Mitochondrial redox biology and homeostasis in plants

Trends in Plant Science

Volumn 12, Issue 3, 2007, Pages 125-134

  Noctor, Graham ^a   De Paepe, Rosine ^a   Foyer, Christine H ^b  

^a INSTITUTE OF PLANT SCIENCES PARIS SACLAY IPS2   (France)

^b NEWCASTLE UNIVERSITY   (United Kingdom)

Author keywords

[No Author keywords available]

Indexed keywords

NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; REACTIVE OXYGEN METABOLITE;

APOPTOSIS; CELL AGING; CYTOLOGY; ENERGY METABOLISM; GENETIC TRANSFORMATION; GENETICS; HOMEOSTASIS; METABOLISM; MITOCHONDRION; OXIDATION REDUCTION REACTION; PLANT; REVIEW; SIGNAL TRANSDUCTION;

APOPTOSIS; CELL AGING; ENERGY METABOLISM; HOMEOSTASIS; MITOCHONDRIA; NADP; OXIDATION-REDUCTION; PLANTS; REACTIVE OXYGEN SPECIES; SIGNAL TRANSDUCTION; TRANSFORMATION, GENETIC;

ANIMALIA;

EID: 33847613456     PISSN: 13601385     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tplants.2007.01.005     Document Type: Review

References (105)

