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

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Publicado en:BMC Genomics vol. 26 (2025), p. 1-24
Autor principal: Pluta, Aneta
Otros Autores: Droscha, Casey
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Springer Nature B.V.
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Acceso en línea:Citation/Abstract
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024 7 |a 10.1186/s12864-025-12074-y  |2 doi 
035 |a 3268438618 
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100 1 |a Pluta, Aneta 
245 1 |a Identification of novel RNA polymerase III promoters in bovine leukemia virus miRNA cluster by cross-taxa analysis of small non-coding RNAs 
260 |b Springer Nature B.V.  |c 2025 
513 |a Journal Article 
520 3 |a BackgroundBovine 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.ResultsHere, 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.ConclusionsDespite 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. 
653 |a Leukemia 
653 |a RNA polymerase 
653 |a Promoters 
653 |a miRNA 
653 |a Ribonucleic acid--RNA 
653 |a Leukosis 
653 |a MicroRNAs 
653 |a Viruses 
653 |a Reptiles & amphibians 
653 |a Genomes 
653 |a Non-coding RNA 
653 |a Clusters 
653 |a Genomics 
653 |a Genes 
653 |a Degeneration 
653 |a DNA-directed RNA polymerase 
653 |a Transfer RNA 
653 |a Lymphocytes 
653 |a Nucleotides 
653 |a Bovine leukosis 
653 |a Invertebrates 
653 |a Cattle 
653 |a Environmental 
700 1 |a Droscha, Casey 
773 0 |t BMC Genomics  |g vol. 26 (2025), p. 1-24 
786 0 |d ProQuest  |t Health & Medical Collection 
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