Identification of novel RNA polymerase III promoters in bovine leukemia virus miRNA cluster by cross-taxa analysis of small non-coding RNAs.

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Aneta Pluta, Casey Droscha
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引用次数: 0

Abstract

Background: Bovine leukemia virus (BLV) is an oncogenic deltaretrovirus that induces enzootic bovine leukosis. A defining feature of BLV is its viral miRNA cluster, which is transcribed atypically by RNA polymerase III via internal type 2 promoters rather than through the canonical Pol II pathway. These miRNAs accumulate to high levels within infected lymphocytes and can alter expression of a variety of host genes involved in lymphocyte proliferation and impose leukemogenic processes.

Results: Here, we present a comprehensive in silico characterization of new A-box and B-box promoter motifs within the BLV miRNA-coding region. As the first step, a taxonomically diverse dataset of small non-coding RNAs (tRNAs, SINEs, and other ncRNAs) was assembled to derive position-weight matrices and corresponding IUPAC consensus sequences for type 2 internal Pol III promoter motifs. Using these models, all available BLV miRNA cluster sequences were scanned to identify and map A-box-like and B-box-like elements and to reconstruct the underlying promoter architecture. Our analyses reveal a noncanonical BLV promoter organization: overlapping degenerate A-box variants-most frequently three distinct elements-reside within the pre-miRNA hairpin region, whereas B-box elements were positioned downstream of the Pol III termination signal, effectively excluded from the mature transcript.

Conclusions: Despite motif degeneration, critical nucleotide positions remained strongly conserved, indicating evolutionary pressure to preserve Pol III recruitment while accommodating viral genome constraints. These findings fill a crucial gap in understanding of BLV Pol III promoter architecture and provide a foundation for future studies on how unconventional promoter configurations regulate viral miRNA expression and virus-host interactions.

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牛白血病病毒miRNA簇新型RNA聚合酶III启动子的跨分类分析
背景:牛白血病病毒(BLV)是一种致癌的三角逆转录病毒,可诱导牛地方性白血病。BLV的一个决定性特征是其病毒miRNA簇,其非典型地通过RNA聚合酶III通过内部2型启动子而不是通过典型的Pol II途径进行转录。这些mirna在感染淋巴细胞内积累到高水平,可以改变参与淋巴细胞增殖和施加白血病发生过程的多种宿主基因的表达。结果:在这里,我们展示了BLV mirna编码区内新的a -box和B-box启动子基序的全面硅表征。作为第一步,组装了一个分类多样化的小非编码rna (trna, sin和其他ncrna)数据集,以获得2型内部Pol III启动子基序的位置-权重矩阵和相应的IUPAC共识序列。利用这些模型,对所有可用的BLV miRNA簇序列进行扫描,以识别和绘制A-box-like和B-box-like元件,并重建底层启动子结构。我们的分析揭示了一种非规范的BLV启动子组织:重叠的退化a -box变体(最常见的是三个不同的元件)位于前mirna发夹区,而B-box元件位于Pol III终止信号的下游,有效地排除在成熟转录物之外。结论:尽管基序退化,但关键核苷酸位置仍然高度保守,表明在适应病毒基因组限制的同时保持Pol III募集的进化压力。这些发现填补了对BLV Pol III启动子结构理解的重要空白,并为未来研究非常规启动子结构如何调节病毒miRNA表达和病毒与宿主相互作用提供了基础。
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
BMC Genomics
BMC Genomics 生物-生物工程与应用微生物
CiteScore
7.40
自引率
4.50%
发文量
769
审稿时长
6.4 months
期刊介绍: BMC Genomics is an open access, peer-reviewed journal that considers articles on all aspects of genome-scale analysis, functional genomics, and proteomics. BMC Genomics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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