1. Douce R., and Neuburger M. The uniqueness of plant mitochondria. Annu. Rev. Plant Physiol. Plant Mol. Biol. 40 (1989) 371-414
2. Møller I.M. Plant mitochondria and oxidative stress: electron transport, NADPH turnover, and metabolism of reactive oxygen species. Annu. Rev. Plant Physiol. Plant Mol. Biol. 52 (2001) 561-591
3. Hoefnagel M.H.N., et al. Interdependence between chloroplasts and mitochondria in the light and the dark. Biochim. Biophys. Acta 1366 (1998) 235-255
4. Raghavendra A.S., and Padmasree K. Beneficial interactions of mitochondrial metabolism with photosynthetic carbon assimilation. Trends Plant Sci. 8 (2003) 546-553
5. Rasmusson A.G., et al. Alternative NAD(P)H dehydrogenases of plant mitochondria. Annu. Rev. Plant Biol. 55 (2004) 23-39
6. Fernie A.R., et al. Respiratory metabolism: glycolysis, the TCA cycle and mitochondrial electron transport. Curr. Opin. Plant Biol. 7 (2004) 254-261
7. Ruuska S.A., et al. The capacity of green oil seeds to utilize photosynthesis to drive biosynthetic processes. Plant Physiol. 136 (2004) 2700-2709
8. Geigenberger P. Regulation of sucrose to starch conversion in growing potato tubers. J. Exp. Bot. 54 (2003) 457-465
9. Rhoads D.M., et al. Mitochondrial reactive oxygen species. Contribution to oxidative stress and interorganellar signaling. Plant Physiol. 141 (2006) 357-366
10. Noctor G., and Foyer C.H. Homeostasis of adenylate status during photosynthesis in a fluctuating environment. J. Exp. Bot. 51 (2000) 347-356
11. Atkin O.K., et al. The hot and the cold: unraveling the variable response of plant respiration to temperature. Funct. Plant Biol. 32 (2005) 87-105
12. Ishizaki K., et al. The critical role of Arabidopsis electron transfer flavoprotein:ubiquinone oxidoreductase during dark-induced starvation. Plant Cell 17 (2005) 2587-2600
13. Hanning I., and Heldt H.W. On the function of mitochondrial metabolism during photosynthesis in spinach (Spinacia oleracea L.) leaves. Plant Physiol. 103 (1993) 1147-1154
14. Bouché N., et al. Mitochondrial succinic-semialdehyde dehydrogenase of the γ-aminobutyrate shunt is required to restrict levels of reactive oxygen intermediates in plants. Proc. Natl. Acad. Sci. U. S. A. 100 (2003) 6843-6848
15. Dudkina N.V., et al. Respiratory chain supercomplexes in the plant mitochondrial membrane. Trends Plant Sci. 11 (2006) 232-240
16. + ratio provides evidence of a mitochondrial glycerol-3-phosphate shuttle in Arabidopsis. Plant Cell 18 (2006) 422-441
17. Bartoli C.G., et al. Ascorbate biosynthesis in mitochondria is linked to the electron transport chain between complexes III and IV. Plant Physiol. 123 (2000) 335-343
18. Clifton R., et al. Alternative oxidases in Arabidopsis: a comparative analysis of differential expression in the gene family provides new insights into function of non-phosphorylating bypasses. Biochim. Biophys. Acta 1757 (2006) 730-741
19. Vanlerberghe G.C., et al. In organello and in vivo evidence of the importance of the regulatory sulfhydryl/disulfide system and pyruvate for alternative oxidase activity in tobacco. Plant Physiol. 121 (1999) 793-803
20. Gelhaye E., et al. A specific form of thioredoxin h occurs in plant mitochondria and regulates the alternative oxidase. Proc. Natl. Acad. Sci. U. S. A. 101 (2004) 14545-14550
21. Umbach A.L., et al. Characterization of transformed Arabidopsis with altered alternative oxidase levels and analysis of effects on reactive oxygen species in tissue. Plant Physiol. 139 (2005) 1806-1820
22. Trono D., et al. The uncoupling protein and the potassium channel are activated by hyperosmotic stress in mitochondria from durum wheat seedlings. Plant Cell Environ. 27 (2004) 437-448
23. Purvis A.C. Role of the alternative oxidase in limiting superoxide production by plant mitochondria. Physiol. Plant. 100 (1997) 165-170
24. Maxwell D.P., et al. The alternative oxidase lowers mitochondrial reactive oxygen production in plant cells. Proc. Natl. Acad. Sci. U. S. A. 96 (1999) 8271-8276
25. Sweetlove L.J., et al. The impact of oxidative stress on Arabidopsis mitochondria. Plant J. 32 (2002) 891-904
26. Sweetlove L., and Foyer C.H. Roles for reactive oxygen species and antioxidants in plant mitochondria. In: Day D.A., et al. (Ed). Plant Mitochondria: from Genome to Function. Advances in Photosynthesis and Respiration Vol. 17 (2004), Kluwer Academic Publishers 307-320
