{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,28]],"date-time":"2026-09-28T21:59:59Z","timestamp":1790632799947,"version":"4.1.0"},"reference-count":219,"publisher":"MDPI AG","issue":"5","license":[{"start":{"date-parts":[[2022,5,8]],"date-time":"2022-05-08T00:00:00Z","timestamp":1651968000000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0\/"}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Biomolecules"],"abstract":"<jats:p>Plants encounter several abiotic stresses, among which heat stress is gaining paramount attention because of the changing climatic conditions. Severe heat stress conspicuously reduces crop productivity through changes in metabolic processes and in growth and development. Ethylene and hydrogen sulfide (H2S) are signaling molecules involved in defense against heat stress through modulation of biomolecule synthesis, the antioxidant system, and post-translational modifications. Other compounds containing the essential mineral nutrient sulfur (S) also play pivotal roles in these defense mechanisms. As biosynthesis of ethylene and H2S is connected to the S-assimilation pathway, it is logical to consider the existence of a functional interplay between ethylene, H2S, and S in relation to heat stress tolerance. The present review focuses on the crosstalk between ethylene, H2S, and S to highlight their joint involvement in heat stress tolerance.<\/jats:p>","DOI":"10.3390\/biom12050678","type":"journal-article","created":{"date-parts":[[2022,5,8]],"date-time":"2022-05-08T08:04:21Z","timestamp":1651997061000},"page":"678","update-policy":"https:\/\/doi.org\/10.3390\/mdpi_crossmark_policy","source":"Crossref","is-referenced-by-count":33,"title":["The Functional Interplay between Ethylene, Hydrogen Sulfide, and Sulfur in Plant Heat Stress Tolerance"],"prefix":"10.3390","volume":"12","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-8570-5947","authenticated-orcid":false,"given":"Zebus","family":"Sehar","sequence":"first","affiliation":[{"name":"Plant Physiology and Biochemistry Laboratory, Department of Botany, Aligarh Muslim University, Aligarh 202002, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-4476-5676","authenticated-orcid":false,"given":"Harsha","family":"Gautam","sequence":"additional","affiliation":[{"name":"Plant Physiology and Biochemistry Laboratory, Department of Botany, Aligarh Muslim University, Aligarh 202002, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-6691-496X","authenticated-orcid":false,"given":"Noushina","family":"Iqbal","sequence":"additional","affiliation":[{"name":"Department of Botany, Jamia Hamdard, New Delhi 110062, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ameena Fatima","family":"Alvi","sequence":"additional","affiliation":[{"name":"Plant Physiology and Biochemistry Laboratory, Department of Botany, Aligarh Muslim University, Aligarh 202002, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Badar","family":"Jahan","sequence":"additional","affiliation":[{"name":"Plant Physiology and Biochemistry Laboratory, Department of Botany, Aligarh Muslim University, Aligarh 202002, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-4569-2082","authenticated-orcid":false,"given":"Mehar","family":"Fatma","sequence":"additional","affiliation":[{"name":"Plant Physiology and Biochemistry Laboratory, Department of Botany, Aligarh Muslim University, Aligarh 202002, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-0586-3350","authenticated-orcid":false,"given":"Mohammed","family":"Albaqami","sequence":"additional","affiliation":[{"name":"Department of Biology, Faculty of Applied Science, Umm Al-Qura University, Makkah 21955, Saudi Arabia"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-7957-5832","authenticated-orcid":false,"given":"Nafees A.","family":"Khan","sequence":"additional","affiliation":[{"name":"Plant Physiology and Biochemistry Laboratory, Department of Botany, Aligarh Muslim University, Aligarh 202002, India"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"1968","published-online":{"date-parts":[[2022,5,8]]},"reference":[{"key":"ref_1","doi-asserted-by":"crossref","first-page":"206","DOI":"10.1016\/j.pbi.2009.12.012","article-title":"Dissection and modelling of abiotic stress tolerance in plants","volume":"13","author":"Tardieu","year":"2010","journal-title":"Curr. Opin. Plant Biol."},{"key":"ref_2","first-page":"77","article-title":"The different impact on the growth of cool season turf grass under the various conditions on salinity and draught stress","volume":"3","author":"Saud","year":"2013","journal-title":"Int. J. Agric. Sci. Res."},{"key":"ref_3","doi-asserted-by":"crossref","first-page":"240","DOI":"10.1126\/science.1164363","article-title":"Historical warnings of future food insecurity with unprecedented seasonal heat","volume":"323","author":"Battisti","year":"2009","journal-title":"Science"},{"key":"ref_4","unstructured":"IPCC (2021). The Climate Change 2021: The Physical Science Basis. Contribution of Working Group I to the Sixth Assessment Report of the Intergovernmental Panel on Climate Change, Cambridge University Press."},{"key":"ref_5","first-page":"592","article-title":"Global climate change increases risk of crop yield losses and food insecurity in the tropical Andes","volume":"24","author":"Tito","year":"2014","journal-title":"Glob. Change Biol."},{"key":"ref_6","doi-asserted-by":"crossref","first-page":"5045","DOI":"10.1007\/s10668-019-00414-4","article-title":"Climate change and agriculture in South Asia: Adaptation options in smallholder production systems","volume":"22","author":"Aryal","year":"2020","journal-title":"Environ. Dev. Sustain."},{"key":"ref_7","doi-asserted-by":"crossref","first-page":"53","DOI":"10.1016\/j.gloenvcha.2003.10.008","article-title":"Effect of climate change on global food production under SRES emissions and socio-economic scenarios","volume":"14","author":"Parry","year":"2004","journal-title":"Glob. Environ. Chang."},{"key":"ref_8","doi-asserted-by":"crossref","first-page":"46","DOI":"10.1016\/j.agee.2008.01.019","article-title":"Climate change: Can wheat beat the heat?","volume":"126","author":"Ortiz","year":"2008","journal-title":"Agricul. Ecosyst. Environ."},{"key":"ref_9","doi-asserted-by":"crossref","first-page":"199","DOI":"10.1016\/j.envexpbot.2007.05.011","article-title":"Heat tolerance in plants: An overview","volume":"61","author":"Wahid","year":"2007","journal-title":"Environ. Exp. Bot."},{"key":"ref_10","first-page":"202","article-title":"Protective mechanisms of heat tolerance in crop plants","volume":"10","author":"Asthir","year":"2015","journal-title":"J. Plant Inter."},{"key":"ref_11","doi-asserted-by":"crossref","unstructured":"Hemmati, H., Gupta, D., and Basu, C. (2015). Molecular physiology of heat stress responses in plants. Elucidation of Abiotic Stress Signaling in Plants, Springer.","DOI":"10.1007\/978-1-4939-2540-7_5"},{"key":"ref_12","doi-asserted-by":"crossref","first-page":"467","DOI":"10.1007\/s12192-016-0673-9","article-title":"The effect of heat stress on gene expression, synthesis of steroids, and apoptosis in bovine granulosa cells","volume":"21","author":"Li","year":"2016","journal-title":"Cell Stress Chaperones"},{"key":"ref_13","doi-asserted-by":"crossref","unstructured":"Fatma, M., Iqbal, N., Sehar, Z., Alyemeni, M.N., Kaushik, P., Khan, N.A., and Ahmad, P. (2021). Methyl jasmonate protects the ps ii system by maintaining the stability of chloroplast d1 protein and accelerating enzymatic antioxidants in heat-stressed wheat plants. Antioxidants, 10.","DOI":"10.3390\/antiox10081216"},{"key":"ref_14","doi-asserted-by":"crossref","unstructured":"Iqbal, N., Sehar, Z., Fatma, M., Umar, S., Sofo, A., and Khan, N.A. (2022). Nitric Oxide and Abscisic Acid Mediate Heat Stress Tolerance through Regulation of Osmolytes and Antioxidants to Protect Photosynthesis and Growth in Wheat Plants. Antioxidants, 11.","DOI":"10.3390\/antiox11020372"},{"key":"ref_15","doi-asserted-by":"crossref","unstructured":"Ashraf, M., and Harris, P.J.C. (2005). Genetic improvements of tolerance to high temperature. Abiotic Stresses\u2013Plant Resistance through Breeding and Molecular Approaches, Haworth Press Inc.","DOI":"10.1201\/9781482293609-18"},{"key":"ref_16","doi-asserted-by":"crossref","unstructured":"Shinozaki, K., and Yamaguchi-Shinozaki, K. (1999). Molecular responses to heat stress. Molecular Responses to Cold, Drought, Heat and Salt Stress in Higher Plants, R.G. Landes Co.","DOI":"10.1016\/B978-0-444-82884-2.50013-3"},{"key":"ref_17","doi-asserted-by":"crossref","unstructured":"Bhattacharya, A. (2019). Effect of High Temperature on Crop Productivity and Metabolism of Macro Molecules, Academic Press. [1st ed.].","DOI":"10.1016\/B978-0-12-817562-0.00001-X"},{"key":"ref_18","doi-asserted-by":"crossref","first-page":"11","DOI":"10.1111\/j.1365-3040.2007.01727.x","article-title":"The effect of drought and heat stress on reproductive processes in cereals","volume":"31","year":"2008","journal-title":"Plant Cell Environ."