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一个miR-219-5p-bmal1b负反馈环有助于斑马鱼的昼夜节律调节。

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

作者信息

Wu Lianxin, Zhao Meng, Chen Xifeng, Wang Han

机构信息

Center for Circadian Clocks, Soochow University, Suzhou, Jiangsu, China.

School of Basic Medical Sciences, Suzhou Medical College, Soochow University, Suzhou, Jiangsu, China.

出版信息

Commun Biol. 2024 Dec 19;7(1):1671. doi: 10.1038/s42003-024-07309-9.

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.

摘要

微小RNA在转录后水平调控基因表达,并参与包括昼夜节律在内的众多生命过程。然而,微小RNA是否参与斑马鱼的昼夜节律调控尚未得到研究。在此,我们发现成熟的miR-219-5p及其三个前体微小RNA,即mir-219-1、mir-219-2和mir-219-3,主要在斑马鱼大脑的视顶盖(TeO)、小脑体(CCe)和小脑嵴(CC)中有节律地表达。虽然mir-219-1和mir-219-2通过E样框受昼夜节律钟调控,但mir-219-3通过D框受光调控。单独删除mir-219-1、mir-219-2或mir-219-3,或敲低miR-219-5p,均会导致运动节律周期缩短以及bmal1b上调。用Ago2进行的RNA免疫沉淀分析(RIP分析)和微小RNA下拉分析表明,miR-219-5p在RNA诱导沉默复合体(RISC)中与bmal1b结合。细胞转染和体内实验表明,miR219-5p通过与其3'非翻译区(3'UTR)结合来抑制bmal1b。此外,对miR-219-5p敲低的斑马鱼成体大脑进行转录组分析,揭示了miR-219-5p在光转导和神经活性配体-受体相互作用中的可能作用。总之,我们的研究结果表明,mir-219-1、mir-219-2和mir-219-3直接受昼夜节律钟控制;反过来,miR-219-5p通过靶向bmal1b参与昼夜节律调控,突出了斑马鱼昼夜节律回路中的miR-219-5p-bmal1b负反馈环。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66b8/11659407/8d8128b44ad4/42003_2024_7309_Fig1_HTML.jpg

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