Evidence map›Paper›PMID 27181636›Full record

ArticleScientific reports2016

Usp9x-deficiency disrupts the morphological development of the postnatal hippocampal dentate gyrus.

Sabrina Oishi, Susitha Premarathne, Tracey J Harvey, Swati Iyer, Chantelle Dixon, Suzanne Alexander, Thomas H J Burne, Stephen A Wood, Michael Piper

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.4field-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

25 citing papers in PubMed, 33 citations in OpenAlex.

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  10. Protein clearance strategies for disease intervention.Journal of neural transmission (Vienna, Austria : 1996) · 2022
    Review
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  18. Whole-exome sequencing reveals novelClinical case reports · 2019
    Article
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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

9 authors at 4 institutions in 1 country.

Sabrina OishiThe School of Biomedical Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
Susitha PremarathneThe Eskitis Institute for Drug Discovery, Griffith University, Brisbane, QLD, 4111, Australia.
Tracey J HarveyThe School of Biomedical Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
Swati IyerThe School of Biomedical Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
Chantelle DixonThe School of Biomedical Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
Suzanne AlexanderQueensland Centre for Mental Health Research, The Park Centre for Mental Health, Richlands, QLD, 4077, Australia.
Thomas H J BurneQueensland Centre for Mental Health Research, The Park Centre for Mental Health, Richlands, QLD, 4077, Australia.
Stephen A WoodThe Eskitis Institute for Drug Discovery, Griffith University, Brisbane, QLD, 4111, Australia.
Michael PiperThe School of Biomedical Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
University of Queensland · AUGriffith University · AUPark Centre for Mental Health · AUQueensland Centre for Mental Health Research · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Within the adult mammalian brain, neurogenesis persists within two main discrete locations, the subventricular zone lining the lateral ventricles, and the hippocampal dentate gyrus. Neurogenesis within the adult dentate gyrus contributes to learning and memory, and deficiencies in neurogenesis have been linked to cognitive decline. Neural stem cells within the adult dentate gyrus reside within the subgranular zone (SGZ), and proteins intrinsic to stem cells, and factors within the niche microenvironment, are critical determinants for development and maintenance of this structure. Our understanding of the repertoire of these factors, however, remains limited. The deubiquitylating enzyme USP9X has recently emerged as a mediator of neural stem cell identity. Furthermore, mice lacking Usp9x exhibit a striking reduction in the overall size of the adult dentate gyrus. Here we reveal that the development of the postnatal SGZ is abnormal in mice lacking Usp9x. Usp9x conditional knockout mice exhibit a smaller hippocampus and shortened dentate gyrus blades from as early as P7. Moreover, the analysis of cellular populations within the dentate gyrus revealed reduced stem cell, neuroblast and neuronal numbers and abnormal neuroblast morphology. Collectively, these findings highlight the critical role played by USP9X in the normal morphological development of the postnatal dentate gyrus.

Indexed as

AnimalsAnimals, NewbornCell CountCell DifferentiationDentate GyrusEndopeptidasesFemaleIntegrasesMiceNeural Stem CellsOrgan SizeUbiquitin ThiolesteraseCre recombinaseEndopeptidasesIntegrasesUbiquitin ThiolesteraseUsp9x protein, mouse

Identifiers

PMID27181636
PMCPMC4867638
OpenAlexW2395949678

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.