Life span and stress resistance of Caenorhabditis elegans are differentially affected by glutathione transferases metabolizing 4-hydroxynon-2-enal

Mechanisms of Ageing and Development

Volumn 128, Issue 2, 2007, Pages 196-205

  Ayyadevara, Srinivas ^a,b   Dandapat, Abhijit ^a   Singh, Sharda P ^a   Siegel, Eric R ^a   Shmookler Reis, Robert J ^a,b,c   Zimniak, Ludwika ^a   Zimniak, Piotr ^a,c  

^a UNIVERSITY OF ARKANSAS FOR MEDICAL SCIENCES   (United States)

^b UNIVERSITY OF ARKANSAS FOR MEDICAL SCIENCES   (United States)

^c CENTRAL ARKANSAS VETERANS HEALTHCARE SYSTEM   (United States)

Author keywords

4 HNE; 4 Hydroxynonenal; Aging; Caenorhabditis elegans; Glutathione transferase (GST); Longevity

Indexed keywords

4 HYDROXYNONENAL; GLUTATHIONE TRANSFERASE;

AGING; ARTICLE; CAENORHABDITIS ELEGANS; CATALYSIS; CONTROLLED STUDY; ELECTROPHILIC STRESS; GENE EXPRESSION; LIFESPAN; LIPID PEROXIDATION; LONGEVITY; NEMATODE; NONHUMAN; OXIDATIVE STRESS; PRIORITY JOURNAL; PROTEIN FUNCTION; RNA INTERFERENCE; STRESS; TISSUE SPECIFICITY;

ALDEHYDES; ANIMALS; CAENORHABDITIS ELEGANS; CAENORHABDITIS ELEGANS PROTEINS; GLUTATHIONE TRANSFERASE; LONGEVITY; RNA INTERFERENCE; STRESS, PSYCHOLOGICAL;

CAENORHABDITIS ELEGANS;

EID: 33846206430     PISSN: 00476374     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.mad.2006.11.025     Document Type: Article

References (43)

