Preliminary construction of non-coding RNAs and ceRNA regulatory networks mediated by exosomes in porcine follicular fluid

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Yangguang Liu , Fan Xie , Huibin Zhang , Haibo Ye , Haoyu Wen , Mengyao Qiu , Yueyun Ding , Xianrui Zheng , Zongjun Yin , Xiaodong Zhang
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引用次数: 0

Abstract

Background

Follicles are fundamental units of the ovary, regulated intricately during development. Exosomes and ovarian granulosa cells (OGCs) play pivotal roles in follicular development, yet the regulatory mechanisms governing exosomes remain elusive.

Results

High-throughput sequencing was employed to evaluate the complete transcript expression profiles of six samples (three porcine ovarian granulosa cells-exosome co-culture samples (GCE) and three porcine ovarian granulosa cells (POGCs) samples). Differential expression analysis revealed 924 lncRNAs, 35 circRNAs, 49 miRNAs, and 9823 mRNAs in the GCE group. Gene ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analyses indicated enrichment of differentially expressed transcripts in pathways related to cell proliferation and apoptosis. Furthermore, a ceRNA regulatory network comprising 43 lncRNAs, 6 circRNAs, 11 miRNAs, and 126 mRNAs was constructed based on intergene co-expression correlations. Seven miRNAs associated with cell proliferation and apoptosis regulation were identified within this network, encompassing 92 subnet pairs as candidate genes for further exploration of exosome regulatory mechanisms. Additionally, preliminary verification at the cellular level demonstrated that exosomal miR-200b enhances the viability of POGCs.

Conclusions

Transcriptome analysis unveiled a pivotal candidate ceRNA network potentially implicated in exosome-mediated regulation of granulosa cell proliferation and apoptosis, thereby influencing porcine follicular development. These findings offer insights into the molecular mechanisms of follicular fluid exosome regulation, encompassing both coding and non-coding RNA perspectives.

初步构建猪卵泡液中由外泌体介导的非编码 RNA 和 ceRNA 调控网络。
背景:卵泡是卵巢的基本单位,在发育过程中受到复杂的调控。外泌体和卵巢颗粒细胞(OGCs)在卵泡发育过程中起着关键作用,但外泌体的调控机制仍然难以捉摸:采用高通量测序评估了六个样本(三个猪卵巢颗粒细胞-外泌体共培养样本(GCE)和三个猪卵巢颗粒细胞(POGCs)样本)的完整转录本表达谱。差异表达分析显示,GCE 组有 924 个 lncRNA、35 个 circRNA、49 个 miRNA 和 9823 个 mRNA。基因本体(GO)和京都基因组百科全书(KEGG)通路分析表明,差异表达的转录本富集在与细胞增殖和凋亡相关的通路中。此外,根据基因间共表达相关性,构建了一个由 43 个 lncRNA、6 个 circRNA、11 个 miRNA 和 126 个 mRNA 组成的 ceRNA 调控网络。在该网络中发现了 7 个与细胞增殖和凋亡调控相关的 miRNA,包括 92 个子网络对,作为进一步探索外泌体调控机制的候选基因。此外,细胞水平的初步验证表明,外泌体miR-200b能增强POGCs的活力:转录组分析揭示了一个关键的候选 ceRNA 网络,它可能与外泌体介导的颗粒细胞增殖和凋亡调控有关,从而影响猪的卵泡发育。这些发现从编码和非编码 RNA 两个角度揭示了卵泡液外泌体调控的分子机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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