Isolation of ascorbate peroxidase (APX) gene in lentil (Lens culinaris Medik.) and expression analysis under drought stress conditions
Yıl 2022,
, 439 - 447, 30.09.2022
Melike Bakır
,
Cebrail Yıldırım
Öz
Objective: The objective of this study was to isolate partial cDNA that belongs to the ascorbate peroxidase (APX) gene of lentil (Lens culinaris Medik.) and to express LcAPX gene in lentil seedlings under drought stress conditions.
Material and Methods: To identify the relationships between drought stress and LcAPX gene expression, lentil seedlings grown for 2 weeks were subjected to drought stress through not irrigating for 6, 13, and 20 days. Effects of drought stress were determined by measuring the stem relative water content (RWC). Gene expression changes in lentil seedlings were determined with real-time RT-qPCR.
Results: The LcAPX gene expression levels of both drought-tolerant Firat-87 and drought-sensitive Ozbek cultivars varied with the severity of drought stress. The gene expression of LcAPX reached the highest level in Firat-87 cultivar on the 6th day, whereas a significant increase was observed only on the 20th day of the Ozbek cultivar, and this increase was relatively low as compared to the Fırat-87 cultivar.
Conclusion: From the study conducted, it was concluded that time-dependent changes of the expression of LcAPX gene indicates that LcAPX gene had a highly specific gene expression profile and complex regulation in lentil drought response.
Destekleyen Kurum
Erciyes Üniversitesi
Teşekkür
This study was supported by Erciyes University, Scientific Research Projects Unit (Project no: 6684). Thanks are extended to Betül-Ziya Eren Genome and Stem Cell Center of Erciyes University for their supports provided throughout the experiments.
Kaynakça
- Akbudak, M.A., E. Filiz, R. Vatansever & K. Kontbay, 2018. Genome-wide identification and expression profiling of ascorbate peroxidase (APX) and glutathione peroxidase (GPX) genes under drought stress in sorghum (Sorghum bicolor L.). Journal of Plant Growth Regulation, 37 (3): 925-936.
- Aksoy, E., 2008. Effect of Drought and Salt Stresses on The Gene Expression Levels of Antioxidant Enzymes in Lentil (Lens culinaris M.) Seedlings. University of Middle East Technical, (Unpublished) Master Thesis, Ankara, 207 pp.
- Arumuganathan, K. & E.D. Earle, 1991. Nuclear DNA content of some important plant species. Plant Molecular Biology Reporter, 9 (3): 208-218.
- Aslan, H., 2014. Effect of Chemical Foliar Application to Reduce Harvest Losses due to Pod Drop and Shatter in Red Lentil. Harran University, (Unpublished) Master Thesis, Şanlıurfa, 41 pp.
- Bahl, P.N., S. Lal & B.M. Sharma, 1993. “An overview of the production and problems in southeast Asia”. In: Proceedings of the seminar on lentils in South Asia. (Eds. W. Erskine & M.C. Saxena). ICARDA. Aleppo, Syria 236 pp.
- Bakır, M., 2019. Determination of Lentil (Lens culinaris M.) DEHYDRATION RESPONSIVE ELEMENT-BINDING2A (DREB2A) Gene Expression under Drought Stress Conditions. Journal of Agriculture Faculty of Ege University, 56 (2): 181-185.
- Barnabás, B., K. Jäger, & A. Fehér, 2008. The effect of drought and heat stress on reproductive processes in cereals. Plant, Cell & Environment, 31 (1): 11-38.
- Bartwal, A. & S. Arora, 2017. Drought stress-induced enzyme activity and mdar and apx gene expression in tolerant and susceptible genotypes of Eleusine coracana (L.). In Vitro Cellular & Developmental Biology-Plant, 53 (1): 41-49.
- Cao, S., X.H. Du, L.H. Li, Y.D. Liu, L. Zhang, X. Pan, Y. Li, H. Li & H. Lu, 2017. Overexpression of Populus tomentosa cytosolic ascorbate peroxidase enhances abiotic stress tolerance in tobacco plants. Russian Journal of Plant Physiology, 64 (2): 224-234.
