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2011 | 33 | 2 |

Tytuł artykułu

Isolation and characterization of Arabidopsis mutants with enhanced tolerance to oxidative stress

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
We have previously reported a method for isolation of mutants with enhanced tolerance to the fungal AAL toxin and given a detailed characterization of atr1 (AAL toxin resistant, Gechev et al. in Biochem Biophys Res Commun 375:639–644, 2008). Herewith, we report eight more mutants with enhanced tolerance to the AAL toxin. Phenotypic analysis showed that six of the mutants were reduced in size compared with their original background loh2. Furthermore, atr2 showed delayed flowering and senescence. The mutants were also evaluated for oxidative stress tolerance by growing them on ROS-inducing media supplemented with either aminotriazole or paraquat, generating, respectively, H₂O₂ or superoxide radicals. Oxidative stress, confirmed by induction of the marker genes, HIGH AFFINITY NITRATE TRANSPORTER At1G08090 and HEAT SHOCK PROTEIN 17 At3G46230, inhibited growth of all lines. However, while the original background loh2 developed necrotic lesions and died rapidly on ROS-inducing plant growth media, atr1, atr2, atr7 and atr9 remained green and viable. The tolerance against oxidative stress-induced cell death was confirmed by fresh weight and chlorophyll measurements. Real-time PCR analysis revealed that the expression of the EXTENSIN gene At5G46890, previously shown to be downregulated by aminotriazole in atr1, was repressed in all lines, consistent with the growth inhibition induced by oxidative stress. Taken together, the data indicate a complex link between growth, development and oxidative stress tolerance and indicates that growth inhibition can be uncoupled from oxidative stress-induced cell death.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

33

Numer

2

Opis fizyczny

p.375-382,fig.,ref.

Twórcy

autor
  • Department Molecular Biology of Plants, University of Groningen, Kerklaan 30, 9751 NN Haren, The Netherlands
autor
  • Department of Plant Physiology and Plant Molecular Biology, University of Plovdiv, 24 Tsar Assen str., 4000 Plovdiv, Bulgaria
autor
  • Department of Plant Physiology and Plant Molecular Biology, University of Plovdiv, 24 Tsar Assen str., 4000 Plovdiv, Bulgaria
autor
  • Department of Plant Physiology and Plant Molecular Biology, University of Plovdiv, 24 Tsar Assen str., 4000 Plovdiv, Bulgaria
autor
  • Department Molecular Biology of Plants, University of Groningen, Kerklaan 30, 9751 NN Haren, The Netherlands
autor
  • Department of Plant Physiology and Plant Molecular Biology, University of Plovdiv, 24 Tsar Assen str., 4000 Plovdiv, Bulgaria

