Article abstract
Nature Genetics 39, 476 - 485 (2007)
Published online: 18 March 2007 | doi:10.1038/ng2004
Life extension through neurofibromin mitochondrial regulation and antioxidant therapy for neurofibromatosis-1 in Drosophila melanogaster
James Jiayuan Tong1,2, Samuel E Schriner1, David McCleary1, Brian J Day3 & Douglas C Wallace1
Abstract
We investigated the pathophysiology of neurofibromatosis-1 (NF1) in Drosophila melanogaster by inactivation or overexpression of the NF1 gene. NF1 gene mutants had shortened life spans and increased vulnerability to heat and oxidative stress in association with reduced mitochondrial respiration and elevated reactive oxygen species (ROS) production. Flies overexpressing NF1 had increased life spans, improved reproductive fitness, increased resistance to oxidative and heat stress in association with increased mitochondrial respiration and a 60% reduction in ROS production. These phenotypic effects proved to be modulated by the adenylyl cyclase/cyclic AMP (cAMP)/protein kinase A pathway, not the Ras/Raf pathway. Treatment of wild-type D. melanogaster with cAMP analogs increased their life span, and treatment of NF1 mutants with metalloporphyrin catalytic antioxidant compounds restored their life span. Thus, neurofibromin regulates longevity and stress resistance through cAMP regulation of mitochondrial respiration and ROS production, and NF1 may be treatable using catalytic antioxidants.
- Center for Molecular and Mitochondrial Medicine and Genetics with Departments of Biological Chemistry, Ecology and Evolutionary Biology and Pediatrics University of California, Irvine, California 92697, USA.
- Multidisciplinary Exercise Program, Biophysics and Physiology, University of California, Irvine, California 92697, USA.
- National Jewish Medical Research Center, Denver, Colorado 80206, USA.
Correspondence to: Douglas C Wallace1 e-mail: dwallace@uci.edu
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