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Ontiveros-Palacios, N.

Publications and source records attributed to Ontiveros-Palacios, N..

3 recordsLinked to original sources

Viral non-coding RNA structure annotation and API-based data retrieval with Rfam and R2DT

Rfam is a comprehensive database of non-coding RNA (ncRNA) families providing curated sequence alignments, consensus secondary structures, and covariance models for thousands of RNA families. The database is essential for identifying structured non-coding RNAs in newly sequenced genomes and understanding RNA structure-function relationships. Here we present computational protocols for automated ncRNA annotation of viral genomes, and for programmatic interaction with Rfam through its RESTful API. We showcase genome-wide RNA structure visualization from a genome sequence and from a multiple sequence alignment by generating comprehensive 2D structure diagrams using newly developed features in R2DT. We also present practical examples for retrieving family metadata, downloading alignments, accessing secondary structures, and searching user sequences from the Rfam API. These methods enable researchers in virology and RNA biology to integrate Rfam data into custom bioinformatics pipelines, comparative analyses, and machine learning workflows.

bioinformatics↗

First full-genome alignment representative for the genus Pestivirus

The members of the genus Pestivirus in the family Flaviviridae comprise economically important pathogens of life stock like classical swine fever (CSFV) and bovine viral diarrhea virus (BVDV). Intense research over the last years revealed that at least 11 recognized and eight proposed pestivirus species exist. The single-stranded, positive-sense RNA genome encodes for one large polyprotein which is processed by viral and cell-derived proteases into 12 mature proteins. Besides its protein-coding function, the RNA genome also contains RNA secondary structures with critical importance for various stages of the viral life cycle. Some of those RNA secondary structures, like the internal ribosome entry site (IRES) and a 3 stem-loop essential for genome replication, had already been studied for a few individual pestiviruses. In this study, we provide the first genome-wide multiple sequence alignment (MSA) including all known pestivirus species (accepted and tentative). Moreover, we performed a comprehensive analysis of RNA secondary structures phylogenetically conserved across the complete genus. While showing well-described structures, like a 5 stem-loop structure, the IRES element, and the 3 stem loop SL I to be conserved between all pestiviruses, other RNA secondary structures in the 3 untranslated region (UTR) were only conserved in subsets of the species. We identified 29 novel phylogenetically conserved RNA secondary structures in the protein-coding region, with so far unresolved functional importance. The microRNA binding site for miR-17 was previously known in species A, B, and C; in this study, we identified it in ten additional species, but not in species K, S, Q, and R. Another interesting finding is the identification of a putative long-distance RNA interaction between the IRES and the 3 end of the genome. These results together with the now available comprehensive multiple sequence alignment including all 19 pestivirus species, represent a valuable resource for future research and diagnostic purposes.

bioinformatics↗

Rfam 15: RNA families database in 2025

The Rfam database, a widely-used repository of non-coding RNA (ncRNA) families, has undergone significant updates in release 15.0. This paper introduces major improvements, including the expansion of Rfamseq to 26, 106 genomes, a 76% increase, incorporating the latest UniProt reference proteomes and additional viral genomes. Sixty-five RNA families were enhanced using experimentally determined 3D structures, improving the accuracy of consensus secondary structures and annotations. R-scape covariation analysis was used to refine structural predictions in 26 families. Gene Ontology and Sequence Ontology annotations were comprehensively updated, increasing GO term coverage to 75% of families. The release adds 14 new Hepatitis C Virus RNA families and completes microRNA family synchronisation with miRBase, resulting in 1, 603 microRNA families. New data types, including FULL alignments, have been implemented. Integration with APICURON for improved curator attribution and multiple website enhancements further improve user experience. These updates significantly expand Rfams coverage and improve annotation quality, reinforcing its critical role in RNA research, genome annotation, and the development of machine learning models. Rfam is freely available at https://rfam.org. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=112 SRC="FIGDIR/small/614430v1_ufig1.gif" ALT="Figure 1"> View larger version (33K): org.highwire.dtl.DTLVardef@9b1898org.highwire.dtl.DTLVardef@6bc030org.highwire.dtl.DTLVardef@16b789org.highwire.dtl.DTLVardef@16b8577_HPS_FORMAT_FIGEXP M_FIG Rfam has undergone a major update with the release of 15.0. We have increased the number of genomes in our sequence database Rfamseq by 75%, completed the synchronisation with miRBase and improved 65 families using 3D structures. C_FIG

genomics↗