},{"key":"ref_19","doi-asserted-by":"crossref","first-page":"717","DOI":"10.1111\/j.1365-3040.2004.01171.x","article-title":"Electron transport is the functional limitation of photosynthesis in field-grown Pima cotton plants at high temperature","volume":"27","author":"Wise","year":"2004","journal-title":"Plant Cell Environ."},{"key":"ref_20","doi-asserted-by":"crossref","unstructured":"Gautam, H., Sehar, Z., Rehman, M.T., Hussain, A., AlAjmi, M.F., and Khan, N.A. (2021). Nitric oxide enhances photosynthetic nitrogen and sulfur-use efficiency and activity of ascorbate-glutathione cycle to reduce high temperature stress-induced oxidative stress in rice (Oryza sativa L.) plants. Biomolecules, 11.","DOI":"10.3390\/biom11020305"},{"key":"ref_21","first-page":"203","article-title":"High-temperature preconditioning and thermal shock imposition affects water relations, gas exchange and root hydraulic conductivity in tomato","volume":"47","author":"Morales","year":"2019","journal-title":"Biol. Plantar."},{"key":"ref_22","doi-asserted-by":"crossref","first-page":"942","DOI":"10.1093\/mp\/ssq044","article-title":"Sugar input, metabolism, and signaling mediated by invertase: Roles in development, yield potential, and response to drought and heat","volume":"3","author":"Ruan","year":"2010","journal-title":"Mol. Plant"},{"key":"ref_23","doi-asserted-by":"crossref","first-page":"177","DOI":"10.1071\/FP05067","article-title":"Changes in photosynthetic parameters and antioxidant activities following heat-shock treatment in tomato plants","volume":"33","author":"Camejo","year":"2006","journal-title":"Funct. Plant Biol."},{"key":"ref_24","doi-asserted-by":"crossref","first-page":"e26374","DOI":"10.4161\/psb.26374","article-title":"Salicylic acid alleviates adverse effects of heat stress on photosynthesis through changes in proline production and ethylene formation","volume":"8","author":"Khan","year":"2013","journal-title":"Plant Signal. Behav."},{"key":"ref_25","doi-asserted-by":"crossref","unstructured":"Gautam, H., Fatma, M., Sehar, Z., Iqbal, N., Albaqami, M., and Khan, N.A. (2022). Exogenously-Sourced Ethylene Positively Modulates Photosynthesis, Carbohydrate Metabolism, and Antioxidant Defense to Enhance Heat Tolerance in Rice. Int. J. Mol. Sci., 23.","DOI":"10.3390\/ijms23031031"},{"key":"ref_26","doi-asserted-by":"crossref","first-page":"179","DOI":"10.1016\/S1360-1385(03)00047-5","article-title":"Acquired tolerance to temperature extremes","volume":"8","author":"Sung","year":"2003","journal-title":"Trends Plant Sci."},{"key":"ref_27","doi-asserted-by":"crossref","first-page":"165","DOI":"10.1016\/j.envexpbot.2017.05.002","article-title":"Physiological and biochemical responses to high light and temperature stress in plants","volume":"139","author":"Orzechowska","year":"2017","journal-title":"Environ. Exp. Bot."},{"key":"ref_28","doi-asserted-by":"crossref","first-page":"9643","DOI":"10.3390\/ijms14059643","article-title":"Physiological, biochemical, and molecular mechanisms of heat stress tolerance in plants","volume":"14","author":"Hasanuzzaman","year":"2013","journal-title":"Int. J. Mol. Sci."},{"key":"ref_29","doi-asserted-by":"crossref","first-page":"1582","DOI":"10.3389\/fpls.2017.01582","article-title":"Nitric oxide (NO) in plant heat stress tolerance: Current knowledge and perspectives","volume":"8","author":"Parankusam","year":"2017","journal-title":"Front. Plant Sci."},{"key":"ref_30","doi-asserted-by":"crossref","first-page":"541","DOI":"10.1007\/s11120-008-9331-0","article-title":"Heat stress: An overview of molecular responses in photosynthesis","volume":"98","author":"Allakhverdiev","year":"2008","journal-title":"Photosynth. Res."},{"key":"ref_31","doi-asserted-by":"crossref","first-page":"3027","DOI":"10.1104\/pp.17.01672","article-title":"Plastid translation elongation factor Tu is prone to heat-induced aggregation despite its critical role in plant heat tolerance","volume":"176","author":"Li","year":"2018","journal-title":"Plant Physiol."},{"key":"ref_32","doi-asserted-by":"crossref","unstructured":"Wani, S.H., and Kumar, V. (2020). Alteration in Carbohydrate Metabolism Modulates Thermotolerance of Plant under Heat Stress. Heat Stress Tolerance in Plants: Physiological, Molecular and Genetic Perspectives, John Wiley & Sons Ltd.. [1st ed.].","DOI":"10.1002\/9781119432401"},{"key":"ref_33","doi-asserted-by":"crossref","first-page":"1178","DOI":"10.1093\/treephys\/tpaa069","article-title":"Effect of summer warming on growth, photosynthesis and water status in female and male Populus cathayana: Implications for sex-specific drought and heat tolerances","volume":"40","author":"Liu","year":"2020","journal-title":"Tree Physiol."},{"key":"ref_34","doi-asserted-by":"crossref","unstructured":"Wang, L., Ma, K.B., Lu, Z.G., Ren, S.X., Jiang, H.R., Cui, J.W., Chen, G., Teng, N.J., Lam, H.M., and Jin, B. (2020). Differential physiological, transcriptomic and metabolomic responses of Arabidopsis leaves under prolonged warming and heat shock. BMC Plant Biol., 20.","DOI":"10.1186\/s12870-020-2292-y"},{"key":"ref_35","doi-asserted-by":"crossref","first-page":"513","DOI":"10.3109\/02656736.2014.971446","article-title":"Reactive oxygen species, heat stress and oxidative-induced mitochondrial damage. A review","volume":"30","author":"Slimen","year":"2014","journal-title":"Int. J. Hyperthermia."},{"key":"ref_36","doi-asserted-by":"crossref","unstructured":"Zhao, J., Lu, Z., Wang, L., and Jin, B. (2021). Plant Responses to Heat Stress: Physiology, Transcription, Noncoding RNAs, and Epigenetics. Int. J. Mol. Sci., 22.","DOI":"10.3390\/ijms22010117"},{"key":"ref_37","doi-asserted-by":"crossref","first-page":"736","DOI":"10.1111\/ppl.12997","article-title":"Systematic identification and analysis of heat-stress-responsive lncRNAs, circRNAs and miRNAs with associated co-expression and ceRNA networks in cucumber (Cucumis sativus L.)","volume":"168","author":"He","year":"2020","journal-title":"Physiol. Plant."},{"key":"ref_38","doi-asserted-by":"crossref","first-page":"1419","DOI":"10.1016\/j.ygeno.2019.08.011","article-title":"Non-coding RNAs: Functional roles in the regulation of stress response in Brassica crops","volume":"112","author":"Ahmed","year":"2020","journal-title":"Genomics"},{"key":"ref_39","doi-asserted-by":"crossref","first-page":"66","DOI":"10.1093\/plphys\/kiac049","article-title":"A long non-coding RNA functions in high-light-induced anthocyanin accumulation in apple by activating ethylene synthesis","volume":"189","author":"Yu","year":"2022","journal-title":"Plant Physiol."},{"key":"ref_40","doi-asserted-by":"crossref","first-page":"151","DOI":"10.1016\/j.gene.2018.06.089","article-title":"Analysis of long-non-coding RNAs associated with ethylene in tomato","volume":"674","author":"Wang","year":"2018","journal-title":"Gene"},{"key":"ref_41","unstructured":"Singh, S., Singh, V., Tripathi, D., Prasad, S., Chauhan, D., and Dubey, N.K. (2021). Gene regulation by H2S in plants. Hydrogen Sulfide in Plant Biology, Elsevier."