Journals / Tarla Bitkileri Merkez Araştırma Enstitüsü Dergisi / 2016 / Cilt: 25 - Sayı: 1

The Role of the Relationship between Hydrogen Peroxide and Nitric Oxide in Plant Tolerance to Abiotic Stresses

Hidrojen Peroksit ve Nitrik Oksit İlişkisinin Bitkilerde Abiyotik Stres Toleransındaki Rolü

Pages
117–131
DOI
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

In addition, the cross-talk between H2O2and NO with other signalling pathways in the regulationof abiotic stress responses in plants is also discussed

📌 3 Key Takeaways

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Objective & Hypothesis:Hydrogen peroxide (H) and Nitric oxide (NO) are signalling molecules that play an important role indifferent organisms.
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Key Findings & Data:In this paper, HO2and NO cross-talk and possible role in plantresponses to abiotic stresses such as drought, salinity, extreme temperatures, UV irradiation and heavymetals at the level of biosynthesis and gene expression and protein activities are investigated in light of recentliterature.
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Conclusion & Impact:In addition, the cross-talk between H2O2and NO with other signalling pathways in the regulationof abiotic stress responses in plants is also discussed
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Hydrogen peroxide (H) and Nitric oxide (NO) are signalling molecules that play an important role indifferent organisms. Even though intensive research in the past two decades, knowledge about the role ofthese two molecules interact with each other in abiotic stress tolerance and the relationship with biologicalprocesses aren’t completely elucidated yet. In this paper, HO2and NO cross-talk and possible role in plantresponses to abiotic stresses such as drought, salinity, extreme temperatures, UV irradiation and heavymetals at the level of biosynthesis and gene expression and protein activities are investigated in light of recentliterature. In addition, the cross-talk between H2O2and NO with other signalling pathways in the regulationof abiotic stress responses in plants is also discussed

Özet

Hidrojen peroksit (H2O2) ve Nitrik oksit (NO), çeşitli organizmalarda önemli etkileri bulunan sinyal iletimmolekülleridir. Son 20 yıldır yapılan yoğun çalışmalara rağmen, abiyotik stres toleransında bu iki molekülünbirbirleriyle olan etkileşimlerinin rolü ve oluşturdukları sinyallerin biyolojik süreçlerle ilişkileri konusundaki bilgilergünümüzde de sınırlı düzeydedir. Bu makalede bitkilerin kuraklık, tuzluluk, aşırı sıcaklık, UV ışığı ve ağır metallergibi abiyotik strese tepkide H2O2ve NO etkileşiminin muhtemel rolleri biyosentez, gen ifadesi ve proteinaktiviteleri düzeyinde son literatür verileri ışığında araştırılmıştır. Ayrıca bitkilerde abiyotik stres yanıtlarında yeralan diğer sinyal iletim yolakları ile H2Ove NO'nun arasındaki etkileşimler tartışılmıştır

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Cite This Article

ÖZDAMAR, F. Ö., FURTANA, G. B., ELLİALTIOĞLU, Ş. Ş., TIPIRDAMAZ, R. (2016). The Role of the Relationship between Hydrogen Peroxide and Nitric Oxide in Plant Tolerance to Abiotic Stresses. Tarla Bitkileri Merkez Araştırma Enstitüsü Dergisi, Cilt: 25 - Sayı: 1, 117–131. https://ajindex.com/articles/360603

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References (9)

  1. Abogadallah G.M., 2010.Antioxidative defense under salt stress. Plant Signalling Behaviour, 5: 369– 374 Avsian-Kretchmer O., Gueta-Dahan Y., Lev-Yadun S., Gollop R. and Ben-Hayyim G., 2004. The saltstress signal transduction pathway that activates the gpx1 pro-moter is mediated by intracellular H2O2,different from the pathway induced byextracellular H2O2 Plant Physiology, 135: 1685–1696 Bajguz A. and Hayat S., 2009. Effects of brassinosteroids on the plant responses to environmental stresses. Plant Physiology and Biochemistry, 47: 1–8
  2. Banti V., Mafessoni, F., Loreti E.,AlpiA. and Perata P., 2010. The heat-inducible transcription factor HsfA2 enhances anoxia tolerance in Arabidopsis. Plant Physiology, 152: 1471– 1483 Beligni M. V. and Lamattina L. 1999. Is nitric oxide toxic or protective? Trends in Plant Science, 4: 299–300
  3. Besson-Bard A., Courtois C. and Gauthier A., 2008. Nitric Oxide in Plants: Production and crosstalk with Ca2+ signalling, Plant Molecular Biology, 1: 218-228
  4. Bethke P. C., Badger M.R. and Jones R. L. 2004. Apoplastic synthesis of nitric oxide by plant tissues. Plant Cell, 16: 332–341 Blokhina O. and Fagerstedt KV., 2010. Reactive oxygen species and nitric oxide in plant mitochondria: origin and redundant regulatory systems. Physiologia Plantarum, 138:447–462 Bouchard J.N. and Yamasaki H., 2009. Implication of nitric oxide in the heat-stress-induced cell death of the symbiotic alga Symbiodinium microadriaticum Marine Biology 156: 2209– 2220 Bright J., Desikan R., Hancock J.T., Weir I.S., Neill, S.J., 2006. ABA-induced NO generation and stomatal closure in Arabidopsis are dependent on H2O2 synthesis. The Plant Journal. 4: 113–122
  5. Broniowska K. A., Diers A.R. and Hogg N., 2013. S - Nitrosoglutathione. Biochimica et Biophysica Acta, 1830: 3173–3181
  6. Büyük I., Soydam-Aydın S. ve Aras S., 2012. Bitkilerin Tuz Stresine Verdiği Moleküler Cevaplar, Türk Hijyen ve Deneysel Biyoloji Dergisi, 69 (2): 97-110
  7. Clarke A., Desikan R., Hurst R.D., Hancock, J.T. and Neill, S.J., 2000. NO way back: nitric oxide and programmed cell death in Arabidopsis thaliana suspension cultures. The Plant Journal, 24: 667–677
  8. Cooney R.V., Harwood P.J., Custer L.J. and Franke A.A. 1994. Light mediated conversion of nitrogen dioxide to nitric oxide by carotenoids. Environ Health Perspectives, 102:460–462
  9. Corpas F.J., Barroso J.B. and Carreras A., 2004. Cellular and subcellular localization of endogenous nitric oxide in young and senescent pea plants. Plant Physiology, 136:2