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de la Vega-Barranco, G.

Publications and source records attributed to de la Vega-Barranco, G..

3 recordsLinked to original sources

lisaR: An LLM-Inferred Semantic Annotation of biological categories for gene set enrichment analysis

Gene set enrichment analysis (GSEA) turns differential expression results into lists of enriched gene sets. These lists are often long and redundant and span several gene-set collections, which makes their biological interpretation difficult. We present lisaR, an R package that reads previously computed differential expression or differential abundance results, runs GSEA and organises the output with the LISA dictionaries (LLM-Inferred Semantic Annotation). The dictionaries place 13,511 gene sets from the three Gene Ontology branches and from curated pathway collections such as Reactome, WikiPathways, KEGG, BioCarta and PID in 158 biological categories grouped into 42 supercategories within four dictionaries. Four open-weight language models scored the semantic fit of each gene set to the categories, and a consensus rule selected the assignments. The dictionaries are distributed with the package and do not depend on the data: studies analysed at different times with the same dictionaries are interpreted with the same categories, and no language model is queried during an analysis. For each category, lisaR summarises the direction of its significant gene sets and applies closed testing with Hommel's robust procedure, which states whether the category shows evidence of enrichment and gives a simultaneous lower bound on how many of its gene sets are enriched. lisaR results are summarised in a report that opens in a web browser and leads from each category to its gene sets and genes, with every figure saved together with its data and R code. We illustrate the workflow with RNA-seq from melanoma biopsies taken before and during nivolumab treatment and with paired tumour and adjacent-tissue proteomics from clear cell renal cell carcinoma. Availability: lisaR is available at https://github.com/DBM-OlmedaLab/lisaR and archived at https://doi.org/10.5281/zenodo.23044930; documentation at https://olmedalab.org/lisaR/.

bioinformatics↗

The accumulation of orphan ribosomal proteins is a hallmark of ALS

Amyotrophic lateral sclerosis (ALS) is a progressive neurodegenerative disease of poor prognosis, for which age is the strongest risk factor. Despite significant progress in the discovery of ALS-associated mutations, no model explains how such a diversity of mutations converges in a common pathology. In addition, most ALS cases are sporadic and lack known genetic drivers. We recently reported that arginine-rich peptides arising from the C9ORF72 mutation trigger a widespread accumulation of orphan ribosomal proteins (oRP). Here, we show that oRP accumulation is also observed upon expression of other RNA-related ALS mutations, such as hnRNPA2D290V and TDP-43A315T, as well as upon exposure to the ALS-related neurotoxin {beta}-N-methylamino-L-alanine (BMAA). Furthermore, the transcriptional signature of patients with sporadic ALS resembles that of Diamond-Blackfan anemia (DBA), a known ribosomopathy. Supporting the usefulness of our in vitro data, a transcriptional signature defined from these models provides diagnostic and prognostic value in ALS patients. We propose that the accumulation of oRPs due to dysfunctional ribosome biogenesis is a molecular hallmark of ALS that can contribute to the progressive loss of motor neurons in the disease.

neuroscience↗

VCP/p97 extracts DNA polymerase alfa/Primase from chromatin to limit the activation of the replication stress response

The replication stress response is an essential pathway that deals with the obstacles that halt the progression of DNA replication forks even during an unperturbed S phase. Basal activation of the ATR and CHK1 kinases prevents the premature firing of origins of replication during S phase, avoiding the activation of an excessive number of replication forks and the appearance of genomic instability. However, the mechanisms that regulate ATR activation in the unperturbed S phase have not been fully determined. Here we present evidence that the AAA ATPase VCP/p97 regulates the presence of the DNA polymerase /Primase complex (POLA/PRIM) on chromatin, thus limiting its activity and hampering the subsequent activation of ATR by TOPBP1. As a consequence, inhibiting VCP/p97 activates ATR and CHK1 and leads to a cell cycle arrest in G2/M. We propose that the priming activity of POLA/PRIM in the lagging strand is one of the determinants of the basal activation of ATR during an unperturbed S phase and VCP/p97 limits this activation through the extraction of POLA/PRIM from chromatin.

molecular biology↗