},{"key":"ref_42","doi-asserted-by":"crossref","first-page":"225","DOI":"10.1146\/annurev.arplant.53.100201.160729","article-title":"Acclimative response to temperature stress in higher plants: Approaches of gene engineering for temperature tolerance","volume":"53","author":"Iba","year":"2002","journal-title":"Ann. Rev. Plant Biol."},{"key":"ref_43","first-page":"2318","article-title":"Plant Hormone-Mediated Regulation of Heat Tolerance in Response to Global Climate Change","volume":"11","author":"Li","year":"2020","journal-title":"Front. Plant Sci."},{"key":"ref_44","doi-asserted-by":"crossref","first-page":"175","DOI":"10.1111\/j.1469-8137.2008.02735.x","article-title":"Jasmonates act with salicylic acid to confer basal thermotolerance in Arabidopsis thaliana","volume":"182","author":"Clarke","year":"2009","journal-title":"New Phytol."},{"key":"ref_45","doi-asserted-by":"crossref","first-page":"225","DOI":"10.1007\/s10725-009-9436-2","article-title":"Heat shock protein 70 regulates the abscisic acid-induced antioxidant response of maize to combined drought and heat stress","volume":"60","author":"Hu","year":"2010","journal-title":"Plant Growth Regul."},{"key":"ref_46","first-page":"675","article-title":"Ethylene involvement in the regulation of heat stress tolerance in plants","volume":"41","author":"Nawaz","year":"2021","journal-title":"Plant Cell Rep."},{"key":"ref_47","doi-asserted-by":"crossref","first-page":"pls024","DOI":"10.1093\/aobpla\/pls024","article-title":"Ethylene is involved in maintaining tomato (Solanum lycopersicum) pollen quality under heat-stress conditions","volume":"2012","author":"Firon","year":"2012","journal-title":"AoB Plants"},{"key":"ref_48","doi-asserted-by":"crossref","first-page":"110733","DOI":"10.1016\/j.plantsci.2020.110733","article-title":"Hydrogen sulfide: Roles in plant abiotic stress response and crosstalk with other signals","volume":"302","author":"Huang","year":"2021","journal-title":"Plant Sci."},{"key":"ref_49","doi-asserted-by":"crossref","first-page":"e1477905","DOI":"10.1080\/15592324.2018.1477905","article-title":"Interaction of sulfur with phytohormones and signaling molecules in conferring abiotic stress tolerance to plants","volume":"13","author":"Hasanuzzaman","year":"2018","journal-title":"Plant Signal. Behav."},{"key":"ref_50","doi-asserted-by":"crossref","first-page":"60","DOI":"10.1007\/s12042-015-9152-1","article-title":"Sulfur metabolism and stress defense responses in plants","volume":"8","author":"Capaldi","year":"2015","journal-title":"Trop. Plant Biol."},{"key":"ref_51","doi-asserted-by":"crossref","first-page":"67","DOI":"10.1016\/j.plaphy.2014.03.026","article-title":"Alleviation of salt-induced photosynthesis and growth inhibition by salicylic acid involves glycinebetaine and ethylene in mungbean (Vigna radiata L.)","volume":"80","author":"Khan","year":"2014","journal-title":"Plant Physiol. Biochem."},{"key":"ref_52","doi-asserted-by":"crossref","unstructured":"Khan, N.A., Singh, S., and Umar, S. (2008). Response of photosynthetic organelles to abiotic stress: Modulation by sulfur metabolism. Sulfur Assimilation and Abiotic Stress in Plants, Springer.","DOI":"10.1007\/978-3-540-76326-0"},{"key":"ref_53","doi-asserted-by":"crossref","unstructured":"Rather, B.A., Mir, I.R., Masood, A., Anjum, N.A., and Khan, N.A. (2022). Ethylene-nitrogen synergism induces tolerance to copper stress by modulating antioxidant system and nitrogen metabolism and improves photosynthetic capacity in mustard. Environ. Sci. Poll. Res., 1\u201321.","DOI":"10.1007\/s11356-022-19380-y"},{"key":"ref_54","doi-asserted-by":"crossref","first-page":"288","DOI":"10.1080\/03650340.2016.1196811","article-title":"Significance of sulfur in heat stressed cluster bean (Cymopsis tetragonoloba L. Taub) genotypes, responses of growth, sugar and antioxidative metabolism","volume":"63","author":"Mobin","year":"2017","journal-title":"Arch. Agron. Soil Sci."},{"key":"ref_55","doi-asserted-by":"crossref","first-page":"1249","DOI":"10.1111\/1567-1364.12218","article-title":"Thiamine increases the resistance of baker\u2019s yeast Saccharomyces cerevisiae against oxidative, osmotic and thermal stress, through mechanisms partly independent of thiamine diphosphate-bound enzymes","volume":"14","author":"Wolak","year":"2014","journal-title":"FEMS Yeast Res."},{"key":"ref_56","doi-asserted-by":"crossref","first-page":"361","DOI":"10.1093\/aob\/mcl106","article-title":"Proteome profiling of Populus euphratica upon heat stress","volume":"98","author":"Ferreira","year":"2006","journal-title":"Ann. Bot."},{"key":"ref_57","doi-asserted-by":"crossref","first-page":"251","DOI":"10.1111\/j.1399-3054.2010.01432.x","article-title":"Differential metabolic responses of perennial grass Cynodon transvaalensis \u00d7 Cynodon dactylon (C4) and Poa pratensis (C3) to heat stress","volume":"141","author":"Du","year":"2011","journal-title":"Physiol. Plant."},{"key":"ref_58","doi-asserted-by":"crossref","first-page":"439","DOI":"10.1104\/pp.116.1.439","article-title":"The small, methionine-rich chloroplast heat-shock protein protects photosystem II electron transport during heat stress","volume":"116","author":"Heckathorn","year":"1998","journal-title":"Plant Physiol."},{"key":"ref_59","doi-asserted-by":"crossref","first-page":"595","DOI":"10.1007\/s11248-012-9666-3","article-title":"The polyamine spermine protects Arabidopsis from heat stress-induced damage by increasing expression of heat shock-related genes","volume":"22","author":"Sagor","year":"2013","journal-title":"Transgenic Res."},{"key":"ref_60","doi-asserted-by":"crossref","first-page":"454","DOI":"10.1111\/j.1365-3040.2011.02400.x","article-title":"Glutathione in plants: An integrated overview","volume":"35","author":"Noctor","year":"2012","journal-title":"Plant Cell Environ."},{"key":"ref_61","doi-asserted-by":"crossref","first-page":"3729","DOI":"10.1093\/jxb\/ery166","article-title":"Glutathione modulates the expression of heat shock proteins via the transcription factors BZIP10 and MYB21 in Arabidopsis","volume":"69","author":"Kumar","year":"2018","journal-title":"J. Exp. Bot."},{"key":"ref_62","first-page":"2963","article-title":"Glutathione Regulates 1-Aminocyclopropane-1-Carboxylate Synthase Transcription via WRKY33 and 1-Aminocyclopropane-1-Carboxylate Oxidase by Modulating Messenger RNA Stability to Induce Ethylene Synthesis during Stress","volume":"169","author":"Datta","year":"2015","journal-title":"Plant Physiol."},{"key":"ref_63","doi-asserted-by":"crossref","first-page":"284","DOI":"10.1111\/j.1399-3054.2009.01220.x","article-title":"Ethylene and salicylic acid control glutathione biosynthesis in ozone-exposed Arabidopsis thaliana","volume":"136","author":"Yoshida","year":"2009","journal-title":"Physiol. Plant."},{"key":"ref_64","doi-asserted-by":"crossref","first-page":"458","DOI":"10.3389\/fpls.2015.00458","article-title":"Abscisic acid enhances tolerance of wheat seedlings to drought and regulates transcript levels of genes encoding ascorbate-glutathione biosynthesis","volume":"6","author":"Wei","year":"2015","journal-title":"Front. Plant Sci."},{"key":"ref_65","doi-asserted-by":"crossref","first-page":"323","DOI":"10.1093\/mp\/sss105","article-title":"Thioredoxin reductase type C (NTRC) orchestrates enhanced thermotolerance to Arabidopsis by its redox-dependent holdase chaperone function","volume":"6","author":"Chae","year":"2013","journal-title":"Mol. Plant."},{"key":"ref_66","doi-asserted-by":"crossref","first-page":"11607","DOI":"10.3390\/ijms140611607","article-title":"The physiological importance of glucosinolates on plant response to abiotic stress in Brassica","volume":"14","author":"Moreno","year":"2013","journal-title":"Int. J. Mol. Sci."