27. Kristensen B.K., et al. Identification of oxidised proteins in the matrix of rice leaf mitochondria by immunoprecipitation and two-dimensional liquid chromatography-tandem mass spectrometry. Phytochemistry 65 (2004) 1839-1851
28. Møller I.M., and Kristensen B.K. Protein oxidation in plant mitochondria detected as oxidized tryptophan. Free Radic. Biol. Med. 40 (2006) 430-435
29. Job C., et al. Patterns of protein oxidation in Arabidopsis seeds and during germination. Plant Physiol. 138 (2005) 790-802
30. Marín-Navarro J., and Moreno J. Cysteines 449 and 459 modulate the reduction-oxidation conformational changes of ribulose 1,5-bisphosphate carboxylase/oxygenase and the translocation of the enzyme to membranes during stress. Plant Cell Environ. 29 (2006) 898-908
31. Chew O., et al. Molecular definition of the ascorbate-glutathione cycle in Arabidopsis mitochondria reveals dual targeting of antioxidant defenses in plants. J. Biol. Chem. 278 (2003) 46869-46877
32. Watanabe N., et al. Dual targeting of spinach protoporphyrinogen oxidase II to mitochondria and chloroplasts by alternative use of two in-frame initiation codons. J. Biol. Chem. 276 (2001) 20474-20481
33. Taylor N.L., et al. Environmental stresses inhibit and stimulate different protein import pathways in plant mitochondria. FEBS Lett. 547 (2003) 125-130
34. Yao N., and Greenberg J.T. Arabidopsis ACCELERATED CELL DEATH2 modulates programmed cell death. Plant Cell 18 (2006) 397-411
35. Laloi C., et al. Identification and characterization of a mitochondrial thioredoxin system in plants. Proc. Natl. Acad. Sci. U. S. A. 98 (2001) 14144-14149
36. Balmer Y., et al. Thioredoxin links redox to the regulation of fundamental processes of plant mitochondria. Proc. Natl. Acad. Sci. U. S. A. 101 (2004) 2642-2647
37. Beer S.M., et al. Glutaredoxin 2 catalyzes the reversible oxidation and glutathionylation of mitochondrial membrane thiol proteins. J. Biol. Chem. 279 (2004) 47939-47951
38. Finkemeier I., et al. The mitochondrial type II peroxiredoxin F is essential for redox homeostasis and root growth of Arabidopsis thaliana under stress. J. Biol. Chem. 280 (2005) 12168-12180
39. Bykova N.V., et al. Two separate transhydrogenase activities are present in plant mitochondria. Biochem. Biophys. Res. Commun. 265 (1999) 106-111
40. +-linked substrates by pea leaf mitochondria. Physiol. Plant. 111 (2001) 448-456
41. Planchet E., et al. Nitric oxide emission from tobacco leaves and cell suspensions: rate limiting factors and evidence for the involvement of mitochondrial electron transport. Plant J. 41 (2005) 732-743
42. Delledonne M. NO news is good news for plants. Curr. Opin. Plant Biol. 8 (2005) 390-396
43. Logan D.C. The mitochondrial compartment. J. Exp. Bot. 57 (2006) 1225-1243
44. Haggie P.M., and Verkman A.S. Diffusion of tricarboxylic acid cycle enzymes in the mitochondrial matrix: evidence for restricted mobility of a multienzyme complex. J. Biol. Chem. 277 (2002) 40782-40788
45. +-linked dehydrogenases from plant mitochondria. Plant Physiol. 94 (1990) 189-193
46. Budde R.J.A., et al. Acetyl-coenzyme A can regulate activity of the mitochondrial pyruvate dehydrogenase complex in situ. Plant Physiol. 95 (1991) 131-136
47. Igamberdiev A.U., and Gardeström P. Regulation of NAD- and NADP-dependent isocitrate dehydrogenases by reduction levels of pyridine nucleotides in mitochondria and cytosol of pea leaves. Biochim. Biophys. Acta 1606 (2003) 117-125
48. Giegé P., et al. Enzymes of glycolysis are functionally associated with the mitochondrion in Arabidopsis cells. Plant Cell 15 (2003) 2140-2151
49. Picault N., et al. The growing family of mitochondrial carriers in Arabidopsis. Trends Plant Sci. 9 (2004) 138-146
50. 3 plants. J. Exp. Bot. 53 (2002) 581-590
51. Tcherkez G., et al. In vivo respiratory metabolism of illuminated leaves. Plant Physiol. 138 (2005) 1596-1606
52. Igamberdiev A.U., et al. Involvement of cyanide-resistant and rotenone-insensitive pathways of mitochondrial electron transport during oxidation of glycine in higher plants. FEBS Lett. 412 (1997) 265-269
53. Bari R., et al. A glycolate dehydrogenase in the mitochondria of Arabidopsis thaliana. J. Exp. Bot. 55 (2004) 623-630
