Literature DB >> 10767577

Forward and reverse selection for longevity in Drosophila is characterized by alteration of antioxidant gene expression and oxidative damage patterns.

R Arking1, V Burde, K Graves, R Hari, E Feldman, A Zeevi, S Soliman, A Saraiya, S Buck, J Vettraino, K Sathrasala, N Wehr, R L Levine.   

Abstract

Patterns of antioxidant gene expression and of oxidative damage were measured throughout the adult life span of a selected long-lived strain (La) of Drosophila melanogaster and compared to that of their normal-lived progenitor strain (Ra). Extended longevity in the La strain is correlated with enhanced antioxidant defense system gene expression, accumulation of CuZnSOD protein, and an increase in ADS enzyme activities. Extended longevity is strongly associated with a significantly increased resistance to oxidative stress. Reverse-selecting this long-lived strain for shortened longevity (RevLa strain) yields a significant decrease in longevity accompanied by reversion to normal levels of its antioxidant defense system gene expression patterns and antioxidant enzyme patterns. The significant effects of forward and reverse selection in these strains seem limited to the ADS enzymes; 11 other enzymes with primarily metabolic functions show no obvious effect of selection on their activity levels whereas six other enzymes postulated to play a role in flux control may actually be involved in NADPH reoxidation and thus support the enhanced activities of the ADS enzymes. Thus, alterations in the longevity of these Drosophila strains are directly correlated with corresponding alterations in; 1) the mRNA levels of certain antioxidant defense system genes; 2) the protein level of at least one antioxidant defense system gene; 3) the activity levels of the corresponding antioxidant defense system enzymes, and 4) the ability of the organism to resist the biological damage arising from oxidative stress.

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Year:  2000        PMID: 10767577     DOI: 10.1016/s0531-5565(99)00094-7

Source DB:  PubMed          Journal:  Exp Gerontol        ISSN: 0531-5565            Impact factor:   4.032


  21 in total

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Journal:  Genetics       Date:  2004-12       Impact factor: 4.562

3.  Metabolic alterations in genetically selected Drosophila strains with different longevities.

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Review 4.  Antioxidant vitamins and mineral supplementation, life span expansion and cancer incidence: a critical commentary.

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5.  Effects of Different Levels of Dietary Zinc-Threonine and Zinc Oxide on the Zinc Bioavailability, Biological Characteristics and Performance of Honey Bees (Apis mellifera L.).

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6.  Mitochondrial ROS production correlates with, but does not directly regulate lifespan in Drosophila.

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7.  Induced overexpression of mitochondrial Mn-superoxide dismutase extends the life span of adult Drosophila melanogaster.

Authors:  Jingtao Sun; Donna Folk; Timothy J Bradley; John Tower
Journal:  Genetics       Date:  2002-06       Impact factor: 4.562

8.  Drosophila selected for extended longevity are more sensitive to heat shock.

Authors:  K Kuether; R Arking
Journal:  Age (Omaha)       Date:  1999-10

Review 9.  What have two decades of laboratory life-history evolution studies on Drosophila melanogaster taught us?

Authors:  N G Prasad; Amitabh Joshi
Journal:  J Genet       Date:  2003 Apr-Aug       Impact factor: 1.166

10.  Honey bee (Apis mellifera) drones survive oxidative stress due to increased tolerance instead of avoidance or repair of oxidative damage.

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Journal:  Exp Gerontol       Date:  2016-07-12       Impact factor: 4.032

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