},{"key":"ref_67","doi-asserted-by":"crossref","first-page":"4733","DOI":"10.1093\/jxb\/erx352","article-title":"More than just an intermediate: Hydrogen sulfide signalling in plants","volume":"68","author":"Filipovic","year":"2017","journal-title":"J. Exp. Bot."},{"key":"ref_68","doi-asserted-by":"crossref","first-page":"277","DOI":"10.1111\/jipb.12004","article-title":"Hydrogen sulfide regulates ethylene-induced stomatal closure in Arabidopsis thaliana","volume":"55","author":"Hou","year":"2013","journal-title":"J. Int. Plant Biol."},{"key":"ref_69","doi-asserted-by":"crossref","first-page":"3547","DOI":"10.1007\/s11434-011-4819-y","article-title":"Hydrogen sulfide induced by nitric oxide mediates ethylene-induced stomatal closure of Arabidopsis thaliana","volume":"56","author":"Liu","year":"2011","journal-title":"Chin. Sci. Bull."},{"key":"ref_70","doi-asserted-by":"crossref","unstructured":"Ge, Y., Hu, K.D., Wang, S.S., Hu, L.Y., Chen, X.Y., Li, Y.H., and Zhang, H. (2017). Hydrogen sulfide alleviates postharvest ripening and senescence of banana by antagonizing the effect of ethylene. PLoS ONE, 12.","DOI":"10.1371\/journal.pone.0180113"},{"key":"ref_71","doi-asserted-by":"crossref","unstructured":"Husain, T., Suhel, M., Prasad, S.M., and Singh, V.P. (2021). Ethylene and hydrogen sulphide are essential for mitigating hexavalent chromium stress in two pulse crops. Plant Biol.","DOI":"10.1111\/plb.13324"},{"key":"ref_72","doi-asserted-by":"crossref","first-page":"371","DOI":"10.1007\/s00709-018-1298-x","article-title":"The mechanism of hydrogen sulfide mitigation of iron deficiency-induced chlorosis in strawberry (Fragaria \u00d7 ananassa) plants","volume":"256","author":"Kaya","year":"2019","journal-title":"Protoplasma"},{"key":"ref_73","doi-asserted-by":"crossref","first-page":"207","DOI":"10.1007\/s11240-015-0939-4","article-title":"Hydrogen sulfide partly mediates abscisic acid-induced heat tolerance in tobacco (Nicotiana tabacum L.) suspension cultured cells","volume":"125","author":"Li","year":"2016","journal-title":"Plant Cell Tissue Organ Cult."},{"key":"ref_74","doi-asserted-by":"crossref","first-page":"50","DOI":"10.1016\/j.envexpbot.2018.08.034","article-title":"Hydrogen sulfide and environmental stresses","volume":"161","author":"Hancock","year":"2019","journal-title":"Environ. Exp. Bot."},{"key":"ref_75","doi-asserted-by":"crossref","first-page":"36","DOI":"10.1016\/j.plaphy.2021.02.024","article-title":"The intricacy of silicon, plant growth regulators and other signaling molecules for abiotic stress tolerance: An entrancing crosstalk between stress alleviators","volume":"162","author":"Khan","year":"2021","journal-title":"Plant Physiol. Biochem."},{"key":"ref_76","doi-asserted-by":"crossref","first-page":"367","DOI":"10.17221\/367\/2012-PSE","article-title":"Interactions between nitrogen nutrition and phytohormone levels in Festulolium plants","volume":"58","author":"Neuberg","year":"2012","journal-title":"Plant Soil Environ."},{"key":"ref_77","doi-asserted-by":"crossref","first-page":"54","DOI":"10.1016\/j.ecoenv.2014.04.017","article-title":"Ethylene production is associated with alleviation of cadmium-induced oxidative stress by sulfur in mustard types differing in ethylene sensitivity","volume":"106","author":"Asgher","year":"2014","journal-title":"Ecotoxicol. Environ. Saf."},{"key":"ref_78","doi-asserted-by":"crossref","first-page":"181","DOI":"10.3390\/stresses1030014","article-title":"Coordinated role of nitric oxide, ethylene, nitrogen, and sulfur in plant salt stress tolerance","volume":"1","author":"Jahan","year":"2021","journal-title":"Stresses"},{"key":"ref_79","unstructured":"Khan, M.I.R., Reddy, P.S., Ferrante, A., and Khan, N.A. (2019). Sulfur availability potentiates phytohormones-mediated action in plants. Plant Signaling Molecules, Woodhead Publishing."},{"key":"ref_80","doi-asserted-by":"crossref","unstructured":"Jahan, B., Iqbal, N., Fatma, M., Sehar, Z., Masood, A., Sofo, A., and Khan, N.A. (2021). Ethylene supplementation combined with split application of nitrogen and sulfur protects salt-inhibited photosynthesis through optimization of proline metabolism and antioxidant system in mustard (Brassica juncea L.). Plants, 10.","DOI":"10.20944\/preprints202106.0095.v1"},{"key":"ref_81","doi-asserted-by":"crossref","first-page":"32","DOI":"10.1007\/s42994-021-00035-4","article-title":"Hydrogen sulfide (H2S) signaling in plant development and stress responses","volume":"2","author":"Liu","year":"2021","journal-title":"Abiotech"},{"key":"ref_82","doi-asserted-by":"crossref","first-page":"118221","DOI":"10.1016\/j.envpol.2021.118221","article-title":"Sulfur deficiency exacerbates phytotoxicity and residues of imidacloprid through suppression of thiol-dependent detoxification in lettuce seedlings","volume":"291","author":"Zhang","year":"2021","journal-title":"Environ. Poll."},{"key":"ref_83","doi-asserted-by":"crossref","first-page":"670308","DOI":"10.3389\/fpls.2021.670308","article-title":"Interaction between sulfur and iron in plants","volume":"12","author":"Astolfi","year":"2021","journal-title":"Front. Plant Sci."},{"key":"ref_84","doi-asserted-by":"crossref","first-page":"1392","DOI":"10.1111\/nph.15704","article-title":"Distribution of control in the sulfur assimilation in Arabidopsis thaliana depends on environmental conditions","volume":"222","author":"Veith","year":"2019","journal-title":"New Phytolol."},{"key":"ref_85","first-page":"437","article-title":"Involvement of sulfur in the regulation of abiotic stress tolerance in plants. Protective chemical agents in the amelioration of plant abiotic stress","volume":"11","author":"Samanta","year":"2020","journal-title":"Biochem. Mol. Perspect."},{"key":"ref_86","doi-asserted-by":"crossref","first-page":"1253","DOI":"10.1021\/acs.chemrev.7b00205","article-title":"Chemical biology of H2S signaling through persulfidation","volume":"118","author":"Filipovic","year":"2018","journal-title":"Chem. Rev."},{"key":"ref_87","doi-asserted-by":"crossref","first-page":"2063","DOI":"10.3389\/fpls.2020.545453","article-title":"Role of exogenous and endogenous hydrogen sulfide (H2S) on functional traits of plants under heavy metal stresses: A recent perspective","volume":"11","author":"Arif","year":"2021","journal-title":"Front. Plant Sci."},{"key":"ref_88","doi-asserted-by":"crossref","first-page":"4089","DOI":"10.1093\/jxb\/erz094","article-title":"Structural biology of plant sulfur metabolism: From sulfate to glutathione","volume":"70","author":"Jez","year":"2019","journal-title":"J. Exp. Bot."},{"key":"ref_89","doi-asserted-by":"crossref","first-page":"977","DOI":"10.1111\/j.1469-8137.2010.03465.x","article-title":"Hydrogen sulphide, a novel gasotransmitter involved in guard cell signalling","volume":"188","author":"Lamattina","year":"2010","journal-title":"New Phytol."},{"key":"ref_90","doi-asserted-by":"crossref","first-page":"4251","DOI":"10.1093\/jxb\/erz225","article-title":"Signaling by hydrogen sulfide and cyanide through post-translational modification","volume":"70","author":"Gotor","year":"2019","journal-title":"J. Exp. Bot."},{"key":"ref_91","doi-asserted-by":"crossref","first-page":"523","DOI":"10.1016\/j.plaphy.2020.08.005","article-title":"The outcomes of the functional interplay of nitric oxide and hydrogen sulfide in metal stress tolerance in plants","volume":"155","author":"Rather","year":"2020","journal-title":"Plant Physiol. Biochem."},{"key":"ref_92","doi-asserted-by":"crossref","first-page":"319","DOI":"10.3390\/hydrogen2030017","article-title":"Hydrogen Sulfide: A Robust Combatant against Abiotic Stresses in Plants","volume":"2","author":"Khanna","year":"2021","journal-title":"Hydrogen"},{"key":"ref_93","doi-asserted-by":"crossref","first-page":"1404","DOI":"10.3389\/fpls.2018.01404","article-title":"Central role of adenosine 5\u2032-phosphosulfate reductase in the control of plant hydrogen sulfide metabolism","volume":"9","author":"Fu","year":"2018","journal-title":"Front. Plant Sci."