- Ceritoğlu, M., 2019. The Effect of Vermicompost Applied at Different Sowing Dates on Yield and Yield Components in Lentil (Lens Culinaris Medik.). Siirt University, (Unpublished) Master Thesis, Siirt,102 pp.
- Çevik, S. & S. Ünyayar, 2015. The effects of exogenous application of ascorbate and glutathione on antioxidant system in cultivated Cicer arietinum and wild type C. reticulatum under drought stress. Journal of Natural & Applied Sciences, 19 (1): 91-97.
- Chen, G.X. & K., Asada, 1989. Ascorbate peroxidase in tea leaves: occurrence of two isozymes and the differences in their enzymatic and molecular properties. Plant and Cell Physiology, 30 (7): 987-998.
- Chugh, V., N. Kaur, M.S. Grewal & A.K. Gupta, 2013. Differential antioxidative response of tolerant and sensitive maize (Zea mays L.) genotypes to drought stress at reproductive stage. Indian Journal of Biochemistry & Biophysics, 50: 150.
- D'Arcy-Lameta, A., R. Ferrari-Iliou, D. Contour-Ansel, A.T. Pham-Thi & Y. Zuily-Fodil, 2006. Isolation and characterization of four ascorbate peroxidase cDNAs responsive to water deficit in cowpea leaves. Annals of Botany, 97 (1): 133-140.
- Dąbrowska, G., A. Kata, A. Goc, M. Szechyńska-Hebda & E. Skrzypek, 2007. Characteristics of the plant ascorbate peroxidase family. Acta Biologica Cracoviensia Series Botanica, 49 (1): 7-17.
- Elkoyunu, R., 2013. Effects of Different Chlorine Salts on Germination and Seedling Growth in Lentil (Lens esculanta Moench). Süleyman Demirel University, (Unpublished) Master Thesis, Isparta, 112 pp.
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- Güneş, A., S. Adak, A. İnal, M. Alpaslan, F. Eraslan, N. Çiçek & B. Soylu, 2006. Oxidatie Stress Depending on Drought and Determination Physiological Tolerance Mechanism in Chickpea and Lentil Cultivars. Scientific Research Project Final Report, 135 pp
- Harb, A., D. Awad & N. Samarah, 2015. Gene expression and activity of antioxidant enzymes in barley (Hordeum vulgare L.) under controlled severe drought. Journal of Plant Interactions, 10 (1): 109-116.
- Jaleel, C.A., P. Manivannan, A. Wahid, M. Farooq, H.J. Al-Juburi, R. Somasundaram & R. Panneerselvam, 2009. Drought stress in plants: a review on morphological characteristics and pigments composition. International Journal of Agriculture & Biology, 11 (1): 100-105.
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- Kausar, R., Z. Hossain, T. Makino & S. Komatsu, 2012. Characterization of ascorbate peroxidase in soybean under flooding and drought stresses. Molecular Biology Reports, 39 (12): 10573-10579.
- Köse, Ö.D.E., Y.M. Kardeş, M. Karaer & Z. Mut, 2019. Effects of Different Priming Techniques on Germination and Seedling Growth of Green Lentil (Lens culinaris Medik.) Cultivars. Bilecik Seyh Edebali University Journal of Science, 6: 247-255.
- Laxa, M., M. Liebthal, W. Telman, K. Chibani & K.J. Dietz, 2019. The role of the plant antioxidant system in drought tolerance. Antioxidants, 8 (4): 94.
- Li, Y.J., R.L. Hai, X.H. Du, X.N. Jiang & H. Lu, 2009. Over‐expression of a Populus peroxisomal ascorbate peroxidase (PpAPX) gene in tobacco plants enhances stress tolerance. Plant Breeding, 128 (4): 404-410.
