Evidence map›Paper›PMID 35984881›Full record

ArticleScience advances2022

Loss of schizophrenia-related miR-501-3p in mice impairs sociability and memory by enhancing mGluR5-mediated glutamatergic transmission.

Wenquan Liang, Yu Hou, Weiyuan Huang, Yunqian Wang, Tingyun Jiang, Xingbing Huang, Zhongju Wang, Fengchun Wu, Jiawei Zheng, Jie Zhang and 13 more

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.9field-weighted citation impact, top 7% 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

19 citing papers in PubMed, 34 citations in OpenAlex.

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  18. Role of MicroRNA-502-3p in Human Diseases.Pharmaceuticals (Basel, Switzerland) · 2023
    Review
  19. MicroRNA 3' ends shorten during adolescent brain maturation.Frontiers in molecular neuroscience · 2023
    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

23 authors at 6 institutions in 1 country.

Wenquan LiangDepartment of Medical Genetics, School of Basic Medical Sciences, and Guangdong Technology and Engineering Research Center for Molecular Diagnostics of Human Genetic Diseases, Southern Medical University, Guangzhou, Guangdong, China.ORCID 0000-0003-4645-4094
Yu HouDepartment of Medical Genetics, School of Basic Medical Sciences, and Guangdong Technology and Engineering Research Center for Molecular Diagnostics of Human Genetic Diseases, Southern Medical University, Guangzhou, Guangdong, China.ORCID 0000-0002-0799-391X
Weiyuan HuangDepartment of Neurobiology, School of Basic Medical Sciences, Southern Medical University, China.ORCID 0000-0002-8062-0255
Yunqian WangDepartment of Medical Genetics, School of Basic Medical Sciences, and Guangdong Technology and Engineering Research Center for Molecular Diagnostics of Human Genetic Diseases, Southern Medical University, Guangzhou, Guangdong, China.
Tingyun JiangThe Third People's Hospital of Zhongshan, Zhongshan, Guangdong, China.
Xingbing HuangDepartment of Psychiatry, The Affiliated Brain Hospital of Guangzhou Medical University (Guangzhou Huiai Hospital), Guangzhou, China.ORCID 0000-0002-2960-2502
Zhongju WangDepartment of Medical Genetics, School of Basic Medical Sciences, and Guangdong Technology and Engineering Research Center for Molecular Diagnostics of Human Genetic Diseases, Southern Medical University, Guangzhou, Guangdong, China.
Fengchun WuDepartment of Psychiatry, The Affiliated Brain Hospital of Guangzhou Medical University (Guangzhou Huiai Hospital), Guangzhou, China.ORCID 0000-0003-2817-2341
Jiawei ZhengDepartment of Neurobiology, School of Basic Medical Sciences, Southern Medical University, China.
Jie ZhangThe Third People's Hospital of Zhongshan, Zhongshan, Guangdong, China.ORCID 0000-0002-6025-4227
Haiyan OuDepartment of Medical Genetics, School of Basic Medical Sciences, and Guangdong Technology and Engineering Research Center for Molecular Diagnostics of Human Genetic Diseases, Southern Medical University, Guangzhou, Guangdong, China.
Shuyun LiDepartment of Psychiatry, The Affiliated Brain Hospital of Guangzhou Medical University (Guangzhou Huiai Hospital), Guangzhou, China.
Junjiao PingThe Third People's Hospital of Zhongshan, Zhongshan, Guangdong, China.
Yuan ZhangDepartment of Neurobiology, School of Basic Medical Sciences, Southern Medical University, China.
Junping YeDepartment of Medical Genetics, School of Basic Medical Sciences, and Guangdong Technology and Engineering Research Center for Molecular Diagnostics of Human Genetic Diseases, Southern Medical University, Guangzhou, Guangdong, China.
Zhongwei LiDepartment of Medical Genetics, School of Basic Medical Sciences, and Guangdong Technology and Engineering Research Center for Molecular Diagnostics of Human Genetic Diseases, Southern Medical University, Guangzhou, Guangdong, China.ORCID 0000-0001-8924-3145
Qiong YangDepartment of Psychiatry, The Affiliated Brain Hospital of Guangzhou Medical University (Guangzhou Huiai Hospital), Guangzhou, China.
Jian ZhangDepartment of Medical Genetics, School of Basic Medical Sciences, and Guangdong Technology and Engineering Research Center for Molecular Diagnostics of Human Genetic Diseases, Southern Medical University, Guangzhou, Guangdong, China.ORCID 0000-0002-0790-4462
Xianzhen ZhengGuangdong General Hospital, Guangdong Academy of Medical Science and Guangdong Mental Health Center, Guangzhou, China.
Shufen LiDepartment of Medical Genetics, School of Basic Medical Sciences, and Guangdong Technology and Engineering Research Center for Molecular Diagnostics of Human Genetic Diseases, Southern Medical University, Guangzhou, Guangdong, China.
Xin-Hong ZhuDepartment of Neurobiology, School of Basic Medical Sciences, Southern Medical University, China.
Rongqing ChenDepartment of Neurobiology, School of Basic Medical Sciences, Southern Medical University, China.ORCID 0000-0002-1668-8554
Cunyou ZhaoDepartment of Medical Genetics, School of Basic Medical Sciences, and Guangdong Technology and Engineering Research Center for Molecular Diagnostics of Human Genetic Diseases, Southern Medical University, Guangzhou, Guangdong, China.ORCID 0000-0001-6116-4584
Southern Medical University · CNZhongshan People's Hospital · CNGuangzhou Medical University · CNZhujiang Hospital · CNChinese PLA General Hospital · CNGuangdong General Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Schizophrenia is a polygenetic disease, the heterogeneity of which is likely complicated by epigenetic modifications yet to be elucidated. Here, we performed transcriptomic analysis of peripheral blood RNA from monozygotic twins discordant for schizophrenia and identified a schizophrenia-associated down-regulated microRNA, miR-501-3p. We showed that the loss of miR-501-3p in germline knockout (KO) male mice resulted in dendritic structure defects, glutamatergic transmission enhancement, and sociability, memory, and sensorimotor gating disruptions, which were attenuated when miR-501 expression was conditionally restored in the nervous system. Combining the results of proteomic analyses with the known genes linked to schizophrenia revealed that metabotropic glutamate receptor 5 (mGluR5) was one of the miR-501-3p targets and was elevated in vivo upon loss of miR-501. Treatment with the mGluR5 negative allosteric modulator 3-2((-methyl-4-thiazolyl) ethynyl) pyridine or the

Indexed as

MicroRNAsReceptor, Metabotropic Glutamate 5SchizophreniaAnimalsMaleMiceMice, KnockoutProteomicsMicroRNAsMIRN501 microRNA, mouseReceptor, Metabotropic Glutamate 5

Identifiers

PMID35984881
PMCPMC9390987
OpenAlexW4292386818

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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.