Mitochondria, its DNA and telomeres in ageing and human population

Egija Zole, Renāte Ranka

Research output: Contribution to journalReview articlepeer-review

15 Citations (Scopus)

Abstract

In the last decades, studies about ageing have become more essential as our population grows older. The incidence of age-related diseases increases, which pose challenges both for societies and individuals in terms of life quality and economic impact. Understanding ageing and ageing-related processes will help us to slow down or even prevent these diseases and provide opportunities for healthy ageing; additionally, we all want to live longer. Ageing is a consequence of the interaction between processes that occur over time and genetics interacting with various disease states and an individual’s lifestyle. There are several hallmarks of ageing that are generally accepted, but neither of the theories appears to be fully satisfactory. The focus of this article is on two theories of ageing: telomere shortening and mitochondrial DNA (mtDNA) alterations and dysfunction. We discuss characteristic molecular features such as mitochondrial haplogroups, telomere length, mtDNA copy number and heteroplasmy, and how all these traits come together in the ageing population. The recent evidence shows the existence of a strong linkage between these two theories suggesting common molecular mechanisms and a complicated telomere-mitochondria interplay during the humans’ ageing. However, this relationship is still not completely understood, which is why it needs more attention.

Original languageEnglish
Pages (from-to)189-208
JournalBiogerontology
Volume19
Issue number3/4
DOIs
Publication statusPublished - 1 Jul 2018

Keywords*

  • Heteroplasmy
  • Mitochondrial haplogroups
  • mtDNA copy number
  • Population ageing
  • Telomere length

Field of Science*

  • 3.1 Basic medicine
  • 1.6 Biological sciences
  • 3.3 Health sciences

Publication Type*

  • 1.1. Scientific article indexed in Web of Science and/or Scopus database

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