Literature DB >> 15619469

The role of ubiquinone in Caenorhabditis elegans longevity.

Juan Carlos Rodríguez-Aguilera1, Angela Gavilán, Claudio Asencio, Plácido Navas.   

Abstract

Aging is an irreversible physiological process that affects all living organisms. Different mutations in the insulin signaling pathway and caloric restriction have been shown to retard aging in Caenorhabditis elegans. In addition, mutations or RNAi silencing of components of the respiratory chain results in the modification of adult life span. Another class of genes that affect life span in C. elegans is the clock (clk) genes. Particularly interesting is clk-1, which encodes an enzyme required for ubiquinone (coenzyme Q, CoQ) biosynthesis. Down-regulation by RNAi silencing of the genes required for ubiquinone biosynthesis also extends life span in C. elegans, and CoQ supplied in the diet also affects nematode longevity in both clk-1 and wild-type strains. Although there are many aspects that can be considered in aging, we focus this review on the role of CoQ in the longevity of C. elegans. We will review the current information about the biosynthesis of CoQ and its dietary supplementation related to the extension of life span. We will also analyze the function of CoQ in the electron transport chain and reactive oxygen species production in the context of aging. We hypothesize that the role of CoQ on longevity of C. elegans supports the oxidative damage theory of aging.

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Year:  2004        PMID: 15619469     DOI: 10.1016/j.arr.2004.09.001

Source DB:  PubMed          Journal:  Ageing Res Rev        ISSN: 1568-1637            Impact factor:   10.895


  8 in total

1.  Ubiquinone synthesis in mitochondrial and microsomal subcellular fractions of Pneumocystis spp.: differential sensitivities to atovaquone.

Authors:  Mireille Basselin; Shannon M Hunt; Hiam Abdala-Valencia; Edna S Kaneshiro
Journal:  Eukaryot Cell       Date:  2005-08

2.  Missense mutation of the COQ2 gene causes defects of bioenergetics and de novo pyrimidine synthesis.

Authors:  José M López-Martín; Leonardo Salviati; Eva Trevisson; Giovanni Montini; Salvatore DiMauro; Catarina Quinzii; Michio Hirano; Angeles Rodriguez-Hernandez; Mario D Cordero; José A Sánchez-Alcázar; Carlos Santos-Ocaña; Plácido Navas
Journal:  Hum Mol Genet       Date:  2007-03-20       Impact factor: 6.150

3.  The UPRmt Protects Caenorhabditis elegans from Mitochondrial Dysfunction by Upregulating Specific Enzymes of the Mevalonate Pathway.

Authors:  Olga Oks; Shany Lewin; Irina Langier Goncalves; Amir Sapir
Journal:  Genetics       Date:  2018-03-29       Impact factor: 4.562

4.  Coenzyme Q protects Caenorhabditis elegans GABA neurons from calcium-dependent degeneration.

Authors:  Laurie R Earls; Mallory L Hacker; Joseph D Watson; David M Miller
Journal:  Proc Natl Acad Sci U S A       Date:  2010-07-27       Impact factor: 11.205

5.  Elevated CO2 levels affect development, motility, and fertility and extend life span in Caenorhabditis elegans.

Authors:  Kfir Sharabi; Anat Hurwitz; Amos J Simon; Greg J Beitel; Richard I Morimoto; Gideon Rechavi; Jacob I Sznajder; Yosef Gruenbaum
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-23       Impact factor: 11.205

6.  An elt-3/elt-5/elt-6 GATA transcription circuit guides aging in C. elegans.

Authors:  Yelena V Budovskaya; Kendall Wu; Lucinda K Southworth; Min Jiang; Patricia Tedesco; Thomas E Johnson; Stuart K Kim
Journal:  Cell       Date:  2008-07-25       Impact factor: 41.582

7.  Expression of the rDNA-encoded mitochondrial protein Tar1p is stringently controlled and responds differentially to mitochondrial respiratory demand and dysfunction.

Authors:  Nicholas D Bonawitz; Marc Chatenay-Lapointe; Christopher M Wearn; Gerald S Shadel
Journal:  Curr Genet       Date:  2008-07-12       Impact factor: 3.886

8.  Effects of inhibiting CoQ10 biosynthesis with 4-nitrobenzoate in human fibroblasts.

Authors:  Catarina M Quinzii; Saba Tadesse; Ali Naini; Michio Hirano
Journal:  PLoS One       Date:  2012-02-16       Impact factor: 3.240

  8 in total

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