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As part of our commitment with society, the Institute of Evolutionary Biology (IBE, CSIC-UPF) wants to give credit and visibility to the achievements of female scientists in evolution. 

To that aim, we launched the campaign #WhoisyourSHEro to share stories of women who had an impact in our researchers' scientific career through our social media and website.

The campaign keeps on moving as more and more women in evolution are inspiring the IBE community.

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Back Evolutionary analysis of RNA processing landscapes in the primate lineage

Evolutionary analysis of RNA processing landscapes in the primate lineage

The study, published in Genome Research, has tackled the analysis of the evolution of RNA diversity in humans and our closely related species.

The authors have produced the largest isoform catalogue in primates to date, disclosing thousands of novel isoforms produced by well-characterized genes, but also by novel genes.

They have uncovered a widespread similarity in RNA diversity across primates, with only some species-specific RNA products.

26.08.2022

The genetic instructions for organisms to grow, self-maintain and reproduce are rooted in their genomes. Under certain conditions, genes are activated to produce a number of RNA molecules that, once processed, lead to different versions of the gene in question (RNA isoforms) and will potentially be used as a template to synthesize proteins. Due to their biological significance, RNA processing events are considered to play a major role in the evolution of distinct species. However, their impact in recent human evolution is largely unknown.

The project, led by David de Juan and Tomàs Marquès-Bonet at the Institute of Evolutionary Biology (IBE), a joint research centre of the Spanish National Research Council (CSIC) and Pompeu Fabra University (UPF), together with Guojie Zhang (BGI Shenzhen), recently published in Genome Research, has tackled the analysis of the evolution of RNA diversity in humans and our closely related species. They focused on the molecular characterization of lymphoblastoid cell lines from multiple primates (human, chimpanzee, gorilla, orangutan and rhesus macaque), which represent a suitable model system to compare their gene regulation architectures under very controlled experimental conditions.

To do so, they took advantage of cutting-edge sequencing technology that captures RNA isoforms with single-molecule resolution, while previous methods only sequence small RNA fragments that are used to reassemble the puzzle. “The so-called long-read sequencing technologies skip the computational inference of isoforms, which is a very error-prone process. In this way, isoforms can be directly compared across species to know if they are shared or exclusive to a certain lineage”, says Luis Ferrández-Peral, IBE researcher at the Comparative Genomics Lab at IBE and first author of the article.

In this work, the authors have produced the largest isoform catalogue in primates to date, disclosing thousands of novel isoforms produced by well-characterized genes, but also by novel genes. “Around half of these RNA isoforms are not present in public databases, meaning that gold-standard repositories commonly used in genome research are missing a significant fraction of gene products”, adds Tomàs Marquès-Bonet.

Their comparative analyses uncovered a widespread similarity in RNA diversity across primates, with only some species-specific RNA products. These evolutionary innovations are mainly involved in the innate immune system and inflammatory pathways. “These RNA changes usually preserve the function of the protein, representing a source of subtle regulatory fine-tuning. In this study, we are providing the foundations for future research on the role of transcriptome evolution in the processes of immune response, cell proliferation and differentiation in the primate lineage”, states David de Juan.

Reference article: Ferrández-Peral et al. Transcriptome innovations in primates revealed by single-molecule long-read sequencing. Genome Research, August 2022.  DOI: https://genome.cshlp.org/content/early/2022/08/09/gr.276395.121 http://www.doi.org/10.1101/gr.276395.121