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2012 | 34 | 6 |

Tytuł artykułu

Differential regulation of barley (Hordeum distichon) HVA1 and SRG6 transcript accumulation during the induction of soil and leaf water deficit

Warianty tytułu

Języki publikacji

EN

Abstrakty

EN
Drought tolerance in barley is highly correlated with the expression of two genes: Hordeum vulgare aleurone 1 (HVA1) and stress-responsive gene 6 (SRG6). Though their role in the mechanism of drought response in barley has been confirmed in transgenic plants, the regulation pathways of these genes’ expression have not been sufficiently studied, especially on the level of whole plants. We used four barley genotypes of different drought tolerance to establish and compare the expression profiles of SRG6 and HVA1 and to associate them with the possible physiological and biochemical signals of water deficit. Both genes studied were expressed to a greater extent in drought tolerant genotypes. The highest level of HVA1 transcript accumulation was observed under conditions where the leaf water potential decreased significantly. In tolerant genotype this signal was partially replaced with abscisic acid (ABA) signal of soil water deficit and the final transcript accumulation was about 14 times lower than in the case of leaf water deficit. In the case of SRG6 the main signal which can triggered the transcript accumulation was ABA but in the case of tolerant genotype the direct effect of leaf water deficit was also observed. Thus, it seems to be possible that in drought tolerant barley genotypes, HVA1 and SRG6, are not only more expressed during drought, but tolerant genotypes may be also more sensitive to various internal signals confirming environmental water deficit. The putative role of hydrogen peroxide as a signal of water deficit in the regulation of both genes expression was not confirmed. The drought-induced expression of both HVA1 and SRG6 was additionally reduced in the light. Because of this powerful complexity, a true understanding of plant response to drought requires further studies integrating gene expression and cell signaling analysis in single organs or tissues with whole plant physiology and long distance signaling.

Słowa kluczowe

Wydawca

-

Rocznik

Tom

34

Numer

6

Opis fizyczny

p.2069-2078,fig.,ref.

Twórcy

  • Department of Plant Physiology, University of Agriculture in Krakow, Podluzna 3, 30-239 Krakow, Poland
autor
  • Department of Plant Physiology, University of Agriculture in Krakow, Podluzna 3, 30-239 Krakow, Poland
autor
  • Department of Plant Physiology, University of Agriculture in Krakow, Podluzna 3, 30-239 Krakow, Poland
autor
  • Franciszek Gorski Institute of Plant Physiology, Polish Academy of Sciences, Niezapominajek 21, 30-239 Krakow, Poland