},{"key":"ref_94","doi-asserted-by":"crossref","first-page":"184","DOI":"10.1104\/pp.61.2.184","article-title":"Light-dependent emission of hydrogen sulfide from plants","volume":"61","author":"Wilson","year":"1978","journal-title":"Plant Physiol."},{"key":"ref_95","doi-asserted-by":"crossref","unstructured":"Wang, C., Deng, Y., Liu, Z., and Liao, W. (2021). Hydrogen Sulfide in Plants: Crosstalk with Other Signal Molecules in Response to Abiotic Stresses. Int. J. Mol. Sci., 22.","DOI":"10.3390\/ijms222112068"},{"key":"ref_96","doi-asserted-by":"crossref","first-page":"983","DOI":"10.1016\/j.tplants.2019.08.003","article-title":"Hydrogen sulfide: A new warrior against abiotic stress","volume":"24","author":"Corpas","year":"2019","journal-title":"Trends Plant Sci."},{"key":"ref_97","doi-asserted-by":"crossref","first-page":"1227","DOI":"10.1111\/ppl.13432","article-title":"Hydrogen sulfide: An emerging signaling molecule regulating drought stress response in plants","volume":"172","author":"Thakur","year":"2021","journal-title":"Physiol. Plantar."},{"key":"ref_98","doi-asserted-by":"crossref","first-page":"5","DOI":"10.1016\/j.niox.2013.07.002","article-title":"Hydrogen sulfide chemical biology: Pathophysiological roles and detection","volume":"35","author":"Kolluru","year":"2013","journal-title":"Nitric oxide"},{"key":"ref_99","doi-asserted-by":"crossref","first-page":"205","DOI":"10.1089\/ars.2008.2132","article-title":"A source of hydrogen sulfide and a mechanism of its release in the brain","volume":"11","author":"Ishigami","year":"2009","journal-title":"Antioxid. Redox Signal."},{"key":"ref_100","doi-asserted-by":"crossref","first-page":"243","DOI":"10.1007\/s00726-004-0072-x","article-title":"Endogenous production of hydrogen sulfide in mammals","volume":"26","author":"Kamoun","year":"2004","journal-title":"Amino Acids"},{"key":"ref_101","doi-asserted-by":"crossref","first-page":"2276","DOI":"10.1016\/j.freeradbiomed.2012.04.007","article-title":"Analytical measurement of discrete hydrogen sulfide pools in biological specimens","volume":"52","author":"Shen","year":"2012","journal-title":"Free Radic Biol. Med."},{"key":"ref_102","doi-asserted-by":"crossref","first-page":"104408","DOI":"10.1016\/j.envexpbot.2021.104408","article-title":"Regulation of arsenic stress response by ethylene biosynthesis and signaling in Arabidopsis thaliana","volume":"185","author":"Singh","year":"2021","journal-title":"Environ. Exp. Bot."},{"key":"ref_103","doi-asserted-by":"crossref","first-page":"3235","DOI":"10.1105\/tpc.106.046458","article-title":"Arabidopsis SLIM1 is a central transcriptional regulator of plant sulfur response and metabolism","volume":"18","author":"Nakamura","year":"2006","journal-title":"Plant Cell"},{"key":"ref_104","first-page":"575","article-title":"To control and to be controlled: Understanding the Arabidopsis SLIM1 function in sulfur deficiency through comprehensive investigation of the EIL protein family","volume":"5","author":"Sirko","year":"2014","journal-title":"Front. Plant Sci."},{"key":"ref_105","doi-asserted-by":"crossref","first-page":"1071","DOI":"10.1071\/FP10089","article-title":"Ethylene production under high temperature stress causes premature leaf senescence in soybean","volume":"37","author":"Djanaguiraman","year":"2010","journal-title":"Funct. Plant Biol."},{"key":"ref_106","doi-asserted-by":"crossref","unstructured":"Buck, H.T., Nisi, J.E., and Salom\u00f3n, N. (2007). Expression quantitative trait loci mapping heat tolerance during reproductive development in wheat (Triticum aestivum). Wheat Production in Stressed Environments. Developments in Plant Breeding, Springer.","DOI":"10.1007\/1-4020-5497-1"},{"key":"ref_107","doi-asserted-by":"crossref","first-page":"23","DOI":"10.1186\/s40529-019-0272-z","article-title":"Ethylene-mediated signaling confers thermo-tolerance and regulates transcript levels of heat shock factors in rice seedlings under heat stress","volume":"60","author":"Wu","year":"2019","journal-title":"Bot. Stud."},{"key":"ref_108","doi-asserted-by":"crossref","first-page":"682","DOI":"10.1104\/pp.010320","article-title":"Protection against heat stress-induced oxidative damage in Arabidopsis involves calcium, abscisic acid, ethylene, and salicylic acid","volume":"128","author":"Larkindale","year":"2002","journal-title":"Plant Physiol."},{"key":"ref_109","doi-asserted-by":"crossref","first-page":"1558","DOI":"10.3389\/fpls.2018.01558","article-title":"Proteomics of heat-stress and ethylene-mediated thermotolerance mechanisms in tomato pollen grains","volume":"9","author":"Jegadeesan","year":"2018","journal-title":"Front. Plant Sci."},{"key":"ref_110","doi-asserted-by":"crossref","first-page":"405","DOI":"10.1078\/0176-1617-01239","article-title":"Thermotolerance and antioxidant systems in Agrostis stolonifera: Involvement of salicylic acid, abscisic acid, calcium, hydrogen peroxide, and ethylene","volume":"161","author":"Larkindale","year":"2004","journal-title":"J. Plant Physiol."},{"key":"ref_111","doi-asserted-by":"crossref","first-page":"465","DOI":"10.15258\/sst.2006.34.2.21","article-title":"Ameliorative effects of ethylene precursor and polyamines on the high temperature inhibition of seed germination in lettuce (Lactuca sativa L.) before and after seed storage","volume":"34","author":"Korkmaz","year":"2006","journal-title":"Seed Sci. Technol."},{"key":"ref_112","doi-asserted-by":"crossref","first-page":"167","DOI":"10.15258\/sst.2017.45.1.07","article-title":"Ethylene regulators influence germination and root growth of globe artichoke seedlings exposed to heat stress conditions","volume":"45","author":"Shinohara","year":"2017","journal-title":"Seed Sci. Technol."},{"key":"ref_113","doi-asserted-by":"crossref","first-page":"249","DOI":"10.1007\/s10725-013-9885-5","article-title":"The novel ethylene antagonist, 3-cyclopropyl-1-enyl-propanoic acid sodium salt (CPAS), increases grain yield in wheat by delaying leaf senescence","volume":"73","author":"Huberman","year":"2014","journal-title":"Plant Growth Regul."},{"key":"ref_114","doi-asserted-by":"crossref","first-page":"487","DOI":"10.4236\/ajps.2021.124032","article-title":"An ethylene over-producing mutant of tomato (Solanum lycopersicum), epinastic, exhibits tolerance to high temperature conditions","volume":"12","author":"Jegadeesan","year":"2021","journal-title":"Amer. J. Plant Sci."},{"key":"ref_115","doi-asserted-by":"crossref","first-page":"1486","DOI":"10.1111\/pce.13820","article-title":"Balancing of hormonal biosynthesis and catabolism pathways, a strategy to ameliorate the negative effects of heat stress on reproductive growth","volume":"44","author":"Kaur","year":"2021","journal-title":"Plant Cell Environ."},{"key":"ref_116","doi-asserted-by":"crossref","unstructured":"Jespersen, D., Yu, J., and Huang, B. (2015). Metabolite responses to exogenous application of nitrogen, cytokinin, and ethylene inhibitors in relation to heat-induced senescence in creeping bentgrass. PLoS ONE, 10.","DOI":"10.1371\/journal.pone.0123744"},{"key":"ref_117","doi-asserted-by":"crossref","first-page":"32","DOI":"10.1104\/pp.15.00677","article-title":"Ethylene response factors: A key regulatory hub in hormone and stress signaling","volume":"169","year":"2015","journal-title":"Plant Physiol."},{"key":"ref_118","doi-asserted-by":"crossref","first-page":"1566","DOI":"10.1104\/pp.113.221911","article-title":"The Arabidopsis Ethylene Response Factor1 regulates abiotic stress-responsive gene expression by binding to different cis-acting elements in response to different stress signals","volume":"162","author":"Cheng","year":"2013","journal-title":"Plant Physiol."},{"key":"ref_119","first-page":"100632","article-title":"Transcriptome analysis and weighted gene co-expression network reveals potential genes responses to heat stress in turbot Scophthalmus maximus","volume":"33","author":"Huang","year":"2020","journal-title":"Comp. Biochem. Physiol. D Genom. Proteom."