Merenciano Miriam, Larue Anaïs, Garambois Chloé, Nunes William Vilas Boas, Vieira Cristina
Laboratoire de Biométrie et Biologie Evolutive, CNRS, UMR5558, Université Claude Bernard Lyon 1, Villeurbanne 69100, France.
INRAE, BF2I, UMR203, INSA Lyon, Villeurbanne 69621, France.
Genome Biol Evol. 2025 May 30;17(6). doi: 10.1093/gbe/evaf088.
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.
衰老是一个渐进的生物学过程,其特征是生理功能下降、对疾病的易感性增加以及死亡率上升。转座元件(TEs)是能够在基因组内移动的重复DNA序列,因此有可能诱发突变并破坏正常细胞功能。它们的移动特性导致了基因组变异,因为转座事件可以改变基因表达、染色体结构和表观遗传格局。为了减轻TEs诱导的损伤,细胞依靠表观遗传机制,如DNA甲基化、组蛋白修饰和小RNA,来抑制TEs的活性。然而,这些沉默机制随着年龄的增长而变得不那么有效,导致TEs的激活增加。这篇综述探讨了TEs作为衰老的原因和结果的双重作用,表明TEs与衰老过程之间存在复杂的关系。