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Abstract:
In vitro studies have indicated that reactive oxygen species(ROS) and the oxidation of signaling molecules are importantmediators of signal transduction. We have identified two pathwaysby which the altered redox chemistry of the clk-1 mutants ofCaenorhabditis elegans acts in vivo on germline development.One pathway depends on the oxidation of an analog of vertebratelow density lipoprotein (LDL) and acts on the germline throughthe Ack-related tyrosine kinase (ARK-1) kinase and inositoltrisphosphate (IP3) signaling. The other pathway is the oncogenicras signaling pathway, whose action on germline as well as vulvaldevelopment appears to be modulated by cytoplasmic ROS.
Department of Biology, McGill University, 1205 Avenue Docteur Penfield, Montréal, Québec, Canada, H3A 1B1.
Decreased Energy Metabolism Extends Life Span in Caenorhabditis elegans Without Reducing Oxidative Damage.
J. M. Van Raamsdonk, Y. Meng, D. Camp, W. Yang, X. Jia, C. Benard, and S. Hekimi (2010)
Genetics
185, 559-571
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Label-free quantitative analysis of lipid metabolism in living Caenorhabditis elegans.
T. T. Le, H. M. Duren, M. N. Slipchenko, C.-D. Hu, and J.-X. Cheng (2010)
J. Lipid Res.
51, 672-677
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Evolutionary conservation of drug action on lipoprotein metabolism-related targets.
A. K. Hihi, M.-C. Beauchamp, R. Branicky, A. Desjardins, I. Casanova, M.-P. Guimond, M. Carroll, M. Ethier, I. Kianicka, K. McBride, et al. (2008)
J. Lipid Res.
49, 74-83
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A Measurable Increase in Oxidative Damage Due to Reduction in Superoxide Detoxification Fails to Shorten the Life Span of Long-Lived Mitochondrial Mutants of Caenorhabditis elegans.
Evolutionary conservation of the clk-1-dependent mechanism of longevity: loss of mclk1 increases cellular fitness and lifespan in mice.
X. Liu, N. Jiang, B. Hughes, E. Bigras, E. Shoubridge, and S. Hekimi (2005)
Genes & Dev.
19, 2424-2434
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Inactivation of Drosophila DJ-1 leads to impairments of oxidative stress response and phosphatidylinositol 3-kinase/Akt signaling.
Y. Yang, S. Gehrke, Md. E. Haque, Y. Imai, J. Kosek, L. Yang, M. F. Beal, I. Nishimura, K. Wakamatsu, S. Ito, et al. (2005)
PNAS
102, 13670-13675
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A crucial role for reactive oxygen species in RANKL-induced osteoclast differentiation.
N. K. Lee, Y. G. Choi, J. Y. Baik, S. Y. Han, D.-w. Jeong, Y. S. Bae, N. Kim, and S. Y. Lee (2005)
Blood
106, 852-859
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Microsomal Triglyceride Transfer Protein Promotes the Secretion of Xenopus laevis Vitellogenin A1.
J. A. Sellers, L. Hou, D. R. Schoenberg, S. R. Batistuzzo de Medeiros, W. Wahli, and G. S. Shelness (2005)
J. Biol. Chem.
280, 13902-13905
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Changes in Nuclear Receptor and Vitellogenin Gene Expression in Response to Steroids and Heavy Metal in Caenorhabditis elegans.
A. Novillo, S.-J. Won, C. Li, and I. P. Callard (2005)
Integr. Comp. Biol.
45, 61-71
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Demethoxy-Q, An Intermediate of Coenzyme Q Biosynthesis, Fails to Support Respiration in Saccharomyces cerevisiae and Lacks Antioxidant Activity.
S. Padilla, T. Jonassen, M. A. Jimenez-Hidalgo, D. J. M. Fernandez-Ayala, G. Lopez-Lluch, B. Marbois, P. Navas, C. F. Clarke, and C. Santos-Ocana (2004)
J. Biol. Chem.
279, 25995-26004
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Lack of Peroxisomal Catalase Causes a Progeric Phenotype in Caenorhabditis elegans.