal dementiageneticsmouse modelssingle cell biology

Identifiers

PMID40585174
PMCPMC12204245

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Registered trials

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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.