The work is reported in Current Biology by two independent groups, one led by Nancy Bonini of the University of Pennsylvania and the Howard Hughes Medical Institute, and the other led by Kyung-Tai Min of the NINDS branch of the U.S. National Institutes of Health.
Parkinson's disease occurs both sporadically and as a result of inheritance of single gene mutations. One of the most common neurodegenerative disorders, it is associated with the progressive and selective loss of a specific population of neurons in the brain, the dopaminergic neurons of the substantia nigra pars compacta . Exposure to several common environmental toxins, thought to injure neurons through oxidative damage, has been shown to be associated with sporadic forms of Parkinson's disease. During the past decade, researchers have also made remarkable progress in identifying genes responsible for inherited forms of Parkinson's disease, with the expectation that understanding the function of these genes will elucidate mechanisms behind sporadic Parkinson's disease. Past work had shown that one form of familial Parkinson's disease results from a loss of function of a gene called DJ-1.
The fruit fly possesses two versions of the DJ-1 gene, and in the new work, the researchers simulated the human Parkinson's disease situation by deleting one or both forms of DJ-1 from the fly's DNA.
Bonini and colleagues showed that flies lacking both forms of DJ-1 activity are normal under standard conditions. However, upon exposure to widely used agricultural agents, including paraquat and rotenone, previously associated with the sporadic form of Parkinson's disease, the flies show strikingly increased sensitivity and death. These findings suggest that loss of DJ-1 function leads to an increased sensitivity to chemical agents that cause oxidative damage.
Min and his colleagues found that loss of function of one form of fly DJ-1, DJ-1b, caused a compensatory boost in expression of the other form of the gene, DJ-1a. These flies, lacking DJ-1â function but having increased DJ-1á activity, showed extended survival of dopaminergic neurons and resistance to oxidative stress caused by the chemical paraquat, but at the same time they also exhibited acute sensitivity to hydrogen peroxide treatment. The results showed that overexpression of DJ-1a in dopaminergic neurons is sufficient to confer protection against paraquat insult.
Together, the results from the two studies suggest that Drosophila DJ-1 genes, and potentially human DJ-1, play critical roles in the survival of dopaminergic neurons and the response to oxidative cellular stress. In addition, the studies also highlight DJ-1 as a potential therapeutic target for the treatment of Parkinson's disease.
The researchers include Marc Meulener, Cecilia E. Armstrong-Gold and Nancy M. Bonini of the University of Pennsylvania in Philadelphia, PA; Alexander J. Whitworth and Leo J. Pallanck of the University of Washington School of Medicine in Seattle, WA; Patrizia Rizzu and Peter Heutink of the VU University Medical Center in Amsterdam, The Netherlands; and Paul D. Wes of Elan Pharmaceuticals in South San Francisco, CA. This work was supported by a neurodegeneration training grant from the University of Pennsylvania, the Measey Foundation, and a National Research Service Award (National Institute of Neurological Disorders and Stroke) (to M.M.), the NIA (to N.M.B.), and a grant from the National Institutes of Health (to L.J.P.).
Meulener et al.: "Drosophila DJ-1 mutants are selectively sensitive to environmental toxins associated with Parkinson's disease" Publishing in Current Biology, Vol. 15, pages 1572-1577, September 6, 2005. DOI 10.1016/j.cub.2005.07.064 www.current-biology.com