Evidence map›Paper›PMID 41023182›Full record

ArticleScientific reports2025

The histone methyltransferase SETD2 regulates adult brain structure, connectivity and neurogenesis.

Cooper Atterton, Hallie Naumann, Benjamin Mitchell, Bee Meibusch, Laura Currey, Nyoman D Kurniawan, Stefan Thor, Michael Piper

Abstract read
In one paragraph

Article in Scientific reports, 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

8 authors.

Cooper AttertonThe School of Biomedical Sciences, Faculty of Health, Medicine and Behavioural Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
Hallie Naumann *The School of Biomedical Sciences, Faculty of Health, Medicine and Behavioural Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
Benjamin Mitchell *The School of Biomedical Sciences, Faculty of Health, Medicine and Behavioural Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
Bee MeibuschThe School of Biomedical Sciences, Faculty of Health, Medicine and Behavioural Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
Laura CurreyThe School of Biomedical Sciences, Faculty of Health, Medicine and Behavioural Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
Nyoman D KurniawanAustralian Institute for Bioengineering and Nanotechnology, Centre for Advanced Imaging, The University of Queensland, Brisbane, QLD, 4072, Australia.
Stefan ThorThe School of Biomedical Sciences, Faculty of Health, Medicine and Behavioural Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia.
Michael PiperThe School of Biomedical Sciences, Faculty of Health, Medicine and Behavioural Sciences, The University of Queensland, Brisbane, QLD, 4072, Australia. m.piper@uq.edu.au.

Funding

Australian Research Council DP220100985, DP230101750National Health and Medical Research Council 2019372
6 · The paper itself

Abstract

Epigenetic mechanisms are crucial for neocortical development. Recent work has highlighted that ablation of Setd2, which encodes a SET domain lysine methyltransferase, from the mouse dorsal telencephalon results in deficits in reciprocal cortico-thalamic connectivity. However, analysis of broader cortical phenotypes in this model has yet to be performed. Here, we addressed this, revealing that dorsal telencephalon-specific ablation of Setd2 results in decreased structural volumes across the entire adult brain, particularly within the hippocampus. Moreover, while homozygous Setd2-deficient brains exhibited apparently normal axonal integrity within the corpus callosum, axonal connections arising from the hippocampus were significantly impacted. Furthermore, whole brain structural connectivity was significantly altered in the absence of Setd2. Finally, we revealed structural, morphological and cellular changes within the hippocampal dentate gyrus of mutant mice. Collectively, these findings demonstrate a key role for SETD2 function in the development of the adult brain.

Indexed as

BrainHistone-Lysine N-MethyltransferaseNeurogenesisAnimalsAxonsCorpus CallosumDentate GyrusHippocampusMiceMice, KnockoutHistone-Lysine N-MethyltransferaseSETD2 protein, mouseAdult neurogenesisDT-MRIHippocampusLuscan-Lumish syndromeSETD2

Identifiers

PMID41023182
PMCPMC12480832

What OpenQuestion holds

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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.