Evidence map›Paper›PMID 39259737›Full record

ArticlePLoS genetics2024

Direct targets of MEF2C are enriched for genes associated with schizophrenia and cognitive function and are involved in neuron development and mitochondrial function.

Deema Ali, Aodán Laighneach, Emma Corley, Saahithh Redddi Patlola, Rebecca Mahoney, Laurena Holleran, Declan P McKernan, John P Kelly, Aiden P Corvin, Brian Hallahan and 3 more

Abstract read
In one paragraph

Article in PLoS genetics, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Review
  5. Article
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

13 authors.

Deema AliCentre for Neuroimaging, Cognition and Genomics (NICOG), University of Galway, Ireland.
Aodán LaighneachCentre for Neuroimaging, Cognition and Genomics (NICOG), University of Galway, Ireland.ORCID 0000-0003-4853-8953
Emma CorleyCentre for Neuroimaging, Cognition and Genomics (NICOG), University of Galway, Ireland.
Saahithh Redddi PatlolaCentre for Neuroimaging, Cognition and Genomics (NICOG), University of Galway, Ireland.ORCID 0000-0003-4367-1720
Rebecca MahoneyCentre for Neuroimaging, Cognition and Genomics (NICOG), University of Galway, Ireland.
Laurena HolleranCentre for Neuroimaging, Cognition and Genomics (NICOG), University of Galway, Ireland.
Declan P McKernanDiscipline of Pharmacology & Therapeutics, School of Medicine, University of Galway, Ireland.ORCID 0000-0002-9691-1671
John P KellyDiscipline of Pharmacology & Therapeutics, School of Medicine, University of Galway, Ireland.
Aiden P CorvinNeuropsychiatric Genetics Research Group, Department of Psychiatry, Trinity College Dublin, Ireland.
Brian HallahanCentre for Neuroimaging, Cognition and Genomics (NICOG), University of Galway, Ireland.
Colm McDonaldCentre for Neuroimaging, Cognition and Genomics (NICOG), University of Galway, Ireland.ORCID 0000-0003-1661-5192
Gary DonohoeCentre for Neuroimaging, Cognition and Genomics (NICOG), University of Galway, Ireland.
Derek W MorrisCentre for Neuroimaging, Cognition and Genomics (NICOG), University of Galway, Ireland.ORCID 0000-0002-3413-570X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Myocyte Enhancer Factor 2C (MEF2C) is a transcription factor that plays a crucial role in neurogenesis and synapse development. Genetic studies have identified MEF2C as a gene that influences cognition and risk for neuropsychiatric disorders, including autism spectrum disorder (ASD) and schizophrenia (SCZ). Here, we investigated the involvement of MEF2C in these phenotypes using human-derived neural stem cells (NSCs) and glutamatergic induced neurons (iNs), which represented early and late neurodevelopmental stages. For these cellular models, MEF2C function had previously been disrupted, either by direct or indirect mutation, and gene expression assayed using RNA-seq. We integrated these RNA-seq data with MEF2C ChIP-seq data to identify dysregulated direct target genes of MEF2C in the NSCs and iNs models. Several MEF2C direct target gene-sets were enriched for SNP-based heritability for intelligence, educational attainment and SCZ, as well as being enriched for genes containing rare de novo mutations reported in ASD and/or developmental disorders. These gene-sets are enriched in both excitatory and inhibitory neurons in the prenatal and adult brain and are involved in a wide range of biological processes including neuron generation, differentiation and development, as well as mitochondrial function and energy production. We observed a trans expression quantitative trait locus (eQTL) effect of a single SNP at MEF2C (rs6893807, which is associated with IQ) on the expression of a target gene, BNIP3L. BNIP3L is a prioritized risk gene from the largest genome-wide association study of SCZ and has a function in mitophagy in mitochondria. Overall, our analysis reveals that either direct or indirect disruption of MEF2C dysregulates sets of genes that contain multiple alleles associated with SCZ risk and cognitive function and implicates neuron development and mitochondrial function in the etiology of these phenotypes.

Indexed as

CognitionMEF2 Transcription FactorsNeurogenesisSchizophreniaAutism Spectrum DisorderGenome-Wide Association StudyHumansMitochondriaNeural Stem CellsNeuronsPolymorphism, Single NucleotideMEF2C protein, humanMEF2 Transcription Factors

Identifiers

PMID39259737
PMCPMC11419381

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.