Evidence map›Paper›PMID 27221778›Full record

ArticleScientific reports2016

miR-9 and miR-124 synergistically affect regulation of dendritic branching via the AKT/GSK3β pathway by targeting Rap2a.

Qian Xue, Caiyong Yu, Yan Wang, Ling Liu, Kun Zhang, Chao Fang, Fangfang Liu, Ganlan Bian, Bing Song, Angang Yang and 2 more

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 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

49 citing papers in PubMed, 76 citations in OpenAlex.

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  15. Review
  16. Neuronal microRNAs safeguard ER CaCellular and molecular life sciences : CMLS · 2022
    Article
  17. Article
  18. Article
  19. Review
  20. 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

12 authors at 3 institutions in 2 countries.

Qian XueInstitute of Neurosciences, the Fourth Military Medical University, Xi'an 710032, China.
Caiyong YuInstitute of Neurosciences, the Fourth Military Medical University, Xi'an 710032, China.
Yan WangOral and maxillofacial surgery, Stomatology Hospital of Xi'an Jiaotong University, 710004, China.
Ling LiuInstitute of Neurosciences, the Fourth Military Medical University, Xi'an 710032, China.
Kun ZhangInstitute of Neurosciences, the Fourth Military Medical University, Xi'an 710032, China.
Chao FangInstitute of Neurosciences, the Fourth Military Medical University, Xi'an 710032, China.
Fangfang LiuInstitute of Neurosciences, the Fourth Military Medical University, Xi'an 710032, China.
Ganlan BianInstitute of Neurosciences, the Fourth Military Medical University, Xi'an 710032, China.
Bing SongCardiff Institute of Tissue Engineering &Repair, School of Dentistry, Cardiff University, Cardiff, CF14 4XY, UK.
Angang YangDepartment of Immunology, the Fourth Military Medical University, Xi'an 710032, China.
Gong JuInstitute of Neurosciences, the Fourth Military Medical University, Xi'an 710032, China.
Jian WangInstitute of Neurosciences, the Fourth Military Medical University, Xi'an 710032, China.
Air Force Medical University · CNCardiff University · GBXi'an Jiaotong University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A single microRNA (miRNA) can regulate expression of multiple proteins, and expression of an individual protein may be controlled by numerous miRNAs. This regulatory pattern strongly suggests that synergistic effects of miRNAs play critical roles in regulating biological processes. miR-9 and miR-124, two of the most abundant miRNAs in the mammalian nervous system, have important functions in neuronal development. In this study, we identified the small GTP-binding protein Rap2a as a common target of both miR-9 and miR-124. miR-9 and miR-124 together, but neither miRNA alone, strongly suppressed Rap2a, thereby promoting neuronal differentiation of neural stem cells (NSCs) and dendritic branching of differentiated neurons. Rap2a also diminished the dendritic complexity of mature neurons by decreasing the levels of pAKT and pGSK3β. Our results reveal a novel pathway in which miR-9 and miR-124 synergistically repress expression of Rap2a to sustain homeostatic dendritic complexity during neuronal development and maturation.

Indexed as

3' Untranslated RegionsAnimalsDendritesGene Expression RegulationGlycogen Synthase Kinase 3 betaHEK293 CellsHomeostasisHumansMiceMicroRNAsNeural Stem CellsNeurogenesisNeuronsProto-Oncogene Proteins c-aktrap GTP-Binding ProteinsRecombinant Fusion Proteins3' Untranslated RegionsGlycogen Synthase Kinase 3 betaMicroRNAsMirn124 microRNA, mouseMIRN9 microRNA, mouseProto-Oncogene Proteins c-aktRap2a protein, mouserap GTP-Binding ProteinsRecombinant Fusion Proteins

Identifiers

PMID27221778
PMCPMC4879704
OpenAlexW2406809367

What OpenQuestion holds

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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.