Chapter 15 Cell differentiation as a response to oxidative stress

British Mycological Society Symposia Series

Volumn 27, Issue C, 2008, Pages 235-257

  Hansberg, Wilhelm ^a   Aguirre, Jesús ^a   Rís Momberg, Mauricio ^a   Rangel, Pablo ^a   Peraza, Leonardo ^a   Montes de Oca, Yésika ^a   Cano Domínguez, Nallely ^a  

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

EID: 48949105781     PISSN: 02750287     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S0275-0287(08)80057-4     Document Type: Article

References (54)

1. Accorsi K., Giglione C., Vanoni M., and Parmeggiani A. The Ras GDP/GTP cycle is regulated by oxidizing agents at the level of Ras regulators and effectors. FEBS Letters 492 (2001) 139-145
2. Aguirre J., and Hansberg W. Oxidation of Neurospora crassa glutamine synthetase. Journal of Bacteriology 166 (1986) 1040-1045
3. Aguirre J., Ríos-Momberg M., Hewitt D., and Hansberg W. Reactive oxygen species and development in microbial eukaryotes. Trends in Microbiology 13 (2005) 111-118
4. Aguirre J., Rodríguez R., and Hansberg W. Oxidation of Neurospora crassa NADP-specific glutamate dehydrogenase by activated oxygen species. Journal of Bacteriology 171 (1989) 6243-6250
5. Belden W.J., Larrondo L.F., Froehlich A.C., Shi M., Chen C.H., Loros J.J., and Dunlap J.C. The band mutation in Neurospora crassa is dominant allele of ras-1 implicating RAS signaling in circadian output. Genes & Development 21 (2007) 1494-1505
6. Blokhina O., Virolainen E., and Fagerstedt K.V. Antioxidants, oxidative damage and oxygen deprivation stress: A review. Annals of Botany 91 (2003) 179-194
7. Burdon R.H. Superoxide, hydrogen peroxide in relation to mammalian cell proliferation. Free Radical Biology & Medicine 18 (1995) 775-794
8. Cambareri E.B., Jensen B.C., Schabtach E., and Selker E.U. Repeat-induced G-C to A-T mutations in Neurospora. Science 244 (1989) 1571-1575
9. Canfield D.E. The early history of atmospheric oxygen: Homage to Robert M. Garrels. Annual Review of Earth and Planetary Sciences 33 (2005) 1-36
10. Cárdenas M.E., and Hansberg W. Glutamine requirement for aerial mycelium growth in Neurospora crassa. Journal of General and Applied Microbiology 130 (1984) 1723-1732
11. Cárdenas M.E., and Hansberg W. Glutamine metabolism during aerial mycelium growth of Neurospora crassa. Journal of General and Applied Microbiology 130 (1984) 1733-1741
12. Chauhan N., Latge J.-P., and Calderone R. Signalling and oxidant adaptation in Candida albicans and Aspergillus fumigatus. Nature Reviews Microbiology 4 (2006) 435-444
13. Chen C., and Dickman M.B. Dominant active Rac and dominant negative Rac revert the dominant active Ras phenotype in Colletotrichum trifolii by distinct signalling pathways. Molecular Microbiology 51 (2004) 1493-1507
14. Daub M.E., and Ehrenshaft M. The photoactivated cercospora toxin cercosporin: Contributions to plant disease and fundamental biology. Annual Review of Phytopathology 38 (2000) 461-490
15. Droge W. Free radicals in the physiological control of cell function. Physiological Review 82 (2002) 47-95
16. Dunlap J.C. Molecular bases for circadian clocks. Cell 96 (1999) 271-290
17. Esposito F., Ammendola R., Faraonio R., Russo T., and Cimino F. Redox control of signal transduction, gene expression and cellular senescence. Neurochemical Research 29 (2004) 617-628
18. Fang F.C. Antimicrobial reactive oxygen and nitrogen species: concepts and controversies. Nature Reviews Microbiology 2 (2004) 820-832
19. Gapper C., and Dolan L. Control of plant development by reactive oxygen species. Plant Physiology 141 (2006) 341-345
20. Giaccia A.J., Simon M.C., and Johnson R. The biology of hypoxia: the role of oxygen sensing in development, normal function, and disease. Genes & Development 18 (2004) 2183-2194
21. Halliwell B., and Gutteridge J.M.C. Free Radicals in Biology and Medicine. 3rd edn (1999), Oxford University Press
22. Hansberg W. A hyperoxidant state at the start of each developmental stage during Neurospora crassa conidiation. Ciencia e Cultura 48 (1996) 68-74
23. Hansberg W., and Aguirre J. Hyperoxidant states cause microbial cell differentiation by cell isolation from dioxygen. Journal of Theoretical Biology 142 (1990) 201-221
24. Hansberg W., de Groot H., and Sies H. Reactive oxygen species associated with cell differentiation in Neurospora crassa. Free Radical Biology & Medicine 14 (1993) 287-293
25. Heo J., and Campbell S.L. Ras regulation by reactive oxygen and nitrogen species. Biochemistry 45 (2006) 2200-2210
26. Herve C., Tonon T., Collen J., Corre E., and Boyen C. NADPH oxidases in eukaryotes: Red algae provide new hints!. Current Genetics 49 (2006) 190-204
27. Hordijk P.L. Regulation of NADPH oxidases: The role of Rac proteins. Circulation Research 98 (2006) 453-462
