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Despic, V.

Publications and source records attributed to Despic, V..

2 recordsLinked to original sources

Prediction and evaluation of Split-ORFs using Ribo-seq data

Split Open Reading frames (Split-ORFs) occur in transcripts containing at least two open reading frames, each encoding a part of the same full-length protein. These multiple open reading frames arise from alternatively spliced transcript isoforms. Understanding which genes make Split-ORFs, and in which cell types and under which conditions, would generate new insights into gene regulation. We previously published the Split-ORF pipeline, a computational tool that predicts candidate Split-ORFs from transcript sequences. Here, we present a new and improved version of the Split-ORF pipeline adding modules to analyze Ribo-seq data, calculate regions unique to the Split-ORF candidates, quantitatively assess Ribo-seq coverage in these regions, and perform candidate prioritization. Using this pipeline, we predicted more than 14,000 candidate Split-ORF transcripts from alternatively spliced human transcripts containing premature termination codons or retained introns. Hundreds of candidate Split-ORFs show significant Ribo-seq coverage across diverse cell types and diseases in at least one of the Split-ORFs, and 120 transcripts in both Split-ORFs. The candidate Split-ORF genes with significant Ribo-seq coverage are enriched for RNA-binding and RNA-processing functions and the majority of them encode RNA-binding proteins.

bioinformatics↗

iCLIP3: A streamlined, non-radioactive protocol for mapping protein-RNA interactions in cellular transcripts at single-nucleotide resolution

UV-C crosslinking and immunoprecipitation (CLIP)-based methods are the gold standard for identifying direct RNA binding protein (RBP) interaction sites on cellular RNA in vivo. Here, we describe individual-nucleotide resolution CLIP version 3 (iCLIP3), an optimized protocol for generating transcriptome-wide maps of RBP-RNA interaction sites at single-nucleotide resolution from low-input material. iCLIP3 introduces several key improvements over previous iCLIP variants, including rapid and safe infrared-based visualization of RBP-RNA complexes, silica column-based RNA isolation, and the incorporation of TruSeq adapter sequences with unique dual indexing. These modifications streamline library preparation, facilitate multiplexing, and enable concurrent sequencing of iCLIP3 libraries alongside unrelated RNA-seq libraries. In addition, we provide a detailed bioinformatics workflow for identifying crosslinking events and defining RBP binding sites. The complete protocol can be performed within 4-5 days, offering a robust and efficient approach for high-resolution mapping of RBP-RNA interactions. HighlightsO_LI3' RNA labeling with pCp-IR750 enables rapid infrared visualization of RBP-RNA complexes C_LIO_LISilica column-based RNA isolation improves efficiency and reproducibility C_LIO_LITruSeq adapters with unique dual indexing enable flexible and scalable multiplexing C_LIO_LIiCLIP3 generates high-quality libraries from ultra-low amounts of cellular material C_LI

genomics↗