Abstract
Wheat, being a staple food grain crop, is highly sensitive to terminal heat stress. The mechanism underlying heat stress tolerance in wheat has yet not been elucidated. Diverse signalling networks has been adopted by the plants in order to regulate their biological functions and protect the cells from the vageries of nature. Out of all the signalling pathways known and characterized, Ca2+ − secondary messenger-linked pathways are very predominant in different biological functions. Calcium Dependent Protein Kinases, showed the presence of N-terminal domain (which is variable), a protein kinase domain (shows phosphorylation activity), an auto-inhibitory region, and a calmodulin-like domain with EF-hand Ca2+-binding sites. CDPKs has been reported to acts as temperature sensing device or thermometer for the plants. It plays very important role in the regulation of guard cells and in ABA-regulated stomatal signalling in Arabidopsis. OsCDPK7 and OsCDPK13 present in rice have been reported to modulate the tolerance level against cold, salt, and drought stresses. CDPKs have also been reported to involved in ROS homeostasis and protection of cells against abiotic stresses. CDPKs has also been observed to modualte the carbon fixation process under adverse conditions. The actual sensory and signalling molecules and/or the primary targets of CPKs mediated regulation of photosynthesis and carbon assimilation metabolism under heat stress are still unclear. It is worthwhile to examine the role of CDPKs in altering the photosynthesis and source-to-sink carbon transfer in wheat under heat stress.
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References
Abbasi F, Onodera H, Toki S et al (2004) OsCDPK13, a calcium-dependent protein kinase gene from rice, is induced by cold and gibberellin in rice leaf sheath. Plant Mol Biol 55:541–552. https://doi.org/10.1007/s11103-004-1178-y
Akter N, Rafiqul Islam M (2017) Heat stress effects and management in wheat. A review Agron Sustain Dev 37:37
Ali S, Hayat K, Iqbal A, Xie L (2020) Implications of abscisic acid in the drought stress tolerance of plants. Agronomy 10
Asano T, Hakata M, Nakamura H et al (2011) Functional characterisation of OsCPK21, a calcium-dependent protein kinase that confers salt tolerance in rice. Plant Mol Biol 75:179–191. https://doi.org/10.1007/s11103-010-9717-1
Asano T, Hayashi N, Kikuchi S, Ohsugi R (2012) CDPK-mediated abiotic stress signaling. Plant Signal Behav 7:817–821
Asseng S (2015) Uncertainties of climate change impacts in agriculture. Procedia Environ Sci 29:304. https://doi.org/10.1016/j.proenv.2015.07.276
Atif RM, Shahid L, Waqas M et al (2019) Insights on calcium-dependent protein kinases (CPKs) signaling for abiotic stress tolerance in plants. Int J Mol Sci 20:5298
Bennett D, Reynolds M, Mullan D et al (2012) Detection of two major grain yield QTL in bread wheat (Triticum aestivum L.) under heat, drought and high yield potential environments. Theor Appl Genet 125(7):1473–1485. https://doi.org/10.1007/s00122-012-1927-2
Brandt B, Munemasa S, Wang C et al (2015) Calcium specificity signaling mechanisms in abscisic acid signal transduction in arabidopsis guard cells. elife 4:e03599. https://doi.org/10.7554/eLife.03599
Chen J, Xue B, Xia X, Yin W et al (2013) A novel calcium-dependent protein kinase gene from Populus euphratica, confers both drought and cold stress tolerance. Biochem Biophys Res Commun 441:630–636. https://doi.org/10.1016/j.bbrc.2013.10.103
Cheng X, Chai L, Chen Z et al (2015) Identification and characterization of a high kernel weight mutant induced by gamma radiation in wheat (Triticum aestivum L.). BMC Genet 16:127. https://doi.org/10.1186/s12863-015-0285-x
Crizel RL, Perin EC, Vighi IL et al (2020) Genome-wide identification, and characterization of the CDPK gene family reveal their involvement in abiotic stress response in Fragaria x ananassa. Sci Rep 10. https://doi.org/10.1038/s41598-020-67957-9