},{"key":"ref_120","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1111\/j.1365-313X.2004.02272.x","article-title":"Identification of novel heat shock factor-dependent genes and biochemical pathways in Arabidopsis thaliana","volume":"41","author":"Busch","year":"2005","journal-title":"Plant J."},{"key":"ref_121","doi-asserted-by":"crossref","first-page":"244","DOI":"10.1016\/j.tplants.2004.03.006","article-title":"Role of plant heat-shock proteins and molecular chaperones in the abiotic stress response","volume":"9","author":"Wang","year":"2004","journal-title":"Trends Plant Sci."},{"key":"ref_122","doi-asserted-by":"crossref","first-page":"185","DOI":"10.1016\/j.plantsci.2011.10.006","article-title":"Hydrogen sulfide donor sodium hydrosulfide-induced heat tolerance in tobacco (Nicotiana tabacum L.) suspension cultured cells and involvement of Ca2+ and calmodulin","volume":"185","author":"Li","year":"2012","journal-title":"Plant Sci."},{"key":"ref_123","doi-asserted-by":"crossref","first-page":"e1961","DOI":"10.7717\/peerj.1961","article-title":"Heat shock factors in tomatoes: Genome-wide identification, phylogenetic analysis and expression profiling under development and heat stress","volume":"4","author":"Yang","year":"2016","journal-title":"Peer J."},{"key":"ref_124","doi-asserted-by":"crossref","first-page":"868","DOI":"10.1038\/s41598-017-01046-2","article-title":"Hydrogen sulfide toxicity inhibits primary root growth through the ROS-NO pathway","volume":"7","author":"Zhang","year":"2017","journal-title":"Sci. Rep."},{"key":"ref_125","doi-asserted-by":"crossref","first-page":"8251","DOI":"10.1038\/srep08251","article-title":"Hydrogen sulfide modulates actin-dependent auxin transport via regulating ABPs results in changing of root development in Arabidopsis","volume":"5","author":"Jia","year":"2015","journal-title":"Sci. Rep."},{"key":"ref_126","doi-asserted-by":"crossref","first-page":"741","DOI":"10.1016\/j.jplph.2012.12.018","article-title":"Hydrogen sulfide donor sodium hydrosulfide-improved heat tolerance in maize and involvement of proline","volume":"170","author":"Li","year":"2013","journal-title":"J. Plant Physiol."},{"key":"ref_127","doi-asserted-by":"crossref","first-page":"1953","DOI":"10.1093\/jxb\/ert055","article-title":"Hydrogen sulfide induces systemic tolerance to salinity and non-ionic osmotic stress in strawberry plants through modification of reactive species biosynthesis and transcriptional regulation of multiple defence pathways","volume":"64","author":"Christou","year":"2013","journal-title":"J. Exp. Bot."},{"key":"ref_128","doi-asserted-by":"crossref","first-page":"e22478","DOI":"10.4161\/psb.22478","article-title":"Cross-talk between sulfur assimilation and ethylene signaling in plants","volume":"8","author":"Iqbal","year":"2013","journal-title":"Plant Signal. Behav."},{"key":"ref_129","doi-asserted-by":"crossref","first-page":"2745","DOI":"10.1016\/S2095-3119(16)61358-8","article-title":"Foliar application of sodium hydrosulfide (NaHS), a hydrogen sulfide (H2S) donor, can protect seedlings against heat stress in wheat (Triticum aestivum L.)","volume":"15","author":"Min","year":"2016","journal-title":"J. Integr. Agric."},{"key":"ref_130","doi-asserted-by":"crossref","first-page":"46","DOI":"10.1016\/j.envexpbot.2014.05.009","article-title":"Systemic mitigation of salt stress by hydrogen peroxide and sodium nitroprusside in strawberry plants via transcriptional regulation of enzymatic and non-enzymatic antioxidants","volume":"107","author":"Christou","year":"2014","journal-title":"Environ. Exp. Bot."},{"key":"ref_131","doi-asserted-by":"crossref","first-page":"1001","DOI":"10.2478\/s11756-014-0396-2","article-title":"Effect of pretreatment with hydrogen sulfide donor sodium hydrosulfide on heat tolerance in relation to antioxidant system in maize (Zea mays L.) seedlings","volume":"69","author":"Li","year":"2014","journal-title":"Biologia"},{"key":"ref_132","doi-asserted-by":"crossref","first-page":"121","DOI":"10.1016\/j.jplph.2014.12.018","article-title":"Hydrogen sulfide acts as a downstream signal molecule in salicylic acid-induced heat tolerance in maize (Zea mays L.) seedlings","volume":"177","author":"Li","year":"2015","journal-title":"J. Plant Physiol."},{"key":"ref_133","doi-asserted-by":"crossref","first-page":"20","DOI":"10.1186\/1999-3110-55-20","article-title":"Involvement of trehalose in hydrogen sulfide donor sodium hydrosulfide-induced the acquisition of heat tolerance in maize (Zea mays L.) seedlings","volume":"55","author":"Li","year":"2014","journal-title":"Bot. Stud."},{"key":"ref_134","doi-asserted-by":"crossref","unstructured":"Banerjee, A., and Roychoudhury, A. (2021). Roles of hydrogen sulfide in regulating temperature stress response in plants. Plant Growth Regulators, Springer.","DOI":"10.1007\/978-3-030-61153-8_10"},{"key":"ref_135","doi-asserted-by":"crossref","first-page":"428","DOI":"10.1007\/s11627-015-9705-x","article-title":"Involvement of sulfhydryl compounds and antioxidant enzymes in H2S-induced heat tolerance in tobacco (Nicotiana tabacum L.) suspension-cultured cells","volume":"51","author":"Li","year":"2015","journal-title":"Vitr. Cell. Dev. Biol. Plant"},{"key":"ref_136","doi-asserted-by":"crossref","first-page":"670","DOI":"10.1590\/S1413-70542006000400012","article-title":"Temperature response of photosynthesis and its interaction with light intensity in sweet orange leaf discs under non-photorespiratory condition","volume":"30","author":"Ribeiro","year":"2006","journal-title":"Ci\u00eancia Agrotecnologia"},{"key":"ref_137","doi-asserted-by":"crossref","first-page":"plx025","DOI":"10.1093\/aobpla\/plx025","article-title":"Plant responses to environmental stresses\u2014from gene to biotechnology","volume":"9","author":"Ahanger","year":"2017","journal-title":"AoB Plants"},{"key":"ref_138","first-page":"332","article-title":"Heat stress and plant development: Role of sulphur metabolites and management strategies","volume":"69","author":"Ihsan","year":"2019","journal-title":"Acta Agric. Scand. Sect. B Soil Plant Sci."},{"key":"ref_139","doi-asserted-by":"crossref","first-page":"plv001","DOI":"10.1093\/aobpla\/plv001","article-title":"Influence of sulfur and cadmium on antioxidants, phytochelatins and growth in Indian mustard","volume":"7","author":"Bashir","year":"2015","journal-title":"AoB Plants"},{"key":"ref_140","doi-asserted-by":"crossref","unstructured":"North, K.A., and Kopriva, S. (2007). Sulfur in resistance to environmental stresses. Sulfur in Plants. An Ecological Perspective, Springer.","DOI":"10.1007\/978-1-4020-5887-5_7"},{"key":"ref_141","doi-asserted-by":"crossref","first-page":"676","DOI":"10.1104\/pp.20.00906","article-title":"Redox modification of the iron-sulfur glutaredoxin GRXS17 activates holdase activity and protects plants from heat stress","volume":"184","author":"Martins","year":"2020","journal-title":"Plant Physiol."},{"key":"ref_142","first-page":"213","article-title":"Heat stress during seed filling interferes with sulfur restriction on grain composition and seed germination in oilseed rape (Brassica napus L.)","volume":"6","author":"Kim","year":"2015","journal-title":"Front. Plant Sci."},{"key":"ref_143","doi-asserted-by":"crossref","first-page":"369","DOI":"10.1080\/01904167.2021.1985138","article-title":"Foliar application of sulfur improved growth, yield and physiological attributes of canola (Brassica napus L.) under heat stress conditions","volume":"45","author":"Waraich","year":"2022","journal-title":"J. Plant Nutr."