Evidence map›Paper›PMID 39702498›Full record

ArticleCommunications biology2024

A miR-219-5p-bmal1b negative feedback loop contributes to circadian regulation in zebrafish.

Lianxin Wu, Meng Zhao, Xifeng Chen, Han Wang

Abstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

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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

4 citing papers in PubMed.

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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

4 authors.

Lianxin Wu *Center for Circadian Clocks, Soochow University, Suzhou, Jiangsu, China.
Meng Zhao *Center for Circadian Clocks, Soochow University, Suzhou, Jiangsu, China.
Xifeng Chen *Center for Circadian Clocks, Soochow University, Suzhou, Jiangsu, China.
Han WangCenter for Circadian Clocks, Soochow University, Suzhou, Jiangsu, China. han.wang88@gmail.com.ORCID 0000-0003-2420-3147

Funding

National Natural Science Foundation of China (National Science Foundation of China) 31961133026National Natural Science Foundation of China (National Science Foundation of China) 81570171National Natural Science Foundation of China (National Science Foundation of China) 81701347
6 · The paper itself

Abstract

MicroRNAs post-transcriptionally regulate gene expression and contribute to numerous life processes, including circadian rhythms. However, whether miRNAs contribute to zebrafish circadian regulation has not yet been investigated. Here, we showed that mature miR-219-5p, and its three pre-miRNAs, mir-219-1, mir-219-2, and mir-219-3, are rhythmically expressed primarily in Tectum opticum (TeO), Corpus cerebelli (CCe), and Crista cerellaris (CC) of the zebrafish brain. While mir-219-1 and mir-219-2 are regulated by the circadian clock through the E-like box, mir-219-3 is regulated by light via the D-box. Deleting mir-219-1, mir-219-2, or mir-219-3 individually or knocking down miR-219-5p all results in a shortened period of locomotor rhythms and up-regulation of bmal1b. RIP assays with Ago2 and miRNA pull-down assays show that miR-219-5p binds to bmal1b in the RISC. Cell transfection and in Vivo assays show that miR219-5p inhibits bmal1b through binding to its 3'UTR. Further, transcriptome analysis of miR-219-5p knockdown zebrafish adult brain reveals possible roles of miR-219-5p in phototransduction and neuroactive ligand-receptor interaction. Together, our findings demonstrate that mir-219-1, mir-219-2, and mir-219-3 are controlled directly by the circadian clock; and in turn, miR-219-5p contributes to circadian regulation by targeting bmal1b, highlighting a miR-219-5p-bmal1b negative feedback loop in the zebrafish circadian circuit.

Indexed as

Circadian RhythmMicroRNAsZebrafishZebrafish ProteinsAnimalsARNTL Transcription FactorsFeedback, PhysiologicalGene Expression RegulationARNTL Transcription FactorsMicroRNAsZebrafish Proteins

Identifiers

PMID39702498
PMCPMC11659407

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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.