Thioredoxin Peroxidases, Oxidative Stress, and Aging
Project Number5R01AG020715-04
Contact PI/Project LeaderORR, WILLIAM C.
Awardee OrganizationSOUTHERN METHODIST UNIVERSITY
Description
Abstract Text
DESCRIPTION: (provided by applicant) The thioredoxin peroxidases represent a
group of recently identified components of the antioxidative network, which
reduce H2O2 and organic peroxides using thioredoxin as an electron source.
These ubiquitous species are thought to play a particularly critical role in
insects, given the lack of glutathione peroxidase activity in these animals.
The purpose of the present study is to determine if the enhancement of
thioredoxin peroxidase activity would lower the level of oxidative stress,
thereby slowing the rate of the aging process, while a reduction in activity
would increase the level of oxidative stress and accelerate the rate of aging.
The specific focus of this study will be two distinct thioredoxin peroxidase
genes, which are expressed at high levels in the adult tissues of Drosophila
melanogaster. One of them has been localized to the mitochondria (DPx-5037),
while the other has been identified as a secreted form (DPx-4 156).
Reduction in thioredoxin peroxidase activity will be accomplished in Drosophila
by under-expression, through RNA interference and/or the through the use of
mutant alleles isolated by standard genetic approaches. Enhancement of
thioredoxin peroxidase activity will be accomplished by over-expression by
transgenic methodology, either using transgenes under control of the native
promoters or engineered to be inducible by antibiotic administration. The
effects of over- and under-expresssion of these genes on life span and a
variety of biochemical/physiological alterations related to the aging process
will be determined. Results should (i) provide a direct test of the role of the
thioredoxin peroxidases in the aging process, (ii) permit further assessment of
the validity of the oxidative stress hypothesis of aging, and (iii) aid in the
design of similar studies in mammals.
No Sub Projects information available for 5R01AG020715-04
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