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RESEARCH PAPER / 2025-05-15

Exploring the relationship of transposable elements and ageing: causes and consequences.

Miriam Merenciano, Anaïs Larue, Chloé Garambois, William Vilas Boas Nunes, Cristina Vieira

Université Claude Bernard Lyon 1, Laboratoire de Biométrie et Biologie Evolutive, CNRS, UMR5558, Villeurbanne, 69100, France.Université Claude Bernard Lyon 1, Laboratoire de Biométrie et Biologie Evolutive, CNRS, UMR5558, Villeurbanne, 69100, France. · pubmed

Abstract

Ageing is a gradual biological process marked by a decline in physiological function, increasing susceptibility to disease, and mortality. Transposable elements (TEs) are repetitive DNA sequences capable of moving within the genome, and thus potentially inducing mutations and disrupting normal cellular functions. Their mobile nature contributes to genomic variation, as transposition events can alter gene expression, chromosome structure, and the epigenetic landscape. To mitigate TE-induced damage, cells rely on epigenetic mechanisms, such as DNA methylation, histone modifications and small RNAs, to repress TE activity. However, these silencing mechanisms become less effective with age, leading to increased TE activation. This review explores the dual role of TEs as both a cause and consequence of ageing, suggesting a complex relationship between TEs and the ageing process.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The paper suggests that transposable elements contribute to the ageing process through their activation and the resulting genomic instability. This research is relevant as it explores potential root causes of ageing, focusing on the role of transposable elements in the decline of cellular function over time.

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