},{"key":"ref_144","doi-asserted-by":"crossref","unstructured":"Waraich, E.A., Ahmad, M., Soufan, W., Manzoor, M.T., Ahmad, Z., Habib-Ur-Rahman, M., and Sabagh, A.E. (2021). Seed priming with sulfhydral thiourea enhances the performance of Camelina sativa L. under heat stress conditions. Agronomy, 11.","DOI":"10.3390\/agronomy11091875"},{"key":"ref_145","doi-asserted-by":"crossref","unstructured":"Ali, M.M., Waleed Shafique, M., Gull, S., Afzal Naveed, W., Javed, T., Yousef, A.F., and Mauro, R.P. (2021). Alleviation of heat stress in tomato by exogenous application of sulfur. Horticulturae, 7.","DOI":"10.3390\/horticulturae7020021"},{"key":"ref_146","doi-asserted-by":"crossref","unstructured":"Altaf, A., Zhu, X., Zhu, M., Quan, M., Irshad, S., Xu, D., and Zada, A. (2021). Effects of Environmental Stresses (Heat, Salt, Waterlogging) on Grain Yield and Associated Traits of Wheat under Application of Sulfur-Coated Urea. Agronomy, 11.","DOI":"10.3390\/agronomy11112340"},{"key":"ref_147","doi-asserted-by":"crossref","first-page":"171","DOI":"10.1016\/j.pbi.2004.01.015","article-title":"Post-translational modification of therapeutic proteins in plants","volume":"7","author":"Gomord","year":"2004","journal-title":"Curr. Opin. Plant Biol."},{"key":"ref_148","doi-asserted-by":"crossref","first-page":"165","DOI":"10.1093\/jxb\/50.331.165","article-title":"Cis-elements of protein transport to the plant vacuoles","volume":"50","author":"Matsuoka","year":"1999","journal-title":"J. Exp. Bot."},{"key":"ref_149","doi-asserted-by":"crossref","first-page":"161","DOI":"10.1016\/B978-0-12-405210-9.00005-9","article-title":"New insights into the role of the small ubiquitin-like modifier (SUMO) in plants","volume":"300","author":"Park","year":"2013","journal-title":"Int. Rev. Cell Mol. Biol."},{"key":"ref_150","doi-asserted-by":"crossref","first-page":"122","DOI":"10.3389\/fpls.2018.00122","article-title":"Plant abiotic stress proteomics: The major factors determining alterations in cellular proteome","volume":"9","author":"Urban","year":"2018","journal-title":"Front. Plant Sci."},{"key":"ref_151","doi-asserted-by":"crossref","first-page":"6862","DOI":"10.1074\/jbc.M209694200","article-title":"The small ubiqui tin-like modifier (SUMO) protein modification system in Arabidopsis: Accumulation of SUMO1 and-2 conjugates is increased by stress","volume":"278","author":"Kurepa","year":"2003","journal-title":"J. Biol. Chem."},{"key":"ref_152","doi-asserted-by":"crossref","first-page":"119","DOI":"10.1104\/pp.107.102285","article-title":"Genetic analysis of SUMOylation in Arabidopsis: Conjugation of SUMO1 and SUMO2 to nuclear proteins is essential","volume":"145","author":"Saracco","year":"2007","journal-title":"Plant Physiol."},{"key":"ref_153","doi-asserted-by":"crossref","first-page":"735","DOI":"10.1093\/pcp\/pcx032","article-title":"Overexpression of the rice SUMO E3 ligase gene OsSIZ1 in cotton enhances drought and heat tolerance, and substantially improves fiber yields in the field under reduced irrigation and rainfed conditions","volume":"58","author":"Mishra","year":"2017","journal-title":"Plant Cell Physiol."},{"key":"ref_154","doi-asserted-by":"crossref","first-page":"1031","DOI":"10.1111\/tpj.13739","article-title":"Rice SUMO protease Overly Tolerant to Salt 1 targets the transcription factor, Osb ZIP 23 to promote drought tolerance in rice","volume":"92","author":"Srivastava","year":"2017","journal-title":"Plant J."},{"key":"ref_155","doi-asserted-by":"crossref","first-page":"102","DOI":"10.1111\/jipb.12514","article-title":"A novel tomato SUMO E3 ligase, SlSIZ1, confers drought tolerance in transgenic tobacco","volume":"59","author":"Zhang","year":"2017","journal-title":"J. Integr. Plant Biol."},{"key":"ref_156","doi-asserted-by":"crossref","first-page":"113","DOI":"10.1016\/j.plantsci.2019.01.020","article-title":"Overexpression of a maize SUMO conjugating enzyme gene (ZmSCE1e) increases Sumoylation levels and enhances salt and drought tolerance in transgenic tobacco","volume":"281","author":"Wang","year":"2019","journal-title":"Plant Sci."},{"key":"ref_157","doi-asserted-by":"crossref","first-page":"1077","DOI":"10.1105\/tpc.17.00993","article-title":"SUMOylome profiling reveals a diverse array of nuclear targets modified by the SUMO ligase SIZ1 during heat stress","volume":"30","author":"Rytz","year":"2018","journal-title":"Plant Cell"},{"key":"ref_158","doi-asserted-by":"crossref","first-page":"58","DOI":"10.1093\/pcp\/pcx160","article-title":"SUMO E3 ligase SlSIZ1 facilitates heat tolerance in tomato","volume":"59","author":"Zhang","year":"2018","journal-title":"Plant Cell Physiol."},{"key":"ref_159","doi-asserted-by":"crossref","first-page":"1600263","DOI":"10.1002\/bies.201600263","article-title":"Chromatin sumoylation in heat stress: To protect, pause and organise? Sumo stress response on chromatin","volume":"39","author":"Niskanen","year":"2017","journal-title":"BioEssays"},{"key":"ref_160","doi-asserted-by":"crossref","first-page":"1069","DOI":"10.1590\/S1415-47572012000600023","article-title":"MicroRNAs play critical roles during plant development and in response to abiotic stresses","volume":"35","author":"Lima","year":"2012","journal-title":"Gene. Mol. Biol."},{"key":"ref_161","doi-asserted-by":"crossref","first-page":"137","DOI":"10.1016\/j.bbagrm.2011.05.001","article-title":"Role of miRNAs and siRNAs in biotic and abiotic stress responses of plants","volume":"1819","author":"Khraiwesh","year":"2012","journal-title":"Biochim. Biophys. Acta (BBA) Gene Regul. Mech."},{"key":"ref_162","doi-asserted-by":"crossref","first-page":"2051","DOI":"10.1105\/tpc.106.041673","article-title":"Posttranscriptional induction of two Cu\/Zn superoxide dismutase genes in Arabidopsis is mediated by downregulation of miR398 and important for oxidative stress tolerance","volume":"18","author":"Sunkar","year":"2006","journal-title":"Plant Cell"},{"key":"ref_163","doi-asserted-by":"crossref","first-page":"310","DOI":"10.1016\/j.pbi.2007.04.011","article-title":"Complexity of the heat stress response in plants","volume":"10","author":"Kotak","year":"2007","journal-title":"Curr. Opin. Plant Biol."},{"key":"ref_164","doi-asserted-by":"crossref","first-page":"1025","DOI":"10.1093\/jxb\/err337","article-title":"Identification of conserved and novel microRNAs that are responsive to heat stress in Brassica rapa","volume":"63","author":"Yu","year":"2012","journal-title":"J. Exp. Bot."},{"key":"ref_165","doi-asserted-by":"crossref","first-page":"323","DOI":"10.1007\/s10142-014-0421-0","article-title":"Novel and conserved heat-responsive microRNAs in wheat (Triticum aestivum L.)","volume":"15","author":"Kumar","year":"2015","journal-title":"Funct. Integr. Geno."},{"key":"ref_166","doi-asserted-by":"crossref","first-page":"592","DOI":"10.1111\/j.1365-313X.2006.02980.x","article-title":"ABA induction of miR159 controls transcript levels of two MYB factors during Arabidopsis seed germination","volume":"49","author":"Reyes","year":"2007","journal-title":"Plant J."},{"key":"ref_167","doi-asserted-by":"crossref","unstructured":"Wang, Y., Sun, F., Cao, H., Peng, H., Ni, Z., Sun, Q., and Yao, Y. (2012). TamiR159 directed wheat TaGAMYB cleavage and its involvement in anther development and heat response. PLoS ONE, 7.","DOI":"10.1371\/journal.pone.0048445"},{"key":"ref_168","doi-asserted-by":"crossref","first-page":"187","DOI":"10.1007\/s10142-010-0163-6","article-title":"Non-coding small RNAs responsive to abiotic stress in wheat (Triticum aestivum L.)","volume":"10","author":"Yao","year":"2010","journal-title":"Funct. Integr. Geno."},{"key":"ref_169","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1038\/nature09861","article-title":"An siRNA pathway prevents transgenerational retrotransposition in plants subjected to stress","volume":"472","author":"Ito","year":"2011","journal-title":"Nature"},{"key":"ref_170","doi-asserted-by":"crossref","first-page":"1764","DOI":"10.1105\/tpc.114.124883","article-title":"Heat-induced tas1 target1 mediates thermotolerance via heat stress transcription factor A1a\u2013directed pathways in Arabidopsis","volume":"26","author":"Li","year":"2014","journal-title":"Plant Cell"},{"key":"ref_171","doi-asserted-by":"crossref","first-page":"517","DOI":"10.1016\/j.pbi.2012.08.008","article-title":"The role of long non-coding RNA in transcriptional gene silencing","volume":"15","author":"Wierzbicki","year":"2012","journal-title":"Curr. Opin. Plant Biol."