与雄性繁殖力有关的萨希瓦尔牛精浆细胞外囊泡 (EV) 中微小核糖核酸的丰度差异。

IF 4.6 2区 生物学 Q2 CELL BIOLOGY
Frontiers in Cell and Developmental Biology Pub Date : 2024-10-01 eCollection Date: 2024-01-01 DOI:10.3389/fcell.2024.1473825
Vitika Chauhan, Poonam Kashyap, Jatinder Singh Chera, Ankit Pal, Aditya Patel, Seema Karanwal, Shiva Badrhan, Fanny Josan, Subhash Solanki, Mukesh Bhakat, Tirtha Kumar Datta, Rakesh Kumar
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引用次数: 0

摘要

萨希瓦尔牛以产奶量高而著称,通过人工授精(AI)利用雄性种质进行繁殖,主要取决于精液质量。精子产生于睾丸,携带着成功受精所必需的遗传信息和分子信号。精浆中除精子外,还含有纳米级的脂质结合细胞外囊泡(SP-EV),这些囊泡携带着关键的生物大分子,包括对公牛生育至关重要的与生育相关的 miRNA。目前的研究重点是对高繁殖力(HF)和低繁殖力(LF)萨希瓦尔公牛的SP-EVs进行miRNA分析。使用尺寸排阻色谱法(SEC)分离了SP-EV,并通过动态光散射(DLS)和纳米颗粒跟踪分析(NTA)对其进行了表征。免疫印迹检测到了EV特异性蛋白质标记物TSG101和CD63。DLS 分析显示,高频样品中的 SP-EV 尺寸为 170-180 nm,低频样品中的 SP-EV 尺寸为 130-140 nm。NTA显示高频组的颗粒浓度为5.76 × 1010至5.86 × 1011个/毫升,低频组为5.31 × 1010至2.70 × 1011个/毫升,高频组和低频组的颗粒大小和浓度无显著差异。高通量 miRNA 测序在两组 SP-EVs 中均发现了 310 个 miRNAs,其中高频公牛有 61 个上调,119 个下调。进一步分析发现了41个具有显著折叠变化和p值的miRNA,包括bta-miR-1246、bta-miR-195、bta-miR-339b和bta-miR-199b,并对其进行了靶基因预测分析。基因本体(GO)和 KEGG 通路分析表明,这些 miRNA 的靶基因涉及转录调控、泛素依赖性内质网相关降解(ERAD)通路和信号通路。qPCR 分析表明,bta-miR-195 在高频精子中的表达量比低频精子高 80%,这表明它与生育状况有关(p < 0.05)。总之,本研究阐明了作为萨希瓦尔公牛繁殖力指标的SP-EVs中的miRNA载体,并强调bta-miR-195是已鉴定的各种miRNA中的一个潜在繁殖力因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Differential abundance of microRNAs in seminal plasma extracellular vesicles (EVs) in Sahiwal cattle bull related to male fertility.

Sahiwal cattle, known for their high milk yield, are propagated through artificial insemination (AI) using male germplasm, largely contingent on semen quality. Spermatozoa, produced in the testes, carry genetic information and molecular signals essential for successful fertilization. Seminal plasma, in addition to sperm, contains nano-sized lipid-bound extracellular vesicles (SP-EVs) that carry key biomolecules, including fertility-related miRNAs, which are essential for bull fertility. The current study focused on miRNA profiling of SP-EVs from high-fertile (HF) and low-fertile (LF) Sahiwal bulls. SP-EVs were isolated using size exclusion chromatography (SEC) and characterized by dynamic light scattering (DLS) and nanoparticle tracking analysis (NTA). Western blotting detected the EV-specific protein markers TSG101 and CD63. The DLS analysis showed SP-EV sizes of 170-180 nm in HF and 130-140 nm in LF samples. The NTA revealed particle concentrations of 5.76 × 1010 to 5.86 × 1011 particles/mL in HF and 5.31 × 1010 to 2.70 × 1011 particles/mL in LF groups, with no significant differences in size and concentration between HF and LF. High-throughput miRNA sequencing identified 310 miRNAs in SP-EVs from both groups, with 61 upregulated and 119 downregulated in HF bull. Further analysis identified 41 miRNAs with significant fold changes and p-values, including bta-miR-1246, bta-miR-195, bta-miR-339b, and bta-miR-199b, which were analyzed for target gene prediction. Gene Ontology (GO) and KEGG pathway analyses indicated that these miRNAs target genes involved in transcription regulation, ubiquitin-dependent endoplasmic reticulum-associated degradation (ERAD) pathways, and signalling pathways. Functional exploration revealed that these genes play roles in spermatogenesis, motility, acrosome reactions, and inflammatory responses. qPCR analysis showed that bta-miR-195 had 80% higher expression in HF spermatozoa compared to LF, suggesting its association with fertility status (p < 0.05). In conclusion, this study elucidates the miRNA cargoes in SP-EVs as indicators of Sahiwal bull fertility, highlighting bta-miR-195 as a potential fertility factor among the various miRNAs identified.

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来源期刊
Frontiers in Cell and Developmental Biology
Frontiers in Cell and Developmental Biology Biochemistry, Genetics and Molecular Biology-Cell Biology
CiteScore
9.70
自引率
3.60%
发文量
2531
审稿时长
12 weeks
期刊介绍: Frontiers in Cell and Developmental Biology is a broad-scope, interdisciplinary open-access journal, focusing on the fundamental processes of life, led by Prof Amanda Fisher and supported by a geographically diverse, high-quality editorial board. The journal welcomes submissions on a wide spectrum of cell and developmental biology, covering intracellular and extracellular dynamics, with sections focusing on signaling, adhesion, migration, cell death and survival and membrane trafficking. Additionally, the journal offers sections dedicated to the cutting edge of fundamental and translational research in molecular medicine and stem cell biology. With a collaborative, rigorous and transparent peer-review, the journal produces the highest scientific quality in both fundamental and applied research, and advanced article level metrics measure the real-time impact and influence of each publication.
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