Literature DB >> 12200038

The variability of the mitochondrial genome in human aging: a key for life and death?

G Rose1, G Passarino, C Franceschi, G De Benedictis.   

Abstract

The impressive performance of the research in mitochondrial genetics and human aging in the last decade outlines a new scenery in which the inherited variation of the mitochondrial genome (mtDNA) may play a role in rate and quality of aging. This variation in humans was initially looked at as nearly neutral, and useful just for the reconstruction of human population history. However, recent data suggest that different mtDNA molecules are qualitatively different from each other. The aim of this paper is to discuss current ideas on the relationships among mitochondrial function, mtDNA inherited variation, and aging. The main processes where the mitochondrion is involved and the importance these processes have on aging and death of individuals will be described. A possible connection between programmed death phenomena (mitoptosis, apoptosis, phenoptosis) and rate and quality of aging will be discussed. Finally, the possible role played in these processes by the mtDNA germline variation will be explored.

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Year:  2002        PMID: 12200038     DOI: 10.1016/s1357-2725(02)00042-0

Source DB:  PubMed          Journal:  Int J Biochem Cell Biol        ISSN: 1357-2725            Impact factor:   5.085


  7 in total

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3.  Low-dose testosterone treatment decreases oxidative damage in TM3 Leydig cells.

Authors:  Thomas I S Hwang; Tien-Ling Liao; Ji-Fan Lin; Yi-Chia Lin; Shu-Yu Lee; Yen-Chun Lai; Shu-Huei Kao
Journal:  Asian J Androl       Date:  2011-02-07       Impact factor: 3.285

4.  Human aging and somatic point mutations in mtDNA: A comparative study of generational differences (grandparents and grandchildren).

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5.  Sequence-based polymorphisms in the mitochondrial D-loop and potential SNP predictors for chronic dialysis.

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Review 6.  Human longevity: Genetics or Lifestyle? It takes two to tango.

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7.  The co-occurrence of mtDNA mutations on different oxidative phosphorylation subunits, not detected by haplogroup analysis, affects human longevity and is population specific.

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Journal:  Aging Cell       Date:  2013-12-17       Impact factor: 9.304

  7 in total

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