The effect of abscisic acid on cold tolerance and chloroplasts ultrastructure in wheat under optimal and cold stress conditions

详细信息    查看全文

• 作者：Yuliya Venzhik ; Vera Talanova ; Alexandr Titov
• 关键词：Triticum aestivum ; Abscisic acid ; Cold tolerance ; Ultrastructure of chloroplast
• 刊名：Acta Physiologiae Plantarum
• 出版年：2016
• 出版时间：March 2016
• 年：2016
• 卷：38
• 期：3
• 全文大小：1,585 KB
• 参考文献：Akter K, Kato M, Sato Y, Kaneco Y, Takezawa D (2014) Abscisic acid-induced rearrangement of intracellular structures associated with freezing and desiccation tress tolerance in the liverwort Marchantia polymorpha. J Plant Physiol 171:1334–1343CrossRef PubMed
  Aroca R, Vernieri P, Irigoyen JJ, Sánchez-Diaz M, Tognoni F, Pardossi A (2003) Involvement of abscisic acid in leaf and root of maize (Zea mays L.) in avoiding chilling-induced water stress. Plant Sci 165:671–679CrossRef
  Asthir B, Kaur S, Mann SK (2009) Effect of salicylic and abscisic acid administered through detached tiller on antioxidand system in developing wheat grains under heat stress. Acta Physiol Plant 31:1091–1109CrossRef
  Badowiek A, Świgonska S, Szypulka E, Weidner S (2012) Influence of exogenous abscisic acid on alterations in protein expression in the proteome of Triticosecale seedlings. Acta Physiol Plant 6(34):2359–2368CrossRef
  Bakht J, Bano A, Dominy P (2006) The role of abscisic acid and low temperature in in chickpea (Cicer arientum) cold tolerance. II. Effect on plasma membrane structure and function. J Exp Bot 57:3707–3715CrossRef PubMed
  Bohn M, Lüthje S, Sperling P, Heinz E, Dörffling K (2007) Plasma membrane lipid alterations induced by cold acclimation and abscisic acid treatment of winter wheat seedlings differing in frost resistance. J Plant Physiol 164:146–156CrossRef PubMed
  Catalá R, Salinas J (2010) Temperature-perception, molecules and mechanisms. J Appl Biomed 8:189–198CrossRef
  Chen WP, Li PH (2002) Membrane stabilization by abcsicic acid under cold aids proline in alleviating chilling injury in maize (Zea mays L.). Plant Cell Environ 25:955–962CrossRef
  Chono M, Matsunaka H, Seki M, Fujita M, Kiribuchi-Otobe C, Oda S, Kojima H, Kobayashi D, Kawakami N (2013) Isolation of a wheat (Triticum aestivum L.) mutant in ABA 8′-hydroxylase gene: effect of reduced ABA catabolism on germination inhibition under field condition. Breed Sci 63:104–115PubMedCentral CrossRef PubMed
  Corrêa de Souza T, Magalhães PC, Mauro de Castro E, Pereira de Albuquerque PE, Marabesi MA (2013) The influence of ABA on water relation, photosynthesis parameters, and chlorophyll fluorescence under drought conditions in two maize hybrids with contrasting drought resistance. Acta Physiol Plant 35:515–527CrossRef
  Crosatti C, Rizza F, Badeck FW, Mazzucotelli E, Cattivelli L (2013) Harden the chloroplast to protect the plant. Physiol Plant 147:55–63CrossRef PubMed
  Dallaire S, Houde M, Gagné Y, Saini HS, Boileau S, Chevrier N, Sarhan F (1994) ABA and low temperature induce freezing tolerance via distinct regulatory pathways in wheat. Plant Cell Physiol 35:1–9
  Ensminger I, Busch F, Huner N (2006) Photostasis and cold acclimation: sensing low temperature through photosynthesis. Physiol Plant 126:28–44CrossRef
  Flores-Nimedes AA, Dörffling K, Vergara BS (1993) Improvement of chilling resistance in rice by application of an abscisic acid analog in combination with the growth retardant tetcyclacis. J Plant Growth Regul 12:27–34CrossRef
  Garbero M, Pedranzani H, Zirulnik F, Molina A, Péres-Chaca MV, Vigliocco A, Abdala G (2011) Short-term cold stress in two cultivars of Digitaria eriantha: effects on stress-related hormones and antioxidant defense system. Acta Physiol Plant 33:497–507CrossRef
  Garbero M, Andrade A, Reinoso H, Fernández B, Cuesta C, Granda V, Escudero C, Abdala G, Pedranzani H (2012) Differential effect of short-term cold stress on growth, anatomy, and hormone levels in cold-sensitive versus resistance cultivars of Digiteria eriantha. Acta Physiol Plant 34:2079–2091CrossRef
  Goral TK, Johnson MP, Duffy CD, Brain PR, Ruban AV (2012) Light-harvesting antenna composition controls the macrostructure and dynamics of thylakoid membrane in Arabidopsis. Plant J 69:289–301CrossRef PubMed
