Differential organ specific protein profiling in chickpea cultivars under water deficit stress

Authors

  • DAVINDER KAUR Punjab Agricultural University, Ludhiana-141004, India Author
  • SATVIR KAUR GREWAL Punjab Agricultural University, Ludhiana-141004, India Author
  • JAGMEET KAUR Punjab Agricultural University, Ludhiana-141004, India Author
  • SARVJEET SINGH Punjab Agricultural University, Ludhiana-141004, India Author

DOI:

https://doi.org/10.59797/journaloffoodlegumes.v31i1.443

Keywords:

Chickpea, Protein profile, Water deficit stress

Abstract

Chickpea is an important legume crop but its yield is highly affected by water deficit stress. It has been reported that many proteins related to stress/defence/detoxification, carbohydrate metabolism and photosynthesis are crucial for imparting water deficit stress tolerance to crops but the correlation between the expression of induced proteins and the level of stress tolerance has not been explored. In this study, we have reported proteomic changes in different tissues of two chickpea cultivars differing in drought tolerance capacity ICC4958 (drought tolerant) and ILC3279 (drought susceptible) at different developmental stages under field and at 7 days after germination (DAG) under laboratory conditions. An insight into the proteomic changes of these two chickpea cultivars revealed that average polypeptide expression under stress was up regulated and down regulated in underground system of ICC4958 and ILC3279, respectively, as compared to control which affected the protein expression in aboveground tissues. More pronounced increase in polypeptide expression in leaves of ICC4958 under stress was observed at 80 DAS, the stage corresponding to initiation of reproductive development while stress in leaves of ILC3279 resulted in decreased overall protein expression. This was ultimately reflected in enhanced protein expression under water deficit stress in mature seeds of ICC4958 as compared to ILC3279. The study under laboratory condition also revealed that protein expression under water deficit stress is increased on an average in ICC4958 and reduced in ILC3279.

References

Bennett EJ, Roberts JA and Wagstaff C. 2011. The role of the pod in seed development: strategies for manipulating yield. New Phytology 190: 838-853.

Farooq M, Gogoi N, Barthakur S, Baroowa B, Bhardwaj N, Alghamdi SS and KHM Siddique. 2017. Drought stress in grain legumes during reproduction and grain filling. Journal of Agronomy and Crop Science 203: 81-102.

Garg R, Rama S, Bijal T, Himabindu K, Lakshmanan K, Nitin M, Varshney RK and Mukesh SBJ. 2016. Transcriptome analyses reveal genotype-and developmental stage-specific molecular responses to drought and salinity stresses in chickpea. Scientific Reports 6:19228-19228.

Hajheidari M, Abdollahian-Noghabi M, Askari , Heidari M, Sadeghian SY, Ober ES and Hosseini SG. 2005. Proteome analysis of sugarbeet leaves under drought stress. Proteomics 5: 950-960.

Hameed A, Gulzar S, Aziz I, Hussain T, Gul B and Khan MA. 2015. Effects of salinity and ascorbic acid on growth, water status and antioxidant system in a perennial halophyte. AoB Plants:

Hu L, Li H, Pang H and Fu J. 2012. Responses of antioxidant gene, protein and enzymes to salinity stress in two genotypes of perennial ryegrass (Lolium perenne) differing in salt tolerance. Journal of Plant Physiology 169:146-156.

Kakaei M, Kahrizi D and Ebadi AG. 2010. Study of drought response extremes wheat varieties via seed storage constitutive proteins. American Journal of Scientific Research 12: 32-35.

Kreps JA, Wu Y, Chang HS, Zhu T, Wang X and Harper JF. 2002. Transcriptome changes for Arabidopsis in response to salt, osmotic and cold stress. Plant Physiology 130: 2129-2141.

Laemmli UK. 1970. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 227: 680-705.

Oishi MY and Bewley JD. 1992. Premature drying, fluridone treatment, and embryo isolation during development of maize kernels (Zea mays L.) induce germination, but the protein synthetic responses are different. Potential regulation of germination and protein synthesis by abscisic acid. Journal of Experimental Botany 43: 759-767.

Ramamoorthy P, Lakshmanan K, Upadhyayaa HR, Vadez V and Varshneya PK. 2016. Shoot traits and their relevance in terminal drought tolerance of chickpea (Cicer arietinum L.) Field Crops Reserach 197: 10-27.

Sajjo Y, Hata S, Kyozuka, J, Shimamoto K and Izui K. 2000. Over expression of a single Ca2+ dependent protein kinase confers both cold and salt/drought tolerance on rice plants. Plant Journal 23: 319-327.

Samarah NH and Mullen RE. 2006. Total soluble and dehydrin like proteins in full rounded and shriveled seeds of soybean in response to drought stress. Journal of Food, Agriculture and Environment 4: 260-263.

Sengupta D, Kannan M and Reddy AR. 2011. A root proteomics based insight reveals dynamic regulation of root proteins under progressive drought stress and recovery in Vigna radiata (L.) Wilczek. Planta 233: 1111-1127.

Zheng M, Meng Y, Yang C, Zhou Z, Wang Y and Chen B. 2014. Protein expression changes during cotton fiber elongation in response to drought stress and recovery. Proteomics 14:1776-1795.

Zhou S, Palmer M, Zhou J and Bhatti S. 2013. Differential root proteome expression in tomato genotypes with contrasting drought tolerance exposed to dehydration. Journal of the American Society of Horticulture Science 138: 131-141.

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Published

2024-08-03

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How to Cite

Differential organ specific protein profiling in chickpea cultivars under water deficit stress. (2024). Journal of Food Legumes, 31(1), 18-23. https://doi.org/10.59797/journaloffoodlegumes.v31i1.443