54. Plaxton W.C., and Podesta F.E. The functional organization and control of plant respiration. Crit. Rev. Plant Sci. 25 (2006) 159-198
55. Hodges M. Enzyme redundancy and the importance of 2-oxoglutarate in plant ammonium assimilation. J. Exp. Bot. 53 (2002) 905-916
56. Dutilleul C., et al. Functional mitochondrial complex I is required for optimal photosynthetic performance in photorespiratory conditions and during transients. Plant Physiol. 131 (2003) 264-275
57. Dutilleul C., et al. Leaf mitochondria modulate whole cell redox homeostasis, set antioxidant capacity and determine stress resistance through altered signaling and diurnal regulation. Plant Cell 15 (2003) 1212-1226
58. Schönfeld C., et al. The nucleus-encoded protein MOC1 is essential for mitochondrial light acclimation in Chlamydomonas reinhardtii. J. Biol. Chem. 279 (2004) 50366-50374
59. Nunes-Nesi A., et al. Enhanced photosynthetic performance and growth as a consequence of decreasing mitochondrial malate dehydrogenase activity in transgenic tomato plants. Plant Physiol. 137 (2005) 611-622
60. Pesaresi P., et al. Nuclear photosynthetic gene expression is synergistically modulated by rates of protein synthesis in chloroplasts and mitochondria. Plant Cell 18 (2006) 970-991
61. Priault P., et al. The mitochondrial CMSII mutation of Nicotiana sylvestris impairs adjustment of photosynthetic carbon assimilation to higher growth irradiance. J. Exp. Bot. 57 (2006) 2075-2085
62. Rasmusson A.G., and Escobar M.A. Light and diurnal regulation of plant respiratory gene expression. Physiol. Plant. 129 (2007) 57-67
63. Okada S., and Brennicke A. Transcript levels in plant mitochondria show a tight homeostasis during day and night. Mol. Gen. Genomics 276 (2006) 71-78
64. Heineke D., et al. Metabolic response of potato plants to an antisense reduction of the P-protein of glycine decarboxylase. Planta 212 (2001) 880-887
65. Igamberdiev A.U., et al. The role of photorespiration in redox and energy balance of photosynthetic plant cells: a study with a barley mutant deficient in glycine decarboxylase. Plant Physiol. 111 (2001) 427-438
66. Karpova O.V., et al. Differential expression of alternative oxidase genes in maize mitochondrial mutants. Plant Cell 14 (2002) 3271-3284
67. 2 levels and alters mitochondrial physiology in Arabidopsis. J. Mol. Biol. 350 (2005) 263-277
68. Pineau B., et al. Targeting the NAD7 subunit to mitochondria restores a functional complex I and a wild-type phenotype in the Nicotiana sylvestris CMSII mutant lacking nad7. J. Biol. Chem. 280 (2005) 25994-26001
69. Sabar M., et al. Complex I impairment, respiratory compensations, and photosynthetic decrease in nuclear and mitochondrial male sterile mutants of Nicotiana sylvestris. Plant Physiol. 124 (2000) 1239-1249
70. Dutilleul C., et al. Mitochondria-driven changes in leaf NAD status exert a crucial influence on the control of nitrate assimilation and the integration of carbon and nitrogen metabolism. Plant Physiol. 139 (2005) 64-78
71. Escobar M.A., et al. Reorganization of the alternative pathways of the Arabidopsis respiratory chain by nitrogen supply: opposing effects of ammonium and nitrate. Plant J. 45 (2006) 775-788
72. Leister D. Genomics-based dissection of the cross-talk of chloroplasts with the nucleus and mitochondria in Arabidopsis. Gene 354 (2005) 110-116
73. Bartoli C.G., et al. Inter-relationships between light and respiration in the control of ascorbic acid synthesis and accumulation in Arabidopsis thaliana leaves. J. Exp. Bot. 57 (2006) 1621-1631
74. Vidal, G. et al. Lack of respiratory chain Complex I impairs AOX engagement and modulates redox signaling during elicitor-induced cell death in tobacco. Plant Cell (in press)
75. Guy R.D., and Vanlerberghe G.C. Partitioning of respiratory electrons in the dark in leaves of transgenic tobacco with modified levels of alternative oxidase. Physiol. Plant. 125 (2005) 171-180
76. Gray J.C., et al. Stromules: mobile protrusions and interconnections between plastids. Plant Biol. 3 (2001) 223-233
77. Waters M.T., et al. Stromule formation is dependent upon plastid size, plastid differentiation status and the density of plastids within the cell. Plant J. 39 (2004) 655-667
78. Burger G., et al. Mitochondrial genomes: anything goes. Trends Genet. 19 (2003) 709-716