28. Irani K., Xia Y., Zweier J.L., Sollott S.J., Der C.J., Fearon E.R., Sundaresan M., Finkel T., and Goldschmidt-Clermont P.J. Mitogenic signaling mediated by oxidants in Ras-transformed fibroblasts. Science 275 (1997) 1649-1652
29. Klotz M.G., and Loewen P.C. The molecular evolution of catalatic hydroperoxidases: Evidence for multiple lateral transfer of genes between prokaryota and from bacteria into eukaryota. Molecular Biology and Evolution 20 (2003) 1098-1112
30. Lambeth J.D. NOX enzymes and the biology of reactive oxygen. Nature Review Immunology 4 (2004) 181-189
31. Lander H.M., Ogiste J.S., Teng K.K., and Novogrodsky A. p21 ras as a common signaling target of reactive free radicals and cellular redox stress. The Journal of Biological Chemistry 270 (1995) 21195-21198
32. Lara-Ortiz T., Riveros-Rosas H., and Aguirre J. Reactive oxygen species generated by microbial NADPH oxidase NoxA regulate sexual development in Aspergillus nidulans. Molecular Microbiology 50 (2003) 1241-1255
33. Lardy B., Bof M., Aubry L., Paclet M.H., Morel F., Satre M., and Klein G. NADPH oxidase homologs are required for normal cell differentiation and morphogenesis in Dictyostelium discoideum. Biochimica et Biophysica Acta 1744 (2005) 199-212
34. Li J., Stouffs M., Serrander L., Banfi B., Bettiol E., Charnay Y., Steger K., Krause K.-H., and Jaconi M.E. The NADPH oxidase NOX4 drives cardiac differentiation: Role in regulating cardiac transcription factors and MAP kinase activation. Molecular Biology of the Cell 17 (2006) 3978-3988
35. Lledías F., Rangel P., and Hansberg W. Singlet oxygen is part of a hyperoxidant state generated during spore germination. Free Radical Biology & Medicine 26 (1999) 1396-1404
36. Malagnac F., Lalucque H., Lepere G., and Silar P. Two NADPH oxidase isoforms are required for sexual reproduction and ascospore germination in the filamentous fungus Podospora anserina. Fungal Genetics and Biology 41 (2004) 982-997
37. Martindale J.L., and Holbrook N.J. Cellular response to oxidative stress: Signaling for suicide and survival. Journal of Cellular Physiology 192 (2002) 1
38. Michán S., Lledias F., Baldwin J.D., Natvig D.O., and Hansberg W. Regulation and oxidation of two large monofunctional catalases. Free Radical Biology and Medicine 33 (2002) 521-532
39. Michá n S., Lledias F., and Hansberg W. Asexual development is increased in Neurospora crassa cat-3-null mutant strains. Eukaryotic Cell 2 (2003) 798-808
40. Peraza L., and Hansberg W. Neurospora crassa catalases, singlet oxygen and cell differentiation. Biological Chemistry 383 (2002) 569-575
41. Raymond J., and Segre D. The effect of oxygen on biochemical networks and the evolution of complex life. Science 311 (2006) 1764-1767
42. Salmeen A., Andersen J.N., Myers M.P., Meng T.-C., Hinks J.A., Tonks N.K., and Barford D. Redox regulation of protein tyrosine phosphatase 1B involves a sulphenyl-amide intermediate. Nature 423 (2003) 769-773
43. Simon H.U., Haj-Yehia A., and Levi-Schaffer F. Role of reactive oxygen species (ROS) in apoptosis induction. Apoptosis 5 (2000) 415-418
44. Springer M.L., and Yanofsky C. A morphological and genetic analysis of conidiophore development in Neurospora crassa. Genes & Development 3 (1989) 559-571
45. Sugisaki S., Ito M., Toh-e A., Matsui Y., and Inoue H. Mutational analysis of the ras gene in Neurospora crassa. Fungal Genetics Conference (1999) 20 Abstract 368
46. Sundaresan M., Yu Z.-X., Ferrans V.J., Sulciner D.J., Gutkind J.S., Irani K., Goldschmidt-Clermont P.J., and Finkel T. Regulation of reactive-oxygen-species generation in fibroblasts by Rac1. The Biochemical Journal 318 (1996) 379-382
47. Tanaka A., Christensen M.J., Takemoto D., Park P., and Scott B. Reactive oxygen species play a role in regulating a fungus-perennial ryegrass mutualistic interaction. The Plant Cell 18 (2006) 1052-1066
48. Toledo I., Aguirre J., and Hansberg W. Aerial growth in Neurospora crassa: Characterization of an experimental model system. Experimental Mycology 10 (1986) 114-125
49. Toledo I., Aguirre J., and Hansberg W. Enzyme inactivation related to a hyperoxidant state during conidiation of Neurospora crassa. Microbiology 140 (1994) 2391-2397
50. Toledo I., and Hansberg W. Protein oxidation related to morphogenesis in Neurospora crassa. Experimental Mycology 14 (1990) 184-189
51. Toledo I., Noronha-Dutra A.A., and Hansberg W. Loss of NAD(P)-reducing power and glutathione disulfide excretion at the start of induction of aerial growth in Neurospora crassa. Journal of Bacteriology 173 (1991) 3243-3249
52. Toledo I., Rangel P., and Hansberg W. Redox imbalance at the start of each morphogenetic step of Neurospora crassa conidiation. Archives of Biochemistry and Biophysics 319 (1995) 519-524
53. Torres M., and Forman H.J. Redox signaling and the MAP kinase pathways. Biofactors 17 (2003) 287-296
54. Welinder K.G. Bacterial catalase-peroxidases are gene duplicated members of the plant peroxidase superfamily. Biochemica et Biophysica Acta 1080 (1991) 215-220