- Livak, K.J. & T.D. Schmittgen, 2001. Analysis of relative gene expression data using real-time quantitative PCR and the 2− ΔΔCT method. Methods, 25 (4): 402-408.
- Marchin, R.M., A. Ossola, M.R. Leishman & D.S. Ellsworth, 2020. A simple method for simulating drought effects on plants. Frontiers in Plant Science, 10: 1715.
- Mittler, R. & B.A. Zilinskas, 1992. Molecular cloning and characterization of a gene encoding pea cytosolic ascorbate peroxidase. Journal of Biological Chemistry, 267 (30): 21802-21807.
- Mittler, R. & B.A. Zilinskas, 1994. Regulation of pea cytosolic ascorbate peroxidase and other antioxidant enzymes during the progression of drought stress and following recovery from drought. The Plant Journal, 5 (3): 397-405.
- Mittler, R., 2002. Oxidative stress, antioxidants and stress tolerance. Trends in Plant Science, 7 (9): 405-410.
- Miyake, C. & K. Asada, 1992. Thylakoid-bound ascorbate peroxidase in spinach chloroplasts and photoreduction of its primary oxidation product monodehydroascorbate radicals in thylakoids. Plant and Cell Physiology, 33 (5): 541-553.
- Morgil, H., M. Tardu, G. Cevahir & I.H. Kavakli, 2019. Comparative RNA-seq analysis of the drought-sensitive lentil (Lens culinaris) root and leaf under short-and long-term water deficits. Functional & Integrative Genomics, 19 (5): 715-727.
- Morita, S., H. Kaminaka, T. Masumura & K. Tanaka, 1999. Induction of rice cytosolic ascorbate peroxidase mRNA by oxidative stress; the involvement of hydrogen peroxide in oxidative stress signalling. Plant and Cell Physiology, 40 (4): 417-422.
- Muehlbauer, F.J., 1992. Use of introduced germplasm in cool‐season food legume cultivar development. Use of Plant Introductions in Cultivar Development, Part 2, 20: 49-73.
- Öktem, H.A., F. Eyidoðan, D. Demirba, A.T. Bayraç, M.T. Öz, E. Özgür, F. Selçuk & M. Yücel, 2008. Antioxidant responses of lentil to cold and drought stress. Journal of Plant Biochemistry and Biotechnology, 17 (1): 15-21.
- Örs, S. & M. Ekinci, 2015. Drought stress and plant physiology. Derim, 32 (2): 237-250.
- Oweis, T., A. Hachum & M. Pala, 2004. Lentil production under supplemental irrigation in a Mediterranean environment. Agricultural Water Management, 68 (3): 251-265.
- Pala, F., H. Mennan & A. Demir, 2018. Determination of the Weed Species, Frequency and Density in Lentil Fields in Diyarbakır Province. Turkish Journal of Weed Science, 21 (1): 33-42.
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Isolation of ascorbate peroxidase (APX) gene in lentil (Lens culinaris Medik.) and expression analysis under drought stress conditions
Yıl 2022,
, 439 - 447, 30.09.2022
Melike Bakır
,
Cebrail Yıldırım
Öz
Amaç: Bu çalışmada, mercimekte (Lens culinaris Medik.) askorbat peroksidaz (APX) geninin partial cDNA klonu izole edilmiş ve LcAPX geninin kuraklık stresi koşullarında mercimek fidelerinde değişen gen ifadesi seviyesi belirlenmiştir.
Materyal ve Yöntem: Kuraklık stresi ve LcAPX gen ifadesi arasındaki ilişkiyi anlamak için, 2 hafta süre ile yetiştirilen mercimek fidelerine 6, 13 ve 20 gün süre ile sulamama şeklinde kuraklık stresi uygulanmıştır. Kuraklık stresinin etkileri, sap nispi nem içeriği (RWC) ölçülerek belirlenmiştir. Mercimek fidelerinde meydana gelen gen ifadesi değişimleri eş zamanlı kantitatif PCR (Real-time qPCR) ile belirlenmiştir.
