Lnc MSTRG 4701.7 targets miR-1786/RORa to competitively regulate proliferation and apoptosis in chicken follicular granulosa cells.

IF 2.6 2区 农林科学 Q1 VETERINARY SCIENCES
Frontiers in Veterinary Science Pub Date : 2025-04-30 eCollection Date: 2025-01-01 DOI:10.3389/fvets.2025.1583287
Chang Ma, Hengsong Wu, Chunchi Yan, Simushi Liswaniso, Xue Sun, Ning Qin, Rifu Xu
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引用次数: 0

Abstract

Background: Follicular development in chickens is a highly coordinated and complex process. While the hypothalamic-pituitary-gonadal axis plays a central regulatory role in this process, the role of long noncoding RNAs (LncRNAs) remains unclear. Here, we aimed to identify key differentially expressed LncRNAs and explore their regulatory roles in follicular development, particularly focusing on the MSTRG.4701.7-miR-1786-RORa axis, to provide insights for improving fertility in low-fertility chicken varieties.

Methods: Intact follicular tissues were collected from Jilin Black chickens (low-fertility group) and Lohmann Brown Laying hens (high-fertility group) at each stage of ovarian development for transcriptome sequencing to identify key differentially expressed LncRNAs for follow-up analyses. Bioinformatics analysis was also performed to determine the role of the MSTRG.4701.7-miR-1786-RORa regulatory axis, and to clarify whether that MSTRG 4701.7 targets miR-1786/RORa to competitively regulate the proliferation and differentiation of chicken follicular granulosa cells (GCs). We also knocked down and overexpressed key genes, MSTRG.4701.7 and miR-1786 and thereafter, determined changes in the mRNA and protein expression levels of axial terminal mRNA-RORa.

Results: MSTRG.4701.7 promotes the apoptosis of chicken follicular GCs, while miR-1786 reverses this phenomenon. RORa was also identified as a functional target of miR-1786 in GCs, and as a competitive endogenous RNA, MSTRG.4701.7 regulated RORa expression by sponging miR-1786, thereby playing a regulatory role in GCs. Additionally, interfering with MSTRG.4701.7 expression significantly downregulated RORa mRNA and protein expression levels, while interfering with miR-1786 showed the opposite effect.

Conclusion: MSTRG.4701.7 plays a critical role in follicular development in chickens by influencing GC proliferation, differentiation, and apoptosis. The resent results provide useful molecular evidence for elucidating the genetic mechanism underlying ovarian follicle development associated with egg production in chicken.

Lnc MSTRG 4701.7靶向miR-1786/RORa竞争性调节鸡滤泡颗粒细胞的增殖和凋亡。
背景:鸡卵泡发育是一个高度协调和复杂的过程。虽然下丘脑-垂体-性腺轴在这一过程中起着中心调节作用,但长链非编码rna (LncRNAs)的作用尚不清楚。在这里,我们旨在确定关键的差异表达lncrna,并探索其在卵泡发育中的调节作用,特别是关注MSTRG.4701.7-miR-1786-RORa轴,为提高低育性鸡品种的育性提供见解。方法:采集吉林黑鸡(低生育能力组)和罗曼布朗蛋鸡(高生育能力组)卵巢发育各阶段的完整卵泡组织,进行转录组测序,鉴定关键差异表达lncrna,用于后续分析。我们还进行了生物信息学分析,以确定MSTRG.4701.7-miR-1786-RORa调控轴的作用,并阐明MSTRG 4701.7是否靶向miR-1786/RORa竞争性地调控鸡滤泡颗粒细胞(GCs)的增殖和分化。我们还敲除和过表达关键基因MSTRG.4701.7和miR-1786,然后测定轴端mRNA- rora mRNA和蛋白表达水平的变化。结果:MSTRG.4701.7促进了鸡卵泡GCs的凋亡,而miR-1786逆转了这一现象。RORa也是miR-1786在GCs中的功能靶点,MSTRG.4701.7作为一种竞争性内源性RNA,通过海绵化miR-1786调控RORa的表达,从而在GCs中发挥调控作用。此外,干扰MSTRG.4701.7表达可显著下调RORa mRNA和蛋白表达水平,而干扰miR-1786则相反。结论:MSTRG.4701.7通过影响GC增殖、分化和凋亡在鸡卵泡发育中起关键作用。这些结果为阐明鸡卵泡发育与产蛋相关的遗传机制提供了有用的分子证据。
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来源期刊
Frontiers in Veterinary Science
Frontiers in Veterinary Science Veterinary-General Veterinary
CiteScore
4.80
自引率
9.40%
发文量
1870
审稿时长
14 weeks
期刊介绍: Frontiers in Veterinary Science is a global, peer-reviewed, Open Access journal that bridges animal and human health, brings a comparative approach to medical and surgical challenges, and advances innovative biotechnology and therapy. Veterinary research today is interdisciplinary, collaborative, and socially relevant, transforming how we understand and investigate animal health and disease. Fundamental research in emerging infectious diseases, predictive genomics, stem cell therapy, and translational modelling is grounded within the integrative social context of public and environmental health, wildlife conservation, novel biomarkers, societal well-being, and cutting-edge clinical practice and specialization. Frontiers in Veterinary Science brings a 21st-century approach—networked, collaborative, and Open Access—to communicate this progress and innovation to both the specialist and to the wider audience of readers in the field. Frontiers in Veterinary Science publishes articles on outstanding discoveries across a wide spectrum of translational, foundational, and clinical research. The journal''s mission is to bring all relevant veterinary sciences together on a single platform with the goal of improving animal and human health.
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