Bibliografia

  • Apel K, Hirt H (2004) Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annu Rev Plant Biol 55:373–399
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  • Brandwagt BF, Mesbah LA, Takken FLW, Laurent PL, Kneppers TJA, Hille J, Nijkamp HJJ (2000) A longevity assurance gene homolog of tomato mediates resistance to Alternaria alternata f. sp lycopersici toxins and fumonisin B1. Proc Natl Acad Sci USA 97:4961–4966
  • Chen M, Markham JE, Dietrich CR, Jaworski JG, Cahoon EB (2008) Sphingolipid long-chain base hydroxylation is important for growth and regulation of sphingolipid content and composition in Arabidopsis. Plant Cell 20:1862–1878
  • Chen R, Sun S, Wang C, Li Y, Liang Y, An F, Li C, Dong H, Yang X, Zhang J, Zuo J (2009) The Arabidopsis PARAQUAT RESISTANT2 gene encodes an S-nitrosoglutathione reductase that is a key regulator of cell death. Cell Res 19:1377–1387
  • Dat JF, Pellinen R, Beeckman T, van de Cotte B, Langebartels C, Kangasjarvi J, Inzè D, Van Breusegem F (2003) Changes in hydrogen peroxide homeostasis trigger an active cell death process in tobacco. Plant J 33:621–632
  • Gadjev I, Stone JM, Gechev T (2008) Programmed cell death in plants: new insights into redox regulation and the role of hydrogen peroxide. Int Rev Cell Mol Biol 270:87–144
  • Gechev TS, Hille J (2005) Hydrogen peroxide as a signal controlling plant programmed cell death. J Cell Biol 168:17–20
  • Gechev T, Gadjev I, Van Breusegem F, Inzè D, Dukiandjiev S, Toneva V, Minkov I (2002) Hydrogen peroxide protects tobacco from oxidative stress by inducing a set of antioxidant enzymes. Cell Mol Life Sci 59:708–714
  • Gechev T, Willekens H, Van Montagu M, Inzè D, Van Camp W, Toneva V, Minkov I (2003) Different responses of tobacco antioxidant enzymes to light and chilling stress. J Plant Physiol 160:509–515
  • Gechev TS, Gadjev IZ, Hille J (2004) An extensive microarray analysis of AAL-toxin-induced cell death in Arabidopsis thaliana brings new insights into the complexity of programmed cell death in plants. Cell Mol Life Sci 61:1185–1197
  • Gechev TS, Minkov IN, Hille J (2005) Hydrogen peroxide-induced cell death in Arabidopsis: transcriptional and mutant analysis reveals a role of an oxoglutarate-dependent dioxygenase gene in the cell death process. IUBMB Life 57:181–188
  • Gechev TS, Van Breusegem F, Stone JM, Denev I, Laloi C (2006) Reactive oxygen species as signals that modulate plant stress responses and programmed cell death. Bioessays 28:1091–1101
  • Gechev T, Ferwerda M, Mehterov N, Laloi C, Qureshi MK, Hille J (2008) Arabidopsis AAL-toxin-resistant mutant atr1 shows enhanced tolerance to programmed cell death induced by reactive oxygen species. Biochem Biophys Res Commun 375:639–644
  • Op Den Camp RGL, Przybyla D, Ochsenbein C, Laloi C, Kim CH, Danon A, Wagner D, Hideg E, Gobel C, Feussner I, Nater M, Apel K (2003) Rapid induction of distinct stress responses after the release of singlet oxygen in Arabidopsis. Plant Cell 15:2320–2332
  • Shi LH, Bielawski J, Mu JY, Dong HL, Teng C, Zhang J, Yang XH, Tomishige N, Hanada K, Hannun YA, Zuo JR (2007) Involvement of sphingoid bases in mediating reactive oxygen intermediate production and programmed cell death in Arabidopsis. Cell Res 17:1030–1040
  • Spassieva SD, Markham JE, Hille J (2002) The plant disease resistance gene Asc-1 prevents disruption of sphingolipid metabolism during AAL-toxin-induced programmed cell death. Plant J 32:561–572
  • Teufel A, Maass T, Galle PR, Malik N (2009) The longevity assurance homologue of yeast lag1 (Lass) gene family. Int J Mol Med 23:135–140
  • Vanderauwera S, Zimmermann P, Rombauts S, Vandenabeele S, Langebartels C, Gruissem W, Inzè D, Van Breusegem F (2005) Genome-wide analysis of hydrogen peroxide-regulated gene expression in Arabidopsis reveals a high light-induced transcriptional cluster involved in anthocyanin biosynthesis. Plant Physiol 139:806–821
  • Vranova E, Atichartpongkul S, Villarroel R, Van Montagu M, Inzè D, Van Camp W (2002) Comprehensive analysis of gene expression in Nicotiana tabacum leaves acclimated to oxidative stress. Proc Natl Acad Sci USA 99:10870–10875
  • Wang Y, Ries A, Wu K, Yang A, Crawford NM (2010) The Arabidopsis prohibitin gene PHB3 functions in nitric oxidemediated responses and in hydrogen peroxide-induced nitric oxide accumulation. Plant Cell 22:249–259
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Bibliografia

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