Identification and characterization of host miRNAs that target the mouse mammary tumour virus (MMTV) genome.

IF 4.5 3区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Open Biology Pub Date : 2024-12-01 Epub Date: 2024-12-11 DOI:10.1098/rsob.240203
Bushra Gull, Waqar Ahmad, Jasmin Baby, Neena G Panicker, Thanumol Abdul Khader, Tahir A Rizvi, Farah Mustafa
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Abstract

The intricate interplay between viruses and hosts involves microRNAs (miRNAs) to regulate gene expression by targeting cellular/viral messenger RNAs (mRNAs). Mouse mammary tumour virus (MMTV), the aetiological agent of breast cancer and leukaemia/lymphomas in mice, provides an ideal model to explore how viral and host miRNAs interact to modulate virus replication and tumorigenesis. We previously reported dysregulation of host miRNAs in MMTV-infected mammary glands and MMTV-induced tumours, suggesting a direct interaction between MMTV and miRNAs. To explore this further, we systematically examined all potential interactions between host miRNAs and the MMTV genome using advanced prediction tools. Leveraging miRNA sequencing data from MMTV-expressing cells, we identified dysregulated miRNAs capable of targeting MMTV. Docking analysis validated the interaction of three dysregulated miRNAs with the MMTV genome, followed by confirmation with RNA immunoprecipitation assays. We further identified host targets of these miRNAs using mRNA sequencing data from MMTV-expressing cells. These findings should enhance our understanding of how MMTV replicates and interacts with the host to induce cancer in mice, a model important for cancer research. Given MMTV's potential zoonosis and association with human breast cancer/lymphomas, if confirmed, our work could further lead to novel miRNA-based antivirals/therapeutics to prevent possible MMTV transmission and associated cancers in humans.

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靶向小鼠乳腺肿瘤病毒(MMTV)基因组的宿主mirna的鉴定和表征
病毒和宿主之间复杂的相互作用涉及到microRNAs (miRNAs)通过靶向细胞/病毒信使rna (mrna)来调节基因表达。小鼠乳腺肿瘤病毒(MMTV)是小鼠乳腺癌和白血病/淋巴瘤的病原,为探索病毒和宿主mirna如何相互作用以调节病毒复制和肿瘤发生提供了理想的模型。我们之前报道了MMTV感染的乳腺和MMTV诱导的肿瘤中宿主mirna的失调,这表明MMTV和mirna之间存在直接相互作用。为了进一步探索这一点,我们使用先进的预测工具系统地检查了宿主mirna和MMTV基因组之间的所有潜在相互作用。利用来自MMTV表达细胞的miRNA测序数据,我们发现了能够靶向MMTV的失调miRNA。对接分析证实了三种失调的mirna与MMTV基因组的相互作用,随后用RNA免疫沉淀试验进行了证实。我们利用mmtv表达细胞的mRNA测序数据进一步确定了这些mirna的宿主靶点。这些发现应该加强我们对MMTV如何复制并与宿主相互作用诱导小鼠癌症的理解,这是癌症研究的一个重要模型。考虑到MMTV潜在的人畜共患病和与人类乳腺癌/淋巴瘤的关联,如果得到证实,我们的工作可能进一步导致新的基于mirna的抗病毒/治疗药物,以预防可能的MMTV在人类中的传播和相关癌症。
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来源期刊
Open Biology
Open Biology BIOCHEMISTRY & MOLECULAR BIOLOGY-
CiteScore
10.00
自引率
1.70%
发文量
136
审稿时长
6-12 weeks
期刊介绍: Open Biology is an online journal that welcomes original, high impact research in cell and developmental biology, molecular and structural biology, biochemistry, neuroscience, immunology, microbiology and genetics.
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