1. Alcedo J., and Kenyon C. Regulation of C. elegans longevity by specific gustatory and olfactory neurons. Neuron 41 (2004) 45-55
2. Alin P., Danielson U.H., and Mannervik B. 4-Hydroxyalk-2-enals are substrates for glutathione transferase. FEBS Lett. 179 (1985) 267-270
3. Ayyadevara S., Dandapat A., Singh S.P., Benes H., Zimniak L., Shmookler Reis R.J., and Zimniak P. Lifespan extension in hypomorphic daf-2 mutants of Caenorhabditis elegans is partially mediated by glutathione transferase CeGSTP2-2. Aging Cell 4 (2005) 299-307
4. Ayyadevara S., Engle M.R., Singh S.P., Dandapat A., Lichti C.F., Benes H., Shmookler Reis R.J., Liebau E., and Zimniak P. Lifespan and stress resistance of Caenorhabditis elegans are increased by expression of glutathione transferases capable of metabolizing the lipid peroxidation product 4-hydroxynonenal. Aging Cell 4 (2005) 257-271
5. Bagley A.C., Krall J., and Lynch R.E. Superoxide mediates the toxicity of paraquat for Chinese hamster ovary cells. Proc. Natl. Acad. Sci. U.S.A. 83 (1986) 3189-3193
6. Bianchi L., Kwok S.M., Driscoll M., and Sesti F. A potassium channel-MiRP complex controls neurosensory function in Caenorhabditis elegans. J. Biol. Chem. 278 (2003) 12415-12424
7. Birmingham A., Anderson E.M., Reynolds A., Ilsley-Tyree D., Leake D., Fedorov Y., Baskerville S., Maksimova E., Robinson K., Karpilow J., Marshall W.S., and Khvorova A. 3′ UTR seed matches, but not overall identity, are associated with RNAi off-targets. Nat. Methods 3 (2006) 199-204
8. Brenner S. The genetics of Caenorhabditis elegans. Genetics 77 (1974) 71-94
9. Carbone D.L., Doorn J.A., and Petersen D.R. 4-Hydroxynonenal regulates 26S proteasomal degradation of alcohol dehydrogenase. Free Radic. Biol. Med. 37 (2004) 1430-1439
10. 3H) 4-hydroxy-2-trans-nonenal. Lipids 32 (1997) 779-782
11. Engle M.R., Singh S.P., Nanduri B., Ji X., and Zimniak P. Invertebrate glutathione transferases conjugating 4-hydroxynonenal: CeGST 5.4 from Caenorhabditis elegans. Chem. Biol. Interact. 133 (2001) 244-248
12. Gems D., and McElwee J.J. Broad spectrum detoxification: the major longevity assurance process regulated by insulin/IGF-1 signaling?. Mech. Ageing Dev. 126 (2005) 381-387
13. Gree R., Tourbah H., and Carrie R. Fumaraldehyde monodimethyl acetal: an easily accessible and versatile intermediate. Tetrahedron Lett. 27 (1986) 4983-4986
14. Harman D. Aging: a theory based on free radical and radiation chemistry. J. Gerontol. 11 (1956) 298-300
15. Holm S. A simple sequentially rejective multiple test procedure. Scand. J. Stat. 6 (1979) 65-70
16. Holt R.A., Subramanian G.M., Halpern A., Sutton G.G., Charlab R., Nusskern D.R., Wincker P., Clark A.G., Ribeiro J.M., Wides R., Salzberg S.L., Loftus B., Yandell M., Majoros W.H., Rusch D.B., Lai Z., Kraft C.L., Abril J.F., Anthouard V., Arensburger P., Atkinson P.W., Baden H., de Berardinis V., Baldwin D., Benes V., Biedler J., Blass C., Bolanos R., Boscus D., Barnstead M., Cai S., Center A., Chaturverdi K., Christophides G.K., Chrystal M.A., Clamp M., Cravchik A., Curwen V., Dana A., Delcher A., Dew I., Evans C.A., Flanigan M., Grundschober-Freimoser A., Friedli L., Gu Z., Guan P., Guigo R., Hillenmeyer M.E., Hladun S.L., Hogan J.R., Hong Y.S., Hoover J., Jaillon O., Ke Z., Kodira C., Kokoza E., Koutsos A., Letunic I., Levitsky A., Liang Y., Lin J.J., Lobo N.F., Lopez J.R., Malek J.A., McIntosh T.C., Meister S., Miller J., Mobarry C., Mongin E., Murphy S.D., O'Brochta D.A., Pfannkoch C., Qi R., Regier M.A., Remington K., Shao H., Sharakhova M.V., Sitter C.D., Shetty J., Smith T.J., Strong R., Sun J., Thomasova D., Ton L.Q., Topalis P., Tu Z., Unger M.F., Walenz B., Wang A., Wang J., Wang M., Wang X., Woodford K.J., Wortman J.R., Wu M., Yao A., Zdobnov E.M., Zhang H., Zhao Q., Zhao S., Zhu S.C., Zhimulev I., Coluzzi M., della Torre A., Roth C.W., Louis C., Kalush F., Mural R.J., Myers E.W., Adams M.D., Smith H.O., Broder S., Gardner M.J., Fraser C.M., Birney E., Bork P., Brey P.T., Venter J.C., Weissenbach J., Kafatos F.C., Collins F.H., and Hoffman S.L. The genome sequence of the malaria mosquito Anopheles gambiae. Science 298 (2002) 129-149
17. Kaletta T., and Hengartner M.O. Finding function in novel targets: C. elegans as a model organism. Nat. Rev. Drug Discov. 5 (2006) 387-399
18. Kamath R.S., and Ahringer J. Genome-wide RNAi screening in Caenorhabditis elegans. Methods 30 (2003) 313-321
19. Kamath R.S., Fraser A.G., Dong Y., Poulin G., Durbin R., Gotta M., Kanapin A., Le Bot N., Moreno S., Sohrmann M., Welchman D.P., Zipperlen P., and Ahringer J. Systematic functional analysis of the Caenorhabditis elegans genome using RNAi. Nature 421 (2003) 231-237
20. Kimura H., Liu S., Yamada S., Uchida K., Matsumoto K., Mukaida M., and Yoshida K. Rapid increase in serum lipid peroxide 4-hydroxynonenal (HNE) through monocyte NADPH oxidase in early endo-toxemia. Free Radic. Res. 39 (2005) 845-851
