Evidence map›Paper›PMID 41253765›Full record

ArticleTranslational psychiatry2025

A non-coding RNA risk pathway in schizophrenia: miR-137 enhances the lncRNA GOMAFU through a pathological transcription network.

Peng Teng, Ying Zhou, Xingyu Ji, Yangping Li, Li Ku, Feng Wang, Zhexing Wen, Bing Yao, Yue Feng

Abstract read
In one paragraph

Article in Translational psychiatry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

9 authors.

Peng Teng *Department of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, USA.
Ying Zhou *Psychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA.
Xingyu Ji *Department of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, USA.
Yangping LiHuman Genetics, Emory University School of Medicine, Atlanta, GA, USA.
Li KuDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, USA.
Feng WangHuman Genetics, Emory University School of Medicine, Atlanta, GA, USA.
Zhexing WenPsychiatry and Behavioral Sciences, Emory University School of Medicine, Atlanta, GA, USA. zhexing.wen@emory.edu.ORCID http://orcid.org/0000-0002-1518-3845
Bing YaoHuman Genetics, Emory University School of Medicine, Atlanta, GA, USA. bing.yao@emory.edu.ORCID http://orcid.org/0000-0002-3205-8130
Yue FengDepartment of Pharmacology and Chemical Biology, Emory University School of Medicine, Atlanta, GA, USA. yfeng@emory.edu.ORCID http://orcid.org/0000-0002-7905-2182

Funding

Towards a better understanding of genetic architecture of Alzheimer's disease with human iPSC modelsR01AG065611 · NIA · EMORY UNIVERSITY · PI LI, BINGSHAN, WEN, ZHEXING · 2020 to 2024
$3.8M
Elucidating the Roles of Transposable Elements in Alzheimer's and related dementiasR01AG078937 · NIA · EMORY UNIVERSITY · PI PENG JIN, Bing Yao · 2022 to 2026
$3.7M
Genome-wide mapping and integrative analysis of DNA 6mA methylome in human AD brainR01AG064786 · NIA · UNIVERSITY OF FLORIDA · PI BENNETT, DAVID ALAN, YAO, BING · 2019 to 2023
$3.3M
Novel Regulation and Function of the lncRNA Gomafu in Human NeuronsR01NS110110 · NINDS · EMORY UNIVERSITY · PI FENG, YUE · 2019 to 2023
$2.9M
Regulation and function of human neural circular RNAsR01NS118819 · NINDS · EMORY UNIVERSITY · PI FENG, YUE, YAO, BING · 2021 to 2025
$2.7M
Epigenetic roles of DNA adenine methylation in stress responseR01MH117122 · NIMH · EMORY UNIVERSITY · PI YAO, BING · 2019 to 2023
$2.0M
Epigenetic roles of DNA adenine methylation in Alzheimer's DiseaseR01AG062577 · NIA · EMORY UNIVERSITY · PI YAO, BING · 2019 to 2023
$2.0M
Use of CRISPR/Cas9 to Treat Huntington DiseaseR33NS106120 · NINDS · EMORY UNIVERSITY · PI YAO, BING · 2021 to 2022
$778k
Using Human iPSC Models to Determine the Mechanism of Inflammation-Induced Disruption of Dopamine NeurotransmissionR21MH132012 · NIMH · EMORY UNIVERSITY · PI MILLER, ANDREW H, WEN, ZHEXING · 2022 to 2023
$430k
NIA NIH HHS R01 AG062577NIA NIH HHS R01 AG064786NIA NIH HHS R01 AG065611NIA NIH HHS R01 AG078937NIMH NIH HHS R01 MH117122NIMH NIH HHS R21 MH132012NINDS NIH HHS R01 NS110110NINDS NIH HHS R01 NS118819NINDS NIH HHS R33 NS106120U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) R01MH117122U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) R21MH132012U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01NS110110U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R01NS118819U.S. Department of Health & Human Services | NIH | National Institute of Neurological Disorders and Stroke (NINDS) R33NS106120U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) R01AG062577U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) R01AG064786U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) R01AG065611U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) R01AG078937
6 · The paper itself

Abstract

MicroRNAs (miRNAs) and long non-coding RNAs (lncRNAs) regulate broad gene networks through distinct mechanisms, which govern normal brain development and function but are dysregulated in schizophrenia (SCZ). However, how disease-risk miRNAs and lncRNAs co-operate to form pathogenic pathways in SCZ brains remain poorly understood. In this study, we identified a novel miRNA-lncRNA pathway in which the well-recognized SCZ-risk factor miR-137 enhances expression of the SCZ-risk lncRNA GOMAFU in human neuron development. We found significant up-regulation of GOMAFU during differentiation of multiple types of human neurons in vivo and in culture. Interestingly, the accumulation of histone acetylation, which activates numerous neuronal genes, down-regulates GOMAFU in iPSC-derived human neurons through inducing transcription repressors of GOMAFU, represented by the miR-137-target E2F6. We further demonstrated that miR-137 is necessary and sufficient for enhancing GOMAFU expression in a human neuronal progenitor cell (NPC) line and observed co-regulation of MIR137 with GOMAFU during normal human neuronal development and in SCZ brains. Moreover, we identified human NPC transcriptomic changes induced by miR-137 and discovered that miR-137 integrates functional co-operation of histone acetylation and transcription factors to promote GOMAFU expression. Notably, a significant number of miR-137-regulated transcription factors are predicted to bind the GOMAFU promoter and affected in SCZ brains, forming a highly interactive molecular network. Together, these results unveil the SCZ risk miR-137-GOMAFU non-coding RNA pathway connected by SCZ-affected transcription factors, providing a new mode of functional integration of non-coding and coding risk genes of SCZ that contributes to the complex etiology.

Indexed as

Gene Regulatory NetworksMicroRNAsRNA, Long NoncodingSchizophreniaBrainHumansInduced Pluripotent Stem CellsNeural Stem CellsNeuronsMicroRNAsMIRN137 microRNA, humanRNA, Long Noncoding

Identifiers

PMID41253765
PMCPMC12627607

What Socratic holds

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LicenceCC BY-NC-ND
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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 Socratic graph.