Araştırma Bulguları: Hem kuraklığa dayanıklı Fırat-87 hem de kuraklığa duyarlı Özbek çeşitlerinin LcAPX gen ekspresyon seviyeleri, kuraklık stresinin şiddetine göre değişiklik göstermiştir. LcAPX gen ekspresyonu Fırat-87 çeşidinde 6. günde en yüksek seviyeye ulaşırken, Özbek çeşidinin sadece 20. gününde önemli bir artış gözlenmiş ve bu artış Fırat-87 çeşidine göre nispeten düşük kalmıştır.
Sonuç: Sonuç olarak, LcAPX geninin ekspresyonunun gün bazında değişmesi, LcAPX geninin mercimeğin kuraklığa tepkisinde oldukça spesifik bir gen ekspresyon profiline ve karmaşık bir regülasyona sahip olduğunu göstermektedir.
Kaynakça
- Akbudak, M.A., E. Filiz, R. Vatansever & K. Kontbay, 2018. Genome-wide identification and expression profiling of ascorbate peroxidase (APX) and glutathione peroxidase (GPX) genes under drought stress in sorghum (Sorghum bicolor L.). Journal of Plant Growth Regulation, 37 (3): 925-936.
- Aksoy, E., 2008. Effect of Drought and Salt Stresses on The Gene Expression Levels of Antioxidant Enzymes in Lentil (Lens culinaris M.) Seedlings. University of Middle East Technical, (Unpublished) Master Thesis, Ankara, 207 pp.
- Arumuganathan, K. & E.D. Earle, 1991. Nuclear DNA content of some important plant species. Plant Molecular Biology Reporter, 9 (3): 208-218.
- Aslan, H., 2014. Effect of Chemical Foliar Application to Reduce Harvest Losses due to Pod Drop and Shatter in Red Lentil. Harran University, (Unpublished) Master Thesis, Şanlıurfa, 41 pp.
- Bahl, P.N., S. Lal & B.M. Sharma, 1993. “An overview of the production and problems in southeast Asia”. In: Proceedings of the seminar on lentils in South Asia. (Eds. W. Erskine & M.C. Saxena). ICARDA. Aleppo, Syria 236 pp.
- Bakır, M., 2019. Determination of Lentil (Lens culinaris M.) DEHYDRATION RESPONSIVE ELEMENT-BINDING2A (DREB2A) Gene Expression under Drought Stress Conditions. Journal of Agriculture Faculty of Ege University, 56 (2): 181-185.
- Barnabás, B., K. Jäger, & A. Fehér, 2008. The effect of drought and heat stress on reproductive processes in cereals. Plant, Cell & Environment, 31 (1): 11-38.
- Bartwal, A. & S. Arora, 2017. Drought stress-induced enzyme activity and mdar and apx gene expression in tolerant and susceptible genotypes of Eleusine coracana (L.). In Vitro Cellular & Developmental Biology-Plant, 53 (1): 41-49.
- Cao, S., X.H. Du, L.H. Li, Y.D. Liu, L. Zhang, X. Pan, Y. Li, H. Li & H. Lu, 2017. Overexpression of Populus tomentosa cytosolic ascorbate peroxidase enhances abiotic stress tolerance in tobacco plants. Russian Journal of Plant Physiology, 64 (2): 224-234.
- Ceritoğlu, M., 2019. The Effect of Vermicompost Applied at Different Sowing Dates on Yield and Yield Components in Lentil (Lens Culinaris Medik.). Siirt University, (Unpublished) Master Thesis, Siirt,102 pp.
- Çevik, S. & S. Ünyayar, 2015. The effects of exogenous application of ascorbate and glutathione on antioxidant system in cultivated Cicer arietinum and wild type C. reticulatum under drought stress. Journal of Natural & Applied Sciences, 19 (1): 91-97.
- Chen, G.X. & K., Asada, 1989. Ascorbate peroxidase in tea leaves: occurrence of two isozymes and the differences in their enzymatic and molecular properties. Plant and Cell Physiology, 30 (7): 987-998.
