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微小RNA在牛卵母细胞成熟及生殖调控中的作用

Role of miRNAs in Bovine Oocyte Maturation and Reproductive Regulation.

作者信息

Yang Xiaogeng, He Honghong, Wang Peng, Wang Yaying, Wang Linlin, Yang Falong, Li Jian, Zhang Huizhu

机构信息

Key Laboratory of Animal Medicine, Southwest Minzu University of Sichuan Province, Chengdu 610041, China.

Key Laboratory of Qinghai-Tibetan Plateau Animal Genetic Resource Reservation and Utilization, Ministry of Education, Chengdu 610041, China.

出版信息

Int J Mol Sci. 2025 Mar 21;26(7):2828. doi: 10.3390/ijms26072828.

DOI:10.3390/ijms26072828
PMID:40243418
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11989158/
Abstract

MicroRNAs (miRNAs) are a class of endogenous small non-coding RNAs that regulate target gene expression in many eukaryotes. MiRNAs are essential for post-transcriptional regulation, influencing various biological functions, including oocyte growth and maturation, fertilization, early embryo development, and implantation. In recent decades, numerous studies have identified a substantial number of miRNAs associated with mammalian oocyte maturation and early embryo development, utilizing methods such as small RNA sequencing and modulating miRNA expression through overexpression or inhibition. In this review, we introduce the biosynthesis of miRNAs and their regulatory roles in germ cells, summarizing the expression patterns and post-transcriptional regulation of miRNAs during oocyte maturation and early embryo development, as well as their potential application in assisted reproductive technology (ART).

摘要

微小RNA(miRNA)是一类内源性小非编码RNA,可在许多真核生物中调节靶基因表达。miRNA对于转录后调控至关重要,影响多种生物学功能,包括卵母细胞生长和成熟、受精、早期胚胎发育和着床。近几十年来,众多研究利用小RNA测序等方法,并通过过表达或抑制来调节miRNA表达,已鉴定出大量与哺乳动物卵母细胞成熟和早期胚胎发育相关的miRNA。在本综述中,我们介绍了miRNA的生物合成及其在生殖细胞中的调控作用,总结了miRNA在卵母细胞成熟和早期胚胎发育过程中的表达模式和转录后调控,以及它们在辅助生殖技术(ART)中的潜在应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ac7/11989158/bf3c8f0658f0/ijms-26-02828-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ac7/11989158/3e88abde16a9/ijms-26-02828-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ac7/11989158/bf3c8f0658f0/ijms-26-02828-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ac7/11989158/3e88abde16a9/ijms-26-02828-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8ac7/11989158/bf3c8f0658f0/ijms-26-02828-g002.jpg

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本文引用的文献

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Bta-miR-665 improves bovine blastocyst development through its influence on microtubule dynamics and apoptosis.Bta- miR-665通过影响微管动力学和细胞凋亡来改善牛囊胚发育。
Front Genet. 2024 Oct 16;15:1437695. doi: 10.3389/fgene.2024.1437695. eCollection 2024.
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From follicle to blastocyst: microRNA-34c from follicular fluid-derived extracellular vesicles modulates blastocyst quality.从卵泡到囊胚:卵泡液来源的细胞外囊泡中的微小RNA-34c调节囊胚质量。
J Anim Sci Biotechnol. 2024 Aug 4;15(1):104. doi: 10.1186/s40104-024-01059-8.
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Expression profile and gap-junctional transfer of microRNAs in the bovine cumulus-oocyte complex.
牛卵丘-卵母细胞复合体中微小RNA的表达谱及间隙连接转运
Front Cell Dev Biol. 2024 Jul 11;12:1404675. doi: 10.3389/fcell.2024.1404675. eCollection 2024.
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Follicular fluid HD-sevs-mir-128-3p is a key molecule in regulating bovine granulosa cells autophagy.卵泡液 HD-sevs-mir-128-3p 是调控牛颗粒细胞自噬的关键分子。
Theriogenology. 2024 Sep 15;226:263-276. doi: 10.1016/j.theriogenology.2024.06.022. Epub 2024 Jun 28.
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Role of miRNAs in assisted reproductive technology.miRNAs 在辅助生殖技术中的作用。
Gene. 2024 Nov 15;927:148703. doi: 10.1016/j.gene.2024.148703. Epub 2024 Jun 15.
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MicroRNA-148b secreted by bovine oviductal extracellular vesicles enhance embryo quality through BPM/TGF-beta pathway.牛输卵管腔外小泡分泌的 microRNA-148b 通过 BPM/TGF-beta 通路增强胚胎质量。
Biol Res. 2024 Mar 23;57(1):11. doi: 10.1186/s40659-024-00488-z.
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MicroRNAs in spermatogenesis dysfunction and male infertility: clinical phenotypes, mechanisms and potential diagnostic biomarkers.微小 RNA 在精子发生功能障碍和男性不育症中的作用:临床表型、机制和潜在的诊断生物标志物。
Front Endocrinol (Lausanne). 2024 Feb 16;15:1293368. doi: 10.3389/fendo.2024.1293368. eCollection 2024.
8
Bta-miR-301a targets ACVR1 to influence cleavage time and blastocyst formation rate of early embryos in cattle.牛Bta-miR-301a靶向激活素受体1(ACVR1)以影响牛早期胚胎的卵裂时间和囊胚形成率。
Biol Reprod. 2024 Feb 6. doi: 10.1093/biolre/ioae024.
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