Evidence map›Paper›PMID 27716060›Full record

ArticleBMC genomics2016

miR-27b shapes the presynaptic transcriptome and influences neurotransmission by silencing the polycomb group protein Bmi1.

Vivian Y Poon, Minxia Gu, Fang Ji, Antonius M VanDongen, Marc Fivaz

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.0field-weighted citation impact, top 24% 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

15 citing papers in PubMed, 28 citations in OpenAlex.

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  12. Epigenetics of the Synapse in Neurodegeneration.Current neurology and neuroscience reports · 2019
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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

5 authors at 2 institutions in 1 country.

Vivian Y PoonProgram in Neuroscience and Behavioral Disorders, Duke-NUS Medical School, Singapore, Singapore.
Minxia GuProgram in Neuroscience and Behavioral Disorders, Duke-NUS Medical School, Singapore, Singapore.
Fang JiProgram in Neuroscience and Behavioral Disorders, Duke-NUS Medical School, Singapore, Singapore.
Antonius M VanDongenProgram in Neuroscience and Behavioral Disorders, Duke-NUS Medical School, Singapore, Singapore.
Marc FivazProgram in Neuroscience and Behavioral Disorders, Duke-NUS Medical School, Singapore, Singapore. marc.fivaz@duke-nus.edu.sg.ORCID 0000-0003-1003-7934
Duke-NUS Medical School · SGNational University of Singapore · SG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicroRNAs (miRNAs) are short non-coding RNAs that are emerging as important post-transcriptional regulators of neuronal and synaptic development. The precise impact of miRNAs on presynaptic function and neurotransmission remains, however, poorly understood.

resultsHere, we identify miR-27b-an abundant neuronal miRNA implicated in neurological disorders-as a global regulator of the presynaptic transcriptome. miR-27b influences the expression of three quarters of genes associated with presynaptic function in cortical neurons. Contrary to expectation, a large majority of these genes are up-regulated by miR-27b. This stimulatory effect is mediated by miR-27b-directed silencing of several transcriptional repressors that cooperate to suppress the presynaptic transcriptome. The strongest repressive activity appears to be mediated by Bmi1, a component of the polycomb repressive complex implicated in self-renewal of neural stem cells. miR-27b knockdown leads to reduced synaptogenesis and to a marked decrease in neural network activity, which is fully restored by RNAi-mediated silencing of Bmi1.

conclusionsWe conclude that silencing of Bmi1 by miR-27b relieves repression of the presynaptic transcriptome and supports neurotransmission in cortical networks. These results expand the repressive activity of Bmi1 to genes involved in synaptic function and identify a unique post-transcriptional circuitry that stimulates expression of synaptic genes and promotes synapse differentiation.

Indexed as

Gene SilencingTranscriptomeAnimalsCluster AnalysisGene Expression ProfilingGene Expression Regulation, NeoplasticMiceMicroRNAsNeural PathwaysPolycomb Repressive Complex 1Presynaptic TerminalsProto-Oncogene ProteinsRatsRepressor ProteinsRNA InterferenceRNA, MessengerBmi1 protein, mouseMicroRNAsMirn27 microRNA, mousePolycomb Repressive Complex 1Proto-Oncogene ProteinsRepressor ProteinsRNA, MessengerSox11 protein, mouseSOXC Transcription FactorsZfp90 protein, mouseEpigeneticsmiRNAsNeurotransmissionPolycomb Group ProteinSynapseTranscriptome

Identifiers

PMID27716060
PMCPMC5050705
OpenAlexW2527907880

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.