  Gray CG, Hansen MR, Shau DJ, Graham K, Dale R, Natesan SKA, Newell CA (2012) Plastid stromules are induced by stress treatments acting through abscisic acid. Plant J 69:387–398CrossRef PubMed
  Guo WL, Chen RG, Gong ZH, Yin YX, Ahmed SS, He YM (2012) Exogenous abscisic acid increases antioxidant enzymes and related gene expression in pepper (Capsicum annuum) leaves subjected to chilling stress. Genet Mol Res 11:4063–4080CrossRef PubMed
  Guóth A, Benyó D, Csiszár J, Gallé Á, Horváth F, Cseur L, Erdey L, Tari I (2010) Relatioship between osmotic stress-induced abscisic acid accumulation, biomass production and plant growth in drought-tolerance and -sensitive wheat cultivars. Acta Physiol Plant 32:719–727CrossRef
  Gusta LV, Trischuk R, Weiser CJ (2005) Plant cold acclimation: the role of abscisic acid. J Plant Growth Regul 24:308–318CrossRef
  Heidarvand L, Amiri M (2010) What happens in plant molecules responses to cold stress. Acta Physiol Plant 32:419–431CrossRef
  Huner NPM, Öquist G, Sarhan F (1998) Energy balance and acclimation to light and cold. Trends Plant Sci 3:1360–1385CrossRef
  Janmohammadi M, Enayati V, Sabaghnia N (2012) Impact of cold acclimation, de-acclimation and re-acclimation on carbohydrate content and antioxidant enzyme activities in spring and winter wheat. Icel Agric Sci 25:3–11
  Khatoon M, Inagawa K, Pospisil P, Yamashita A, Yoshioka M, Lundin B, Horie J, Morita N, Yamamoto Y, Yamamoto Y (2009) Quality control of photosystem II thylakoid unstacking is necessary to avoid further damage to the D1 protein and to facilitate D1 degradation under light stress in spinach thylakoids. J Biol Chem 284:25343–25352PubMedCentral CrossRef PubMed
  Klíma M, Vítámvás P, Selenková S, Vyvadilová M, Prášil IT (2012) Dehydrin and proline content in Brassica napus and B. carinata under cold stress at two irradiances. Biol Plant 56:157–161CrossRef
  Kobayashi F, Takumi S, Nakamura C (2008) Increased freezing tolerance in an ABA-hypersensitive mutant of common wheat. J Plant Physiol 165:224–232CrossRef PubMed
  Koleva D, Ganeva Ts, Stefanova M (2013) Effect of ABA pretreatment on chloroplast structure in Hypericum rumeliacum Boiss. plants subjected to cryopreservation. Bulg J Agric Sci 19:18–21
  Kovács Z, Simon-Sarcadi L, Szűcz A, Kocsy G (2010) Differential effects of cold, osmotic stress and abscisic acid on polyamine accumulation in wheat. Amino Acids 38:623–631CrossRef PubMed
  Kratsch HA, Wise RR (2000) The ultrastructure of chilling stress. Plant Cell Environ 23:337–350CrossRef
  Kutik J, Hola D, Kocova M, Rothova O, Haise D, Wilhelmova N, Ticha I (2004) Ultrastructure and dimensions of chloroplasts in leaves of three maize (Zea mays L.) inbred lines and their F1 hybrids grown under moderate chilling stress. Photosynthetica 42:447–455CrossRef
  Liu F, Jensen CR, Andersen MN (2005) A review of drought adaptation in crop plants: changes in vegetative and reproductive physiology induced by ABA-dased chemical signals. Aust J Agric Res 56:1245–1252CrossRef
  Mäntylä E, Lång V, Palva ET (1995) Role of abscisic acid in drought-induced freezing tolerance, cold acclimation, and accumulation of LTI78 and RAB18 proteins in Arabidopsis thaliana. Plant Physiol 107:141–148PubMedCentral PubMed
  Morillon R, Chrispeels MJ (2001) The role of ABA and the transpiration stream in the regulation of the osmotic water permeability of leaf cells. Proc Natl Acad Sci USA 98:14138–14143PubMedCentral CrossRef PubMed
  Murata N, Takahashi S, Nishiyama Y, Allakhverdiev SI (2007) Photoinhibition of photosystem II under environmental stress. Biochim Biophys Acta 1767:414–421CrossRef PubMed
  Nayyar H, Walia DP (2003) Water stress induced proline accumulation in contrasting wheat genotypes as affected by calcium and abscisic acid. Biol Plant 46:275–279CrossRef
  Pastorczyk M, Gielwanowska I, Lahuta LB (2014) Changes in soluble carbohydrates in polar Caryophyllaceae and Poaceae plants in response to chilling. Acta Physiol Plant 36:1771–1780CrossRef
  Pribil M, Labs M, Leister D (2014) Structure and dynamics of thylakoids in land plants. J Exp Bot 65:1955–1972CrossRef PubMed