- Chugh, V., N. Kaur, M.S. Grewal & A.K. Gupta, 2013. Differential antioxidative response of tolerant and sensitive maize (Zea mays L.) genotypes to drought stress at reproductive stage. Indian Journal of Biochemistry & Biophysics, 50: 150.
- D'Arcy-Lameta, A., R. Ferrari-Iliou, D. Contour-Ansel, A.T. Pham-Thi & Y. Zuily-Fodil, 2006. Isolation and characterization of four ascorbate peroxidase cDNAs responsive to water deficit in cowpea leaves. Annals of Botany, 97 (1): 133-140.
- Dąbrowska, G., A. Kata, A. Goc, M. Szechyńska-Hebda & E. Skrzypek, 2007. Characteristics of the plant ascorbate peroxidase family. Acta Biologica Cracoviensia Series Botanica, 49 (1): 7-17.
- Elkoyunu, R., 2013. Effects of Different Chlorine Salts on Germination and Seedling Growth in Lentil (Lens esculanta Moench). Süleyman Demirel University, (Unpublished) Master Thesis, Isparta, 112 pp.
- FAOSTAT, 2018. Food and Agriculture Organization (FAO) Stats. (Web page: http: //www.fao.org/faostat/en/#data/QC/visualize) (Date accessed: 03 March 2020).
- Ghaderi, N., A.R. Talaie, A. Ebadi & H. Lessani, 2011. The physiological response of three Iranian grape cultivars to progressive drought stress. Journal of Agricultural and Technology, 13 (4): 601-610.
- Gökçay, D., 2012. Physiological and Biochemical Screeing of Different Turkish Lentil (Lens culinaris M.) Cultivars under Drought Stress Condition. Master Thesis, Middle East Tecnical University, (Unpublished) Master Thesis, Ankara, 80 pp.
- Güneş, A., S. Adak, A. İnal, M. Alpaslan, F. Eraslan, N. Çiçek & B. Soylu, 2006. Oxidatie Stress Depending on Drought and Determination Physiological Tolerance Mechanism in Chickpea and Lentil Cultivars. Scientific Research Project Final Report, 135 pp
- Harb, A., D. Awad & N. Samarah, 2015. Gene expression and activity of antioxidant enzymes in barley (Hordeum vulgare L.) under controlled severe drought. Journal of Plant Interactions, 10 (1): 109-116.
- Jaleel, C.A., P. Manivannan, A. Wahid, M. Farooq, H.J. Al-Juburi, R. Somasundaram & R. Panneerselvam, 2009. Drought stress in plants: a review on morphological characteristics and pigments composition. International Journal of Agriculture & Biology, 11 (1): 100-105.
- Jiang, Y., E. Watkins, S. Liu, X. Yu & N. Luo, 2010. Antioxidative responses and candidate gene expression in prairie junegrass under drought stress. Journal of the American Society for Horticultural Science, 135 (4): 303-309.
- Joshi, R. & R. Karan, 2013. “Physiological, Biochemical and Molecular Mechanisms of Drought Tolerance in Plants, 318-338”. In: Molecular Approaches in Plant Abiotic Stress, (Eds. R. K. Gaur & P. Sharma) Boca Raton, FL: CRC Press 430 pp.
- Kabay, T. & S. Şensoy, 2016. Enzyme, Chlorophyl and Ion Changes in Some Common Bean Genotypes by Drought Stress. Yuzuncu Yıl University Journal of Agricultural Sciences, 26 (3): 380-395.
- Kalefetoğlu, T. & Y. Ekmekci, 2005. The effects of drought on plants and tolerance mechanisms. Gazi University Journal of Science, 18 (4): 723-740.
- Kausar, R., Z. Hossain, T. Makino & S. Komatsu, 2012. Characterization of ascorbate peroxidase in soybean under flooding and drought stresses. Molecular Biology Reports, 39 (12): 10573-10579.
