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Biology subjects

Gomez-Cabello, D.

Publications and source records attributed to Gomez-Cabello, D..

4 recordsLinked to original sources

PERREO: An integrated pipeline for repetitive elements analysis enables the repeatome expression profiling in cancer

Transcriptome-wide profiling of repetitive elements expression reveals transposable element-derived transcripts that are deregulated in diverse biological contexts including cancer. However, most RNA-seq pipelines are optimized for annotated genes and substantially undercount repeat RNA molecules, limiting their discovery and characterization. Here we present PERREO, a comprehensive, user-friendly pipeline for analyzing repetitive RNA elements from short- and long-read sequencing data. PERREO performs quality control, repeat-aware alignment and quantification, differential expression analysis, co-expression network analysis, and de novo transcript assembly with minimal computational expertise required. We validate PERREO across cell lines, tumor tissues and liquid biopsies, demonstrating superior sensitivity to repetitive RNA signatures compared with standard RNA-seq approaches. PERREO integrates predictive modelling to identify biological associations and generates publication-ready visualizations. By removing the bioinformatic barrier to repetitive RNA discovery, this pipeline enables broader investigation of the repeatomes role in cellular biology and disease, yielding valuable results that, for specific analytical objectives, outperform certain existing tools and pipelines.

bioinformatics↗

RNA Polymerase II-mediated transcription is required for repair of ribosomal DNA breaks in nucleolar caps, guarding against genomic instability

Ribosomal DNA (rDNA) double-strand breaks (DSBs) threaten genome integrity due to the repetitive and transcriptionally active nature of rDNA. The nucleolus, while central to ribosome biogenesis, also functions as stress sensor. Here, we identify a transcription-dependent mechanism in which RNA polymerase II (RNAPII) is essential for homologous recombination (HR) repair of rDNA DSBs. Using CRISPR-induced breaks, high-resolution imaging, and transcriptional inhibition, we show that RNAPII activity drives the formation of nucleolar repair caps. Mechanistically, CtIP promotes RNAPII recruitment and H3K36 trimethylation at rDNA lesions, facilitating HR. Disruption of this RNAPII-CtIP-H3K36me3 axis impairs cap formation and repair, leading to persistent damage. RNAPII inhibition exacerbates genome instability and synergizes with rDNA breaks to induce cancer cell death, without acutely impairing ribosome function. These findings uncover a co-transcriptional mechanism of rDNA repair and highlight RNAPII-mediated chromatin remodeling and spatial reorganization as key to nucleolar genome maintenance and potential targets for cancer therapy. TeaserNascent RNA synthesis by RNAPII safeguards ribosomal DNA integrity to avoid genomic instability in human cells. Graphical Abstract O_FIG O_LINKSMALLFIG WIDTH=137 HEIGHT=200 SRC="FIGDIR/small/563274v2_ufig1.gif" ALT="Figure 1"> View larger version (31K): org.highwire.dtl.DTLVardef@8e9b03org.highwire.dtl.DTLVardef@63116eorg.highwire.dtl.DTLVardef@d583dorg.highwire.dtl.DTLVardef@1c2eab_HPS_FORMAT_FIGEXP M_FIG C_FIG

cell biology↗

CtIP-dependent nascent RNA expression flanking DNA breaks guides the choice of DNA repair pathway

The RNA world is changing our views about sensing and resolution of DNA damage. Here, we developed single-molecule DNA/RNA analysis approaches to visualize how nascent RNA facilitates the repair of DNA double-strand breaks (DSBs). RNA polymerase II (RNAPII) is crucial for DSB resolution in human cells. DSB-flanking, RNAPII-generated nascent RNA forms RNA:DNA hybrids, guiding the upstream DNA repair steps towards favouring the error-free Homologous Recombination (HR) pathway over Non-Homologous End Joining. Specific RNAPII inhibitor, THZ1, impairs recruitment of essential HR proteins to DSBs, implicating nascent RNA in DNA end resection, initiation and execution of HR repair. We further propose that resection factor CtIP interacts with and re-activates RNAPII when paused by the RNA:DNA hybrids, collectively promoting faithful repair of chromosome breaks to maintain genomic integrity.

molecular biology↗

RAD51 paralogs regulate double strand break repair pathway choice by limiting Ku complex retention

RAD51 paralogs are a group of conserved proteins in eukaryotes that are involved in the repair of DNA breaks at several levels. On one hand, they help the strand invasion step catalyzed by RAD51. Also, they play late roles in Holliday Junction metabolism. Here we uncover a new role of the RAD51 paralogs at an earlier event in the repair of broken chromosomes. All five RAD51 paralogs affect the balance between double strand break repair pathways. Specifically, they favor homology-mediated repair over non-homologous end-joining. Such role is independent of RAD51 or the checkpoint activity of these proteins. Moreover, it defines a novel control point of double strand break repair independent and subsequent to DNA-end resection initiation.\n\nMechanistically, RAD51 paralogs limit the retention of Ku80 at the sites of DNA breaks. Thus, our data extend the role of this family of proteins to the earliest event of double strand break repair.

molecular biology↗