  Qin F, Shinozaki K, Yamaguchi- Shinozaki K (2011) Achievements and challenges in understanding plant abiotic stress responses and tolerance. Plant Cell Physiol 52:1569–1582CrossRef PubMed
  Rook F, Hadingham SA, Li Y, Bevan MW (2006) Sugar and ABA response pathways and the control of gene expression. Plant Cell Environ 29:426–434CrossRef PubMed
  Roychoundhury A, Paul S, Basu S (2013) Cross-talk between abscisic acid-dependent and abscisic acid-independent pathways during abiotic stress. Plant Cell Rep 32:985–1006CrossRef
  Ruelland E, Zachowsky A (2010) How plant sense temperature. Environ Exp Bot 69:225–232CrossRef
  Saibo NJ, Lourenço T, Oliveria MM (2009) Transcription factors and regulation of photosynthesis and related metabolism under environmental stresses. Ann Botany 103:609–623CrossRef
  Shakirova FM, Bezrukova MV, Shayakhmetov IF (1996) Effect of temperature shock on the dynamics of abscisic acid and wheat germ agglutinin accumulation in wheat cell culture. Plant Growth Regul 19:85–87CrossRef
  Talanova VV, Titov AF, Topchieva LV, Malysheva IE, Venzhik YuV, Frolova SA (2009) Expression of WRKY transcription factor and stress protein genes in wheat plants during cold hardening and ABA treatment. Russ J Plant Physiol 56:702–708CrossRef
  Teng K, Li J, Liu L, Han Y, Du Y, Zhang J, Sun H, Zhao Q (2014) Exogenous ABA induced drought tolerance in upland rice: the role of chloroplast and ABA biosynthesis-related gene expression on photosystem II during PEG stress. Acta Physiol Plant 36:2219–2227CrossRef
  Titov AF, Talanova VV, Akimova TV (2003) The effect of root treatment with various stress agents on plant cold- and heat tolerance. Russ J Plant Physiol 50:94–99CrossRef
  Travaglia C, Cohen AC, Reinoso H, Castillo C, Bottini R (2007) Exogenous abscisic acid increases carbohydrate accumulation and redistribution to the grains in wheat grown under field conditions os soil water restriction. J Plant Growth Regul 26:285–289CrossRef
  Tsuda K, Tsvetanov S, Takumi S, Mor N, Atanassov A, Nakamura C (2000) New members of a cold-responsive Group-3 Lea/Rab-related Cor gene family from common wheat (Triticum aestivum L.). Gen Genet Syst 75:179–188CrossRef
  Venzhik YV, Titov A, Talanova VV, Miroslavov EA, Koteeva NK (2013) Structural and functional reorganization of the photosynthetic apparatus in adaptation to cold of wheat plants. Cell Tissue Biol 7:168–176CrossRef
  Venzhik YV, Titov AF, Talanova VV, Miroslavov EA (2014) Ultrastructure and functional activity of chloroplasts in wheat leaves under root chilling. Acta Physiol Plant 36:323–330CrossRef
  Wang T, Zhang X, Li C (2007) Growth, abscisic acid content, and carbon isotope composition in wheat cultivars grown under different soil moisture. Biol Plant 51:181–184CrossRef
  Wang G-L, Miao W, Wang JY, Ma D-R, Li J-Q, Chen W-F (2013) Effect of exogenous abscisic acid on antioxidant system in weedy and cultivated rice with different chilling sensitivity under chilling stress. J Agron Crop Sci 199:200–208CrossRef
  Wilkinson S, Davies WJ (2002) ABA-based chemical signaling: the coordination of responses to stress in plants. Plant Cell Environ 25:195–210CrossRef PubMed
  Wu J, Lightner J, Warwick N, Browse J (1997) Low-temperature damage and subsequent recovery of fab1 mutant Arabidopsis exposed to 2 °C. Plant Physiol 113:347–356PubMedCentral CrossRef PubMed
  Yamamoto Y, Kai S, Ohnishi A, Tsumura N, Ishikawa T, Hori H, Morita N, Ishikawa Y (2014) Quality control of PSII in the highly crowded grana thylakoids under excessive light. Plant Cell Physiol 55:1206–1215PubMedCentral CrossRef PubMed
  Yamburenko MV, Zubo YO, Vanková R, Kusnetsov VV, Kulaeva ON, Börner T (2013) Abscisic acid represses the transcription of chloroplast genes. J Exp Bot 64:4491–4502PubMedCentral CrossRef PubMed
  Zhang J, Jia W, Yang J (2004) ABA in plant water stress signaling. Proc Indian Natl Sci Acad 70:367–377
  Zhou B, Guo Z, Lin L (2006) Effects of abscisic acid application on photosynthesis and photochemistry of Stylosanthes guianensis under chilling stress. Plant Growth Regul 48:195–199
  