21. Lanjuin A., and Sengupta P. Specification of chemosensory neuron subtype identities in Caenorhabditis elegans. Curr. Opin. Neurobiol. 14 (2004) 22-30
22. Leiers B.R., Kampkotter A., Grevelding C.G., Link C.D., Johnson T.E., and Henkle-Duhrsen K. A stress-responsive glutathione S-transferase confers resistance to oxidative stress in Caenorhabditis elegans. Free Radic. Biol. Med. 34 (2003) 1405-1415
23. McElwee J.J., Schuster E., Blanc E., Thomas J.H., and Gems D. Shared transcriptional signature in Caenorhabditis elegans dauer larvae and long-lived daf-2 mutants implicates detoxification system in longevity assurance. J. Biol. Chem. 279 (2004) 44533-44543
24. McEwen J.E., Zimniak P., Mehta J.L., and Shmookler Reis R.J. Molecular pathology of aging and its implications for senescent coronary atherosclerosis. Curr. Opin. Cardiol. 20 (2005) 399-406
25. Olsen G.J., Matsuda H., Hagstrom R., and Overbeek R. fastDNAmL: a tool for construction of phylogenetic trees of DNA sequences using maximum likelihood. Comput. Appl. Biosci. 10 (1994) 41-48
26. Page R.D.M. TreeView: an application to display phylogenetic trees on personal computers. Comput. Appl. Biosci. 12 (1996) 357-358
27. Pearl R. The Rate of Living (1928), University of London Press, London
28. Qiu S., Adema C.M., and Lane T. A computational study of off-target effects of RNA interference. Nucl. Acids Res. 33 (2005) 1834-1847
29. Ryazanov A.G., and Nefsky B.S. Protein turnover plays a key role in aging. Mech. Ageing Dev. 123 (2002) 207-213
30. Samara C., and Tavernarakis N. Calcium-dependent and aspartyl proteases in neurodegeneration and ageing in C. elegans. Ageing Res. Rev. 2 (2003) 451-471
31. Satoh K., Yamada S., Koike Y., Igarashi Y., Toyokuni S., Kumano T., Takahata T., Hayakari M., Tsuchida S., and Uchida K. A 1-hour enzyme-linked immunosorbent assay for quantitation of acrolein- and hydroxynonenal-modified proteins by epitope-bound casein matrix method. Anal. Biochem. 270 (1999) 323-328
32. Sawicki R., Singh S.P., Mondal A.K., Benes H., and Zimniak P. Cloning, expression, and biochemical characterization of one Epsilon-class (GST-3) and ten Delta-class (GST-1) glutathione S-transferases from Drosophila melanogaster, and identification of additional nine members of the Epsilon class. Biochem. J. 370 (2003) 661-669
33. Selley M.L., Bartlett M.R., McGuiness J.A., Hapel A.J., Ardlie N.G., and Lacey M.J. Determination of the lipid peroxidation product trans-4-hydroxy-2-nonenal in biological samples by high-performance liquid chromatography and combined capillary column gas chromatography-negative-ion chemical ionisation mass spectrometry. J. Chromatogr. 488 (1989) 329-340
34. Shmookler Reis R.J. Toward a unified theory of aging-what mammals can learn from worms and other ephemeral creatures. In: Cutler R.G., and Rodriguez H. (Eds). Oxidative Stress and Aging: Advances in Basic Science, Diagnostics and Intervention vol. 2 (2003), World Scientific Publishing, Singapore 1263-1283
35. Simmer F., Tijsterman M., Parrish S., Koushika S.P., Nonet M.L., Fire A., Ahringer J., and Plasterk R.H. Loss of the putative RNA-directed RNA polymerase RRF-3 makes C. elegans hypersensitive to RNAi. Curr. Biol. 12 (2002) 1317-1319
36. Singh S.P., Coronella J.A., Beneš H., Cochrane B.J., and Zimniak P. Catalytic function of Drosophila melanogaster glutathione S-transferase DmGSTS1-1 (GST-2) in conjugation of lipid peroxidation end products. Eur. J. Biochem. 268 (2001) 2912-2923
37. Spies-Martin D., Sommerburg O., Langhans C.D., and Leichsenring M. Measurement of 4-hydroxynonenal in small volume blood plasma samples: modification of a gas chromatographic-mass spectrometric method for clinical settings. J. Chromatogr. B 774 (2002) 231-239
38. Strohmaier H., Hinghofer-Szalkay H., and Schaur R.J. Detection of 4-hydroxynonenal (HNE) as a physiological component in human plasma. J. Lipid Mediators Cell Signal. 11 (1995) 51-61
39. Tavernarakis N., and Driscoll M. Caloric restriction and lifespan: a role for protein turnover?. Mech. Ageing Dev. 123 (2002) 215-229
40. Tavernarakis N., Wang S.L., Dorovkov M., Ryazanov A., and Driscoll M. Heritable and inducible genetic interference by double-stranded RNA encoded by transgenes. Nat. Genet. 24 (2000) 180-183
41. Tsuchiya Y., Yamaguchi M., Chikuma T., and Hojo H. Degradation of glyceraldehyde-3-phosphate dehydrogenase triggered by 4-hydroxy-2-nonenal and 4-hydroxy-2-hexenal. Arch. Biochem. Biophys. 438 (2005) 217-222
42. Uchida K. 4-Hydroxy-2-nonenal: a product and mediator of oxidative stress. Prog. Lipid Res. 42 (2003) 318-343
43. Zhang H., Dickinson D.A., Liu R.M., and Forman H.J. 4-Hydroxynonenal increases γ-glutamyl transpeptidase gene expression through mitogen-activated protein kinase pathways. Free Radic. Biol. Med. 38 (2005) 463-471