Dahuja A, Kumar RR, Sakhare A et al (2020) Role of ATP-binding cassette transporters in maintaining plant homeostasis under abiotic and biotic stresses. Physiol Plant. https://doi.org/10.1111/ppl.13302
Das R, Pandey G (2009) Expressional analysis and role of calcium regulated kinases in abiotic stress signaling, Curr Genomics 11. https://doi.org/10.2174/138920210790217981
Demidchik V, Shabala S (2018) Mechanisms of cytosolic calcium elevation in plants: The role of ion channels, calcium extrusion systems and NADPH oxidase-mediated “ROS-Ca2+ Hub.” In: Functional Plant Biology
Dong H, Wu C, Luo C, Wei M, Qu S, Wang S (2020) Overexpression of MdCPK1a gene, a calcium dependent protein kinase in apple, increase tobacco cold tolerance via scavenging ROS accumulation. PLoS One 15(11):e0242139
Dubrovina AS, Kiselev KV (2019) The role of calcium-dependent protein kinase genes VaCPK1 and VaCPK26 in the response of Vitis amurensis (in vitro) and Arabidopsis thaliana (in vivo) to abiotic stresses. Russ J Genet 55. https://doi.org/10.1134/S1022795419030049
Geiger D, Scherzer S, Mumm P et al (2009) Activity of guard cell anion channel SLAC1 is controlled by drought-stress signaling kinase-phosphatase pair. Proc Natl Acad Sci U S A 106. https://doi.org/10.1073/pnas.0912021106
Guerrini L, Napoli M, Mancini M et al (2020) Wheat grain composition, dough rheology and bread quality as affected by nitrogen and sulfur fertilization and seeding density. Agronomy 10. https://doi.org/10.3390/agronomy10020233
Hamel LP, Sheen J, Séguin A (2014) Ancient signals: comparative genomics of green plant CDPKs. Trends Plant Sci 19(2):79–89. https://doi.org/10.1016/j.tplants.2013.10.009
He Y, Lin YL, Chen C et al (2019) Impacts of starch and the interactions between starch and other macromolecules on wheat falling number. Compr Rev Food Sci Food Saf 18
Hosseini SZ, Ismaili A, Nazarian-Firouzabadi F et al (2021) Dissecting the molecular responses of lentil to individual and combined drought and heat stresses by comparative transcriptomic analysis. Genomics 113. https://doi.org/10.1016/j.ygeno.2020.12.038
Hu Z, Lv X, Xia X et al (2016) Genome-wide identification and expression analysis of calcium-dependent protein kinase in tomato. Front Plant Sci 7. https://doi.org/10.3389/fpls.2016.00469
Kasajima I (2017) Difference in oxidative stress tolerance between rice cultivars estimated with chlorophyll fluorescence analysis. BMC Res Notes 10. https://doi.org/10.1186/s13104-017-2489-9
Khan I, Gratz R, Denezhkin P et al (2019) Calcium-promoted interaction between the C2-domain protein EHB1 and metal transporter IRT1 inhibits arabidopsis iron acquisition. Plant Physiol 180. https://doi.org/10.1104/pp.19.00163
Kiba T, Inaba J, Kudo T et al (2018) Repression of nitrogen starvation responses by members of the arabidopsis GARP-type transcription factor NIGT1/HRS1 subfamily. Plant Cell 30. https://doi.org/10.1105/tpc.17.00810
Kumar RR, Goswami S, Rai GK et al (2020) Protection from terminal heat stress: a trade-off between heat-responsive transcription factors (HSFs) and stress-associated genes (SAGs) under changing environment. Cereal Res Commun. https://doi.org/10.1007/s42976-020-00097-y
Kumar RR, Goswami S, Singh K et al (2016) Identification of putative RuBisCo Activase (TaRca1)—the catalytic chaperone regulating carbon assimilatory pathway in wheat (Triticum aestivum) under the heat stress. Front Plant Sci 7:986. https://doi.org/10.3389/fpls.2016.00986
Kumar RR, Rai RD (2014) Can wheat beat the heat: understanding the mechanism of Thermotolerance in wheat (Triticum aestivum L.). Cereal Res Commun 42:1–18. https://doi.org/10.1556/CRC.42.2014.1.1
Kumar RR, Singh GP, Goswami S et al (2014) Proteome analysis of wheat ('Triticum aestivum’) for the identification of differentially expressed heat-responsive proteins. Aus J Crop Sci 8:973