• 作者单位：Yuliya Venzhik (1)
  Vera Talanova (1)
  Alexandr Titov (1)
  
  1. Institute of Biology, Karelian Research Centre, Russian Academy of Sciences, Petrozavodsk, Russian Federation
  
• 刊物主题：Plant Physiology; Plant Genetics & Genomics; Plant Biochemistry; Plant Pathology; Plant Anatomy/Development; Agriculture;
• 出版者：Springer Berlin Heidelberg
• ISSN：1861-1664

文摘

The effect of abscisic acid (0.1 mM) on cold tolerance of leaf cells and ultrastructure of chloroplasts in wheat (Triticum aestivum L.) under optimal (22 °C) and cold stress conditions (4 °C) was studied. Results indicated that exogenous abscisic acid induces a rise in the cold tolerance of wheat along with a number of significant ultrastructural changes in chloroplasts both at 22 and at 4 °C. Some of them (increase in density of chloroplasts stroma, formation of “distorted” and “dilated” thylakoids, appearance of invaginations, changes in the shape of chloroplasts and increase of their dimension owing to the stroma area) were common to the two types of treatments. At the same time, the character of changes in the membrane system of plastids was temperature specific, i.e. if at 22 °C the hormone caused a considerable increase in the length of photosynthetic membranes in chloroplast owing the length of both appressed and non-appressed membranes of thylakoids, then in cold stress conditions observed an increase in the number of grana and the length of appressed membranes of thylakoids. These results suggested that the rise in the cold tolerance of abscisic acid-treated plants is associated with the ultrastructural reorganization of chloroplasts aimed to defense plant cells against chilling injury and to maintain the activity of the photosynthetic system. Keywords Triticum aestivum Abscisic acid Cold tolerance Ultrastructure of chloroplast