Bibliografia

  • Battaglia M, Olvera-Carrillo Y, Garciarrubio A, Campos F, Covarrubias AA (2008) The enigmatic LEA proteins and other hydrophilins. Plant Physiol 148:6–24
  • Bian S, Jiang Y (2009) Reactive oxygen species, antioxidant enzyme activities and gene expression patterns and recovery. Scientia Horticulare 120:264–270
  • Boudsocq M, Laurière C (2005) Osmotic signaling in plants. Multiple pathways mediated by emerging kinase families. Plant Physiol 138:1185–1194
  • Casaretto J, Ho T-HD (2003) The transcription factors HvABI5 and HvVP1 are required for the abscisic acid induction of gene expression in barley aleurone cells. Plant Cell 15:271–284
  • Cattivelli L, Rizza F, Badeck FW, Mazzucotelli E, Mastrangelo AM, Francia E, Marè C, Tondelli A, Stanca AM (2008) Drought tolerance improvement in crop plants: an integrated view from breeding to genomics. Field Crop Res 105:1–14
  • Foyer CH, Noctor G (2005) Oxidant and antioxidant signaling in plants: a revaluation the concept of oxidative stress in a physiological context. Plant Cell Environ 28:1056–1071
  • Genty B, Briantais J-M, Baker NR (1989) The relationship between the quantum yield of photosynthetic electron transport and quenching of chlorophyll fluorescence. Biochim Biophys Acta 990:87–92
  • Hong B, Uknes JS, Ho T-HD (1988) Cloning and characterization of a cDNA encoding a mRNA rapidly-induced by ABA in barley aleurone layers. Plant Mol Biol 11:495–506
  • Hong B, Barg R, Ho T-HD (1992) Developmental and organ-specific expression of an ABA- and stress-induced protein in barley. Plant Mol Biol 18:663–674
  • Jana S, Wilen RW (2005) Breeding for abiotic stress tolerance in barley. In: Ashraf M, Harris PJC (eds) Abiotic stresses. Plant resistance through breeding and molecular approaches. Haworth Press, New York, pp 491–511
  • Malatrasi M, Close TJ, Marmirolli N (2002) Identification and mapping of putative stress response regulator gene in barley. Plant Mol Biol 50:143–152
  • Maqbool SB, Zhong H, El-Maghraby Y, Ahmad A, Chai B, Wang W, Sabzikar R, Sticklen M (2002) Competence of oat (Avena sativa L.) shoot apical meristems for integrative transformation, inherited expression, and osmotic tolerance of transgenic lines containing hva1. Theor Appl Genet 105:201–208
  • Pfaffl MW (2001) A new mathematical model for relative quantification in real-time RT-PCR. Nucleic Acids Res 29:2002–2007
  • Pfannschmidt T, Bräutigam K, Wagner R, Dietzel L, Schröter Y, Steiner S, Nykytenko A (2009) Potential regulation of gene expression in photosynthetic cells by redox and energy state: approaches towards better understanding. Ann Bot 103:599–607
  • Rapacz M, Kościelniak J, Jurczyk B, Adamska A, Wójcik M (2010) Different patterns of physiological and molecular response to drought in seedlings of malt- and feedtype barleys (Hordeum vulgare). J Agron Crop Sci 196:9–19
  • Rock CD (2000) Pathways to abscisic acid-regulated gene expression. New Phytol 148:357–396
  • Schachtman DP, Goodger JQD (2008) Chemical root to shoot signaling under drought. Trends Plant Sci 13:281–287
  • Shen Q, Zhang P, Ho T-HD (1996) Modular nature of abscisic acid (ABA) response complexes: composite promoter units that are necessary and sufficient for ABA induction of gene expression in barley. Plant Cell 8:1107–1119
  • Sivamani E, Bahieldin A, Wraith JM et al (2000) Improved biomass productivity and water use efficiency under water deficit conditions in transgenic wheat constitutively expressing the barley HVA1 gene. Plant Sci 155:1–9
  • Tong S, Ni Z, Peng H, Dong G, Sun Q (2007) Ectopic overexpression of wheat TaSRG6 gene confers water stress tolerance in Arabidopsis. Plant Sci 172:1079–1086
  • Tuberosa R, Salvi S (2006) Genomics-based approaches to improve drought tolerance of crops. Trends Plant Sci 11:405–412
  • Vandenbroucke K, Robbens K, Vandepoele K, Inzé D, Van de Peer Y, Van Breusegem F (2008) Hydrogen peroxide–induced gene expression across kingdoms: A comparative analysis. Mol Biol Evol 25:507–516
  • Walker-Simmons MK, Abrams SR (1991) Use of ABA immunoassays. In: Davies WJ, Jones HG (eds) Abscisic acid, physiology and biochemistry. Bios Scientific Publishers, Oxford, pp 53–63
  • Xiao B, Huang Y, Tang N, Xiong L (2007) Over-expression of a LEA gene in rice improves drought resistance under the field conditions. Theor Appl Genet 115:3546
  • Xu Z, Zhou G, Shimizu H (2010) Plant responses to drought and rewatering. Plant Signal Behav 5:649–654
  • Yang S, Huang C, Wu Z (2006) Stomatal movement in response to long distance-communicated signals initiated by heat shock in partial roots of Commelina communis L. Sci China Ser C Life Sci 49:18–25

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