Kumar RR, Singh K, Ahuja S et al (2019) Quantitative proteomic analysis reveals novel stress-associated active proteins (SAAPs) and pathways involved in modulating tolerance of wheat under terminal heat. Funct Integr Genomics 19:329–348. https://doi.org/10.1007/s10142-018-0648-2
Li ZY, Xu ZS, Chen Y et al (2013) A novel role for Arabidopsis CBL1 in affecting plant responses to glucose and gibberellin during germination and seedling development. PLoS One 8:e56412. https://doi.org/10.1371/journal.pone.0056412
Li LB, Yu DW, Zhao FL, Pang CY, Song MZ, Wei HL, Fan SL, Yu SX (2015) Genome-wide analysis of the calcium-dependent protein kinase gene family in Gossypium raimondii. J Integr Agric 14(1):29–41
Ma SY, Wu WH (2007) AtCPK23 functions in Arabidopsis responses to drought and salt stresses. Plant Mol Biol 65(4):511–518
Mittler R, Vanderauwera S, Gollery M, Van Breusegem F (2004) Reactive oxygen gene network of plants. Trends Plant Sci 9(10):490–498
Munemasa S, Hauser F, Park J et al (2015) Mechanisms of abscisic acid-mediated control of stomatal aperture. Curr Opin Plant Biol 28:154–162
Ray S, Agarwal P, Arora R, Kapoor S, Tyagi AK (2007) Expression analysis of calcium-dependent protein kinase gene family during reproductive development and abiotic stress conditions in rice (Oryza sativa L. ssp. indica). Mol Gen Genomics 278(5):493–505. https://doi.org/10.1007/s00438-007-0267-4
Raza A, Razzaq A, Mehmood SS et al (2019) Impact of climate change on crops adaptation and strategies to tackle its outcome: a review. Plan Theory 8
Regmi KC, Yogendra K, Farias JG et al (2020) Improved yield and Photosynthate partitioning in AVP1 expressing wheat (Triticum aestivum) plants. Front Plant Sci 11. https://doi.org/10.3389/fpls.2020.00273
Saito S, Uozumi N (2020) Calcium-regulated phosphorylation systems controlling uptake and balance of plant nutrients. Front Plant Sci 11
Sandmann M, Skłodowski K, Gajdanowicz P et al (2011) The K+ battery-regulating Arabidopsis K+ channel AKT2 s under the control of multiple post-translational steps. Plant Signal Behav 6. https://doi.org/10.4161/psb.6.4.14908
Schulze S, Dubeaux G, Ceciliato PHO et al (2021) A role for calcium-dependent protein kinases in differential CO2- and ABA-controlled stomatal closing and low CO2-induced stomatal opening in Arabidopsis. New Phytol 229. https://doi.org/10.1111/nph.17079
Shah WH, Rasool A, Saleem S et al (2021) Understanding the integrated pathways and mechanisms of transporters, protein kinases, and transcription factors in plants under salt stress. Int J Genomics 2021
Shi S, Li S, Asim M et al (2018) The arabidopsis calcium-dependent protein kinases (CDPKs) and their roles in plant growth regulation and abiotic stress responses. Int J Mol Sci 19:1900
Shirdelmoghanloo H, Cozzolino D, Lohraseb I, Collins NC (2016) Truncation of grain filling in wheat (Triticum aestivum) triggered by brief heat stress during early grain filling: association with senescence responses and reductions in stem reserves. Funct Plant Biol 43:919–930. https://doi.org/10.1071/FP15384
Shu B, Jue D, Zhang F, Zhang D, Liu C, Wu Q, Luo C (2020) Genome-wide identification and expression analysis of the citrus calcium-dependent protein kinase (CDPK) genes in response to arbuscular mycorrhizal fungi colonization and drought. Biotechnol Biotechnol Equip 34(1):1304–1314
Simeunovic A, Mair A, Wurzinger B, Teige M (2016) Know where your clients are: subcellular localization and targets of calcium-dependent protein kinases. J Exp Bot 67(13):3855–3872. https://doi.org/10.1093/jxb/erw157
Slattery RA, Ort DR (2019) Carbon assimilation in crops at high temperatures. Plant Cell Environ 42:2750–2758
Song P, Jia Q, Xiao X et al (2021) Hsp70-3 interacts with phospholipase dd and participates in heat stress defense. Plant Physiol 185:1148–1165. https://doi.org/10.1093/PLPHYS/KIAA083
