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Biomedical

MtDNA deletions and aging

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Charlotte Sprason,

Charlotte Sprason


Trudy Tucker,

Trudy Tucker


David Clancy

David Clancy


  Peer Reviewed

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© attribution CC-BY

  • 0

rating
445 Views

Added on

2024-10-26

Doi: http://dx.doi.org/10.3389/fragi.2024.1359638

Related Subjects
Anatomy
Biochemistry
Epidemiology
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Pathology
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Physiology
Psychiatry
Primary care
Women and reproductive health

Abstract

Aging is the major risk factor in most of the leading causes of mortality worldwide, yet its fundamental causes mostly remain unclear. One of the clear hallmarks of aging is mitochondrial dysfunction. Mitochondria are best known for their roles in cellular energy generation, but they are also critical biosynthetic and signaling organelles. They also undergo multiple changes with organismal age, including increased genetic errors in their independent, circular genome. A key group of studies looking at mice with increased mtDNA mutations showed that premature aging phenotypes correlated with increased deletions but not point mutations. This generated an interest in mitochondrial deletions as a potential fundamental cause of aging. However, subsequent studies in different models have yielded diverse results. This review summarizes the research on mitochondrial deletions in various organisms to understand their possible roles in causing aging while identifying the key complications in quantifying deletions across all models.

Key Questions

What are mitochondrial DNA (mtDNA) deletions?

mtDNA deletions are mutations where segments of the mitochondrial genome are lost, leading to dysfunctional mitochondria. These deletions can accumulate over time, potentially impairing cellular energy production and contributing to aging. :contentReference[oaicite:1]{index=1}

How do mtDNA deletions relate to aging?

Accumulation of mtDNA deletions over time can lead to mitochondrial dysfunction, which is a hallmark of aging. This dysfunction may contribute to age-related diseases and the overall aging process by impairing cellular energy metabolism. :contentReference[oaicite:2]{index=2}

What challenges exist in studying mtDNA deletions and aging?

Quantifying mtDNA deletions is complex due to their heterogeneous nature and the difficulty in detecting low-abundance mutations. Additionally, the diverse results across different models highlight the need for standardized methodologies to assess the impact of mtDNA deletions on aging. :contentReference[oaicite:3]{index=3}

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ARTICLE USAGE


Article usage: Oct-2024 to May-2025
Show by month Manuscript Video Summary
2025 May 92 92
2025 April 67 67
2025 March 59 59
2025 February 48 48
2025 January 47 47
2024 December 68 68
2024 November 47 47
2024 October 17 17
Total 445 445
Show by month Manuscript Video Summary
2025 May 92 92
2025 April 67 67
2025 March 59 59
2025 February 48 48
2025 January 47 47
2024 December 68 68
2024 November 47 47
2024 October 17 17
Total 445 445
Related Subjects
Anatomy
Biochemistry
Epidemiology
Genetics
Neuroscience
Psychology
Oncology
Medicine
Musculoskeletal science
Pediatrics
Pathology
Pharmacology
Physiology
Psychiatry
Primary care
Women and reproductive health
copyright icon

© attribution CC-BY

  • 0

rating
445 Views

Added on

2024-10-26

Doi: http://dx.doi.org/10.3389/fragi.2024.1359638

Related Subjects
Anatomy
Biochemistry
Epidemiology
Genetics
Neuroscience
Psychology
Oncology
Medicine
Musculoskeletal science
Pediatrics
Pathology
Pharmacology
Physiology
Psychiatry
Primary care
Women and reproductive health

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