Ana Guerrero

Ageing is characterised by the accumulation of cellular damage. Among the biomarkers associated with this process are epigenetic ‘clocks’, which analyse non-genetic modifications of DNA over time. However, these approaches have certain limitations, as they do not reflect the activity of specific genes. Now, a study published in Nature has analysed more than 11,000 transcriptomes from over 25 tissues in mice, rats, macaques and humans, showing that ageing-associated changes are conserved across species and cell types. The findings reveal universal transcriptomic signatures of ageing and mortality in mammals. Using these data, the authors developed their own molecular ‘clocks’, capable of estimating biological age and expected mortality.

A technique developed under the coordination of researchers from the Centre for Genomic Regulation (CRG) and the Institute for Biomedical Research (IRB) in Barcelona has made it possible to track methylation patterns or “barcodes” in blood cells and construct their epigenetic family tree. This has enabled them to trace their evolution and changes with age, which could be useful for disease prevention and for the study or even development of specific therapies against ageing. The results are published in the journal Nature.