Evidence map›Paper›PMID 31813652›Full record

ArticleNeuron2020

Usp9X Controls Ankyrin-Repeat Domain Protein Homeostasis during Dendritic Spine Development.

Sehyoun Yoon, Euan Parnell, Maria Kasherman, Marc P Forrest, Kristoffer Myczek, Susitha Premarathne, Michelle C Sanchez Vega, Michael Piper, Thomas H J Burne, Lachlan A Jolly and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Neuron, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
2.2field-weighted citation impact, top 11% 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

39 citing papers in PubMed, 72 citations in OpenAlex.

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  13. Ubiquitin system mutations in neurological diseases.Trends in biochemical sciences · 2024
    Review
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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

12 authors at 4 institutions in 2 countries.

Sehyoun YoonDepartment of Physiology, Northwestern University Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Euan ParnellDepartment of Physiology, Northwestern University Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Maria KashermanGriffith Institute for Drug Discovery, Griffith University, Brisbane, QLD 4111, Australia; The School of Biomedical Sciences, The University of Queensland, Brisbane, QLD 4072 Australia.
Marc P ForrestDepartment of Physiology, Northwestern University Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Kristoffer MyczekDepartment of Physiology, Northwestern University Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA.
Susitha PremarathneGriffith Institute for Drug Discovery, Griffith University, Brisbane, QLD 4111, Australia.
Michelle C Sanchez VegaQueensland Brain Institute, The University of Queensland, Brisbane, QLD 4072, Australia.
Michael PiperThe School of Biomedical Sciences, The University of Queensland, Brisbane, QLD 4072 Australia; Queensland Brain Institute, The University of Queensland, Brisbane, QLD 4072, Australia.
Thomas H J BurneQueensland Brain Institute, The University of Queensland, Brisbane, QLD 4072, Australia; Queensland Centre for Mental Health Research, The Park Centre for Mental Health, Wacol, QLD 4076, Australia.
Lachlan A JollyRobinson Research Institute, School of Medicine, University of Adelaide, Adelaide, SA 5005, Australia.
Stephen A WoodGriffith Institute for Drug Discovery, Griffith University, Brisbane, QLD 4111, Australia.
Peter PenzesDepartment of Physiology, Northwestern University Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA; Department of Psychiatry and Behavioral Sciences, Northwestern University Feinberg School of Medicine, Northwestern University, Chicago, IL 60611, USA. Electronic address: p-penzes@northwestern.edu.
Northwestern University · USUniversity of Queensland · AUGriffith University · AUUniversity of Adelaide · AU

Funding

Postsynaptic roles of ankyrinsR01MH107182 · NIMH · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Peter Penzes · 2015 to 2026
$5.6M
NIMH NIH HHS R01 MH107182
6 · The paper itself

Abstract

Variants in the ANK3 gene encoding ankyrin-G are associated with neurodevelopmental disorders, including intellectual disability, autism, schizophrenia, and bipolar disorder. However, no upstream regulators of ankyrin-G at synapses are known. Here, we show that ankyrin-G interacts with Usp9X, a neurodevelopmental-disorder-associated deubiquitinase (DUB). Usp9X phosphorylation enhances their interaction, decreases ankyrin-G polyubiquitination, and stabilizes ankyrin-G to maintain dendritic spine development. In forebrain-specific Usp9X knockout mice (Usp9X

Indexed as

AnimalsAnkyrin RepeatCells, CulturedDendritic SpinesHEK293 CellsHomeostasisHumansMaleMiceMice, Inbred C57BLMice, KnockoutNeurogenesisProtein Structure, SecondaryProtein Structure, TertiaryProteostasisUbiquitin ThiolesteraseUbiquitin ThiolesteraseUsp9x protein, mouseANKankyrin-Gdeubiquitinaseintellectual disabilityproximity ligation assaySHANKstructured illumination microscopy

Identifiers

PMID31813652
PMCPMC7007386
OpenAlexW2993815951

What OpenQuestion holds

Textmetadata
LicenceTDM
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.