乌朱沁羊肌内脂肪沉积相关lncRNA和miRNA ceRNA网络的构建

IF 2.6 2区 农林科学 Q1 VETERINARY SCIENCES
Frontiers in Veterinary Science Pub Date : 2025-03-19 eCollection Date: 2025-01-01 DOI:10.3389/fvets.2025.1559727
Mingxi Lan, Qing Qin, Yuchun Xie, Chongyan Zhang, Zhichen Liu, Xiaolong Xu, Jingwen Zhang, Songsong Xu, Ji Yang, Haijun Zhang, Suhe Alatan, Zhixin Wang, Zhihong Liu
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引用次数: 0

摘要

摘要:肌内脂肪(IMF)沉积的分子机制对提高羊肉品质至关重要。这一过程受转录因子网络的调控。探索非编码rna,特别是lncRNAs和miRNAs在IMF沉积中的作用,可以阐明其复杂的遗传学,为内蒙古地方品种的育种提供资源。方法选用60只体重相近的6月龄乌朱沁羊,对胴体和羊肉品质参数进行评价。为了研究非编码RNA在IMF沉积中的作用,我们鉴定了背最长肌和股二头肌之间差异表达的基因和途径。此外,我们分析了这些基因和lncRNA-miRNA-mRNA在高和低imf股二头肌组中的共调控网络。结果:我们鉴定出11529种mrna(747种差异表达),9874种lncrna(1428种差异表达)和761种mirna(12种差异表达)。GO和KEGG富集分析表明,这些基因参与脂质代谢、脂肪酸氧化和能量代谢。我们构建了一个包含12个lncrna、4个mirna和6个mrna的ceRNA网络。值得注意的是,lncRNA MSTRG.13155.1与miR-1343-3p_R + 2相互作用,通过释放HADHA基因表达促进IMF沉积。双荧光素酶报告基因检测证实MSTRG.13155.1和HADHA是miR-1343-3p_R + 2的靶标。RT-qPCR验证了关键mrna、mirna和lncrna的表达趋势,与测序结果一致。讨论:我们综合分析了乌朱姆沁羊背最长肌和股二头肌以及高、低IMF组的差异表达基因和途径,揭示了IMF沉积的复杂遗传学。这为内蒙古地方品种选择提供了宝贵的资源。lncRNA MSTRG.13155.1与miR-1343-3p_R + 2的相互作用及其对HADHA表达的调控,为研究IMF沉积机制提供了新的思路。未来的研究可以探索这些机制在不同品种和环境中的普遍性和特异性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Construction of ceRNA networks of lncRNA and miRNA associated with intramuscular fat deposition in Ujumqin sheep.

Introduction: The molecular mechanisms underlying intramuscular fat (IMF) deposition are crucial for enhancing lamb meat quality. This process is regulated by a network of transcription factors. Exploring the role of non-coding RNAs, particularly lncRNAs and miRNAs, in IMF deposition can clarify its complex genetics and offer resources for breeding Inner Mongolian local breeds.

Methods: We evaluated carcass and lamb meat quality parameters using 60 six-month-old Ujumqin sheep with similar body weights. To investigate non-coding RNA's role in IMF deposition, we identified differentially expressed genes and pathways between the longissimus dorsi and femoral biceps. Additionally, we analyzed these genes and the lncRNA-miRNA-mRNA co-regulatory network in high- and low-IMF femoral biceps groups.

Results: We identified 11,529 mRNAs (747 differentially expressed), 9,874 lncRNAs (1,428 differentially expressed), and 761 miRNAs (12 differentially expressed). GO and KEGG enrichment analyses showed these genes are involved in lipid metabolism, fatty acid oxidation, and energy metabolism. We constructed a ceRNA network with 12 lncRNAs, 4 miRNAs, and 6 mRNAs. Notably, lncRNA MSTRG.13155.1 interacts with miR-1343-3p_R + 2, promoting IMF deposition by releasing HADHA gene expression. Dual-luciferase reporter assays confirmed MSTRG.13155.1 and HADHA as miR-1343-3p_R + 2 targets. RT-qPCR validated the expression trends of key mRNAs, miRNAs, and lncRNAs, consistent with sequencing results.

Discussion: Our comprehensive analysis of differentially expressed genes and pathways in Ujumqin sheep's longissimus dorsi and femoral biceps, along with high- and low-IMF groups, has revealed the complex genetics of IMF deposition. This offers valuable resources for Inner Mongolian local breed selection. The interaction between lncRNA MSTRG.13155.1 and miR-1343-3p_R + 2, and their regulation of HADHA expression, provides new insights into IMF deposition mechanisms. Future research can explore these mechanisms' universality and specificity across different breeds and environments.

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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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