- Köse, Ö.D.E., Y.M. Kardeş, M. Karaer & Z. Mut, 2019. Effects of Different Priming Techniques on Germination and Seedling Growth of Green Lentil (Lens culinaris Medik.) Cultivars. Bilecik Seyh Edebali University Journal of Science, 6: 247-255.
- Laxa, M., M. Liebthal, W. Telman, K. Chibani & K.J. Dietz, 2019. The role of the plant antioxidant system in drought tolerance. Antioxidants, 8 (4): 94.
- Li, Y.J., R.L. Hai, X.H. Du, X.N. Jiang & H. Lu, 2009. Over‐expression of a Populus peroxisomal ascorbate peroxidase (PpAPX) gene in tobacco plants enhances stress tolerance. Plant Breeding, 128 (4): 404-410.
- Livak, K.J. & T.D. Schmittgen, 2001. Analysis of relative gene expression data using real-time quantitative PCR and the 2− ΔΔCT method. Methods, 25 (4): 402-408.
- Marchin, R.M., A. Ossola, M.R. Leishman & D.S. Ellsworth, 2020. A simple method for simulating drought effects on plants. Frontiers in Plant Science, 10: 1715.
- Mittler, R. & B.A. Zilinskas, 1992. Molecular cloning and characterization of a gene encoding pea cytosolic ascorbate peroxidase. Journal of Biological Chemistry, 267 (30): 21802-21807.
- Mittler, R. & B.A. Zilinskas, 1994. Regulation of pea cytosolic ascorbate peroxidase and other antioxidant enzymes during the progression of drought stress and following recovery from drought. The Plant Journal, 5 (3): 397-405.
- Mittler, R., 2002. Oxidative stress, antioxidants and stress tolerance. Trends in Plant Science, 7 (9): 405-410.
- Miyake, C. & K. Asada, 1992. Thylakoid-bound ascorbate peroxidase in spinach chloroplasts and photoreduction of its primary oxidation product monodehydroascorbate radicals in thylakoids. Plant and Cell Physiology, 33 (5): 541-553.
- Morgil, H., M. Tardu, G. Cevahir & I.H. Kavakli, 2019. Comparative RNA-seq analysis of the drought-sensitive lentil (Lens culinaris) root and leaf under short-and long-term water deficits. Functional & Integrative Genomics, 19 (5): 715-727.
- Morita, S., H. Kaminaka, T. Masumura & K. Tanaka, 1999. Induction of rice cytosolic ascorbate peroxidase mRNA by oxidative stress; the involvement of hydrogen peroxide in oxidative stress signalling. Plant and Cell Physiology, 40 (4): 417-422.
- Muehlbauer, F.J., 1992. Use of introduced germplasm in cool‐season food legume cultivar development. Use of Plant Introductions in Cultivar Development, Part 2, 20: 49-73.
- Öktem, H.A., F. Eyidoðan, D. Demirba, A.T. Bayraç, M.T. Öz, E. Özgür, F. Selçuk & M. Yücel, 2008. Antioxidant responses of lentil to cold and drought stress. Journal of Plant Biochemistry and Biotechnology, 17 (1): 15-21.
- Örs, S. & M. Ekinci, 2015. Drought stress and plant physiology. Derim, 32 (2): 237-250.
- Oweis, T., A. Hachum & M. Pala, 2004. Lentil production under supplemental irrigation in a Mediterranean environment. Agricultural Water Management, 68 (3): 251-265.
- Pala, F., H. Mennan & A. Demir, 2018. Determination of the Weed Species, Frequency and Density in Lentil Fields in Diyarbakır Province. Turkish Journal of Weed Science, 21 (1): 33-42.
- Panchuk, I.I., R.A. Volkov & F. Schöffl, 2002. Heat stress-and heat shock transcription factor-dependent expression and activity of ascorbate peroxidase in Arabidopsis. Plant Physiology, 129 (2): 838-853.
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