79. Ameisen J.C. On the origin, evolution, and nature of programmed cell death: a timeline of four billion years. Cell Death Differ. 9 (2002) 367-393
80. Dimri G.P. What has senescence got to with cancer?. Cancer Cell 7 (2005) 505-512
81. Buchanan-Wollaston V., et al. The molecular analysis of leaf senescence - a genomics approach. Plant Biotechnol. J. 1 (2003) 3-22
82. Schriner S.E., et al. Extension of murine lifespan by overexpression of catalase targeted to mitochondria. Science 308 (2005) 1909-1911
83. Hochstrasser M. Ubiquitin-dependent protein degradation. Annu. Rev. Genet. 30 (1996) 405-439
84. Yao N., et al. The mitochondrion-an organelle commonly involved in programmed cell death in Arabidopsis thaliana. Plant J. 40 (2004) 596-610
85. Apel K., and Hirt H. Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu. Rev. Plant Biol. 55 (2004) 373-399
86. Maxwell D.P., et al. Evidence of mitochondrial involvement in the transduction of signals required for the induction of genes associated with pathogen attack and senescence. Plant J. 29 (2002) 269-279
87. Joo J.H., et al. Different signalling and cell death roles of heterotrimeric G protein a and b subunits in the Arabidopsis oxidative stress response to ozone. Plant Cell 17 (2005) 957-970
88. Gomez L.D., et al. Regulation of calcium signaling and gene expression by glutathione. J. Exp. Bot. 55 (2004) 1851-1859
89. Pavet V., et al. Ascorbic acid deficiency activates cell death and disease resistance responses in Arabidopsis. Plant Physiol. 139 (2005) 1291-1303
90. Dat J.F., et al. Changes in hydrogen peroxide homeostasis trigger an active cell death process in tobacco. Plant J. 33 (2003) 1-12
91. Matsumura H., et al. Overexpression of Bax inhibitor suppresses the fungal elicitor-induced cell death in rice (Oryza sativa L.) cells. Plant J. 33 (2003) 425-437
92. Chen S., and Dickman M.B. Bcl-2 family members localize to tobacco chloroplasts and inhibit programmed cell death induced by chloroplast-targeted herbicides. J. Exp. Bot. 55 (2004) 2617-2623
93. Vacca R.A., et al. Cytochrome c is released in a reactive oxygen species-dependent manner and is degraded via caspase-like proteases in tobacco bright-yellow 2 cells en route to heat shock-induced cell death. Plant Physiol. 141 (2006) 208-219
94. Selga T., et al. Death of mitochondria during programmed cell death of leaf mesophyll cells. Cell Biol. Int. 29 (2005) 1050-1056
95. Uren A.G., et al. Identification of paracaspases and metacaspases: two ancient families of caspase-like proteins, one of which plays a key role in MALT lymphoma. Mol. Cell 6 (2000) 961-967
96. Foyer C.H., and Noctor G. Oxidant and antioxidant signaling in plants: a re-evaluation of the concept of oxidative stress in a physiological context. Plant Cell Environ. 29 (2005) 1056-1071
97. Miller R.A. The anti-aging sweepstakes: catalase runs for the ROSes. Science 308 (2005) 1875-1876
98. Chen Q., et al. Production of reactive oxygen species by mitochondria. Central role of complex III. J. Biol. Chem. 278 (2003) 36027-36031
99. Foyer C.H., and Noctor G. Redox sensing and signalling associated with reactive oxygen in chloroplasts, peroxisomes and mitochondria. Physiol. Plant. 119 (2003) 355-364
100. Young T.A., et al. Reactive oxygen species production by the mitochondrial respiratory chain in isolated rat hepatocytes and liver mitochondria: studies using myxothiazol. Arch. Biochem. Biophys. 405 (2002) 65-72
101. Sorensen M., et al. Effects of fasting on oxidative stress in rat liver mitochondria. Free Radic. Res. 40 (2006) 339-347
102. Korshunov S.S., et al. High protonic potential actuates a mechanism of production of reactive oxygen species in mitochondria. FEBS Lett. 416 (1997) 15-18
103. Queval G., and Noctor G. A plate-reader method for the measurement of NAD, NADP, glutathione and ascorbate in tissue extracts. Application to redox profiling during Arabidopsis rosette development. Anal. Biochem. (2007) 10.1016/j.ab.2007.01.005
104. Kasimova M.R., et al. The free NADH concentration is kept constant in plant mitochondria under different metabolic conditions. Plant Cell 18 (2006) 688-698
105. Vanacker H., et al. A role for salicylic acid and NPR1 in regulating cell growth in Arabidopsis. Plant J. 28 (2001) 209-216