de Duve Institute, UCLouvain, Avenue Hippocrate, 1200, Brussels, Belgium.
Biogerontology. 2024 Apr;25(2):289-300. doi: 10.1007/s10522-023-10074-7. Epub 2023 Oct 21.
Born as an endosymbiont, the bacteria engulfed by the proto-eukaryotic cell more than 1.45 billion years ago progressively evolved as an important organelle with multiple interactions with the host cell. In particular, strong connections between mitochondria and the chromosome ends, the telomeres, led to propose a new theory of ageing in which dysfunctional telomeres and mitochondria are the main actors of a vicious circle reducing cell fitness and promoting cellular ageing. We review the evidences that oxidative stress and dysfunctional mitochondria damage telomeres and further discuss the interrelationship between telomere biology and mitochondria through the lens of telomerase which shuttles between the nucleus and mitochondria. Finally, we elaborate on the possible role of the mitochondrial genome on the inheritance of human telomere length through the expression of mitochondrial gene variants.
作为内共生体诞生的细菌,在 14.5 亿年前被原始真核细胞吞噬,逐渐进化为一个重要的细胞器,与宿主细胞进行多种相互作用。特别是,线粒体和染色体末端(端粒)之间的紧密联系导致了一种新的衰老理论的提出,即功能失调的端粒和线粒体是导致细胞适应性降低和促进细胞衰老的恶性循环的主要因素。我们回顾了氧化应激和功能失调的线粒体损伤端粒的证据,并进一步通过端粒酶探讨了端粒生物学和线粒体之间的相互关系,端粒酶在细胞核和线粒体之间穿梭。最后,我们详细阐述了线粒体基因组通过表达线粒体基因变异在人类端粒长度遗传中的可能作用。