Tang RJ, Luan S (2017) Regulation of calcium and magnesium homeostasis in plants: from transporters to signaling network. Curr Opin Plant Biol 39:97–105
van Es SW (2020) Too hot to handle, the adverse effect of heat stress on crop yield. Physiol Plant 169:499–500. https://doi.org/10.1111/ppl.13165
Vivek PJ, Tuteja N, Soniya EV (2013) CDPK1 from ginger promotes salinity and drought stress tolerance without yield penalty by improving growth and photosynthesis in Nicotiana tabacum. PLoS One 8(10):e76392
Wang L, Yu C, Xu S et al (2016) OsDi19-4 acts downstream of OsCDPK14 to positively regulate ABA response in rice. Plant Cell Environ 39:2740–2753. https://doi.org/10.1111/pce.12829
Wang M, Li Q, Sun K et al (2018) Involvement of CsCDPK20 and CsCDPK26 in regulation of Thermotolerance in tea plant (Camellia sinensis). Plant Mol Biol Report 36:1–12. https://doi.org/10.1007/s11105-018-1068-0
Wei S, Hu W, Deng X et al (2014) A rice calcium-dependent protein kinase OsCPK9 positively regulates drought stress tolerance and spikelet fertility. BMC Plant Biol 14:133. https://doi.org/10.1186/1471-2229-14-133
Wei X, Shen F, Hong Y et al (2016) The wheat calcium-dependent protein kinase TaCPK7-D positively regulates host resistance to sharp eyespot disease. Mol Plant Pathol 17:1252–1264. https://doi.org/10.1111/mpp.12360
Wen F, Ye F, Xiao Z et al (2020) Genome-wide survey and expression analysis of calcium-dependent protein kinase (CDPK) in grass Brachypodium distachyon. BMC Genomics 21:53. https://doi.org/10.1186/s12864-020-6475-6
Xiao XH, Yang M, Sui JL et al (2017) The calcium-dependent protein kinase (CDPK) and CDPK-related kinase gene families in Hevea brasiliensis–comparison with five other plant species in structure, evolution, and expression. FEBS Open Bio 7(1):4–24. https://doi.org/10.1002/2211-5463.12163
Xu J, Tian YS, Peng RH, Xiong AS, Zhu B, Jin XF, Gao F, Fu XY, Hou XL, Yao QH (2010) AtCPK6, a functionally redundant and positive regulator involved in salt/drought stress tolerance in Arabidopsis. Planta 231(6):1251–1260
Yin X, Wang X, Komatsu S (2017) Phosphoproteomics: protein phosphorylation in regulation of seed germination and plant growth. Curr Protein Pept Sci 19:401–412. https://doi.org/10.2174/1389203718666170209151048
Yip Delormel T, Boudsocq M (2019) Properties and functions of calcium-dependent protein kinases and their relatives in Arabidopsis thaliana. New Phytol 224
Zhang X, Högy P, Wu X et al (2018) Physiological and proteomic evidence for the interactive effects of post-Anthesis heat stress and elevated CO2 on wheat. Proteomics 18:e1800262. https://doi.org/10.1002/pmic.201800262
Zhao Y, Du H, Wang Y et al (2021) The calcium-dependent protein kinase ZmCDPK7 functions in heat-stress tolerance in maize. J Integr Plant Biol 63:510–527. https://doi.org/10.1111/jipb.13056
Zhu SY, Yu XC, Wang XJ, Zhao R, Li Y, Fan RC, Shang Y, Du SY, Wang XF, Wu FQ, Xu YH (2007) Two calcium-dependent protein kinases, CPK4 and CPK11, regulate abscisic acid signal transduction in Arabidopsis. Plant Cell 19:3019–3036
Zou JJ, Li XD, Ratnasekera D et al (2015) Arabidopsis calcium-dependent protein kinase8 and CATALASE3 function in abscisic acid-mediated signaling and H2O2 homeostasis in stomatal guard cells under drought stress. Plant Cell 27:1445–1460. https://doi.org/10.1105/tpc.15.00144
Zou JJ, Wei FJ, Wang C et al (2010) Arabidopsis calcium-dependent protein kinase cpk10 functions in abscisic acid- and Ca2+−mediated stomatal regulation in response to drought stress. Plant Physiol 154:1232–1243. https://doi.org/10.1104/pp.110.157545
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Kumar, R.R., Sareen, S., Padaria, J.C., Singh, B., Praveen, S. (2022). CDPKs Based Signalling Network: Protecting the Wheat from Heat. In: Kumar, R.R., Praveen, S., Rai, G.K. (eds) Thermotolerance in Crop Plants. Springer, Singapore. https://doi.org/10.1007/978-981-19-3800-9_7
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