},{"key":"ref_172","doi-asserted-by":"crossref","first-page":"297","DOI":"10.1186\/s12864-016-2625-2","article-title":"Temperature expression patterns of genes and their coexpression with LncRNAs revealed by RNA-Seq in non-heading Chinese cabbage","volume":"17","author":"Song","year":"2016","journal-title":"BMC Geno."},{"key":"ref_173","doi-asserted-by":"crossref","first-page":"313","DOI":"10.1007\/s11103-017-0653-1","article-title":"Heat stress differentially modifies ethylene biosynthesis and signaling in pea floral and fruit tissues","volume":"95","author":"Savada","year":"2017","journal-title":"Plant Mol. Biol."},{"key":"ref_174","doi-asserted-by":"crossref","first-page":"271","DOI":"10.1111\/nph.14367","article-title":"Phenotypic and genome-wide association analysis of spike ethylene in diverse wheat genotypes under heat stress","volume":"214","author":"Valluru","year":"2017","journal-title":"New Phytol."},{"key":"ref_175","doi-asserted-by":"crossref","first-page":"323","DOI":"10.5423\/PPJ.RW.08.2015.0150","article-title":"Heat shock proteins: A review of the molecular chaperones for plant immunity","volume":"31","author":"Park","year":"2015","journal-title":"Plant Pathol. J."},{"key":"ref_176","doi-asserted-by":"crossref","first-page":"116","DOI":"10.1016\/j.jphotobiol.2014.01.010","article-title":"Photosynthesis: Response to high temperature stress","volume":"137","author":"Mathur","year":"2014","journal-title":"J. Photochem. Photobiol. B Biol."},{"key":"ref_177","doi-asserted-by":"crossref","first-page":"563","DOI":"10.1007\/s00425-019-03192-5","article-title":"Role of ethylene biosynthesis and signaling in elevated CO2-induced heat stress response in tomato","volume":"250","author":"Pan","year":"2019","journal-title":"Planta"},{"key":"ref_178","doi-asserted-by":"crossref","first-page":"1009","DOI":"10.1007\/BF00016073","article-title":"Comparison of the expression of several stress-responsive genes in potato tubers","volume":"16","author":"Rickey","year":"1991","journal-title":"Plant Mol. Biol."},{"key":"ref_179","doi-asserted-by":"crossref","first-page":"651","DOI":"10.1007\/s00217-008-0974-z","article-title":"Inhibition of wound-induced ethylene does not prevent red discoloration in fresh-cut endive (Cichorium intybus L.)","volume":"228","author":"Salman","year":"2009","journal-title":"Eur. Food Res. Technol."},{"key":"ref_180","doi-asserted-by":"crossref","first-page":"405","DOI":"10.1111\/pbi.12659","article-title":"The heat-shock protein\/chaperone network and multiple stress resistance","volume":"15","author":"Jacob","year":"2017","journal-title":"Plant Biotechnol. J."},{"key":"ref_181","doi-asserted-by":"crossref","first-page":"3661","DOI":"10.1242\/dev.126.16.3661","article-title":"Regulation of differential growth in the apical hook of Arabidopsis","volume":"126","author":"Raz","year":"1999","journal-title":"Development"},{"key":"ref_182","doi-asserted-by":"crossref","first-page":"6123","DOI":"10.1093\/jxb\/eru353","article-title":"Transcriptionally and post-transcriptionally regulated microRNAs in heat stress response in barley","volume":"65","author":"Kruszka","year":"2014","journal-title":"J. Exp. Bot."},{"key":"ref_183","doi-asserted-by":"crossref","first-page":"784","DOI":"10.1038\/s41477-018-0249-z","article-title":"Genome encode analyses reveal the basis of convergent evolution of fleshy fruit ripening","volume":"4","author":"Yu","year":"2018","journal-title":"Nat. Plants"},{"key":"ref_184","doi-asserted-by":"crossref","first-page":"1618","DOI":"10.1111\/nph.16233","article-title":"Genome-wide analysis of coding and non-coding RNA reveals a conserved miR164-NAC regulatory pathway for fruit ripening","volume":"225","author":"Wang","year":"2020","journal-title":"New Phytol."},{"key":"ref_185","doi-asserted-by":"crossref","first-page":"16","DOI":"10.1007\/s11738-015-2038-x","article-title":"Hydrogen sulfide: A versatile regulator of environmental stress in plants","volume":"38","author":"Guo","year":"2016","journal-title":"Acta Physiol. Plant."},{"key":"ref_186","doi-asserted-by":"crossref","first-page":"1415","DOI":"10.1007\/s00709-020-01516-x","article-title":"Interplay between hydrogen sulfide and methylglyoxal initiates thermotolerance in maize seedlings by modulating reactive oxidative species and osmolyte metabolism","volume":"257","author":"Ye","year":"2020","journal-title":"Protoplasma"},{"key":"ref_187","doi-asserted-by":"crossref","first-page":"ra72","DOI":"10.1126\/scisignal.2000464","article-title":"H2S signals through protein S-sulfhydration","volume":"2","author":"Mustafa","year":"2009","journal-title":"Sci. Signal."},{"key":"ref_188","doi-asserted-by":"crossref","first-page":"334","DOI":"10.1104\/pp.15.00009","article-title":"S-sulfhydration: A cysteine posttranslational modification in plant systems","volume":"168","author":"Aroca","year":"2015","journal-title":"Plant Physiol."},{"key":"ref_189","doi-asserted-by":"crossref","first-page":"983","DOI":"10.1093\/pcp\/pcx056","article-title":"Hydrogen sulfide regulates the cytosolic\/nuclear partitioning of glyceraldehyde-3-phosphate dehydrogenase by enhancing its nuclear localization","volume":"58","author":"Aroca","year":"2017","journal-title":"Plant Cell Physiol."},{"key":"ref_190","doi-asserted-by":"crossref","first-page":"2945","DOI":"10.1093\/jxb\/erv146","article-title":"The thioredoxin\/peroxiredoxin\/sulfiredoxin system: Current overview on its redox function in plants and regulation by reactive oxygen and nitrogen species","volume":"66","author":"Sevilla","year":"2015","journal-title":"J. Exp. Bot."},{"key":"ref_191","doi-asserted-by":"crossref","first-page":"3414","DOI":"10.1039\/C5SC04818D","article-title":"Improved tag-switch method reveals that thioredoxin acts as depersulfidase and controls the intracellular levels of protein persulfidation","volume":"7","author":"Wedmann","year":"2016","journal-title":"Chem. Sci."},{"key":"ref_192","doi-asserted-by":"crossref","first-page":"146","DOI":"10.1111\/jipb.13022","article-title":"Hydrogen sulfide, a signaling molecule in plant stress responses","volume":"63","author":"Zhang","year":"2021","journal-title":"J. Integ. Plant Biol."},{"key":"ref_193","doi-asserted-by":"crossref","first-page":"470","DOI":"10.1111\/j.1742-4658.2007.06214.x","article-title":"A cysteine residue near the propionate side chain of heme is the radical site in ascorbate peroxidase","volume":"275","author":"Kitajima","year":"2008","journal-title":"FEBS J."},{"key":"ref_194","doi-asserted-by":"crossref","first-page":"527","DOI":"10.1093\/jxb\/ert396","article-title":"Dual regulation of cytosolic ascorbate peroxidase (APX) by tyrosine nitration and S-nitrosylation","volume":"65","author":"Chaki","year":"2014","journal-title":"J. Exp. Bot."},{"key":"ref_195","doi-asserted-by":"crossref","first-page":"241","DOI":"10.1007\/s11010-015-2383-5","article-title":"Hydrogen sulfide mitigates homocysteine-mediated pathological remodeling by inducing miR-133a in cardiomyocytes","volume":"404","author":"Kesherwani","year":"2015","journal-title":"Mol. Cell. Biochem."},{"key":"ref_196","doi-asserted-by":"crossref","first-page":"1517","DOI":"10.3389\/fpls.2018.01517","article-title":"Ethylene-induced hydrogen sulfide negatively regulates ethylene biosynthesis by persulfidation of ACO in tomato under osmotic stress","volume":"9","author":"Jia","year":"2018","journal-title":"Front. Plant Sci."},{"key":"ref_197","doi-asserted-by":"crossref","first-page":"342","DOI":"10.1016\/j.bbrc.2011.08.101","article-title":"Hydrogen sulphide inhibits cardiomyocyte hypertrophy by up-regulating miR-133a","volume":"413","author":"Liu","year":"2011","journal-title":"Biochem. Biophys. Res. Commun."},{"key":"ref_198","doi-asserted-by":"crossref","first-page":"3192","DOI":"10.1002\/jcp.24006","article-title":"MicroRNA-21 represses human cystathionine gamma-lyase expression by targeting at specificity protein-1 in smooth muscle cells","volume":"227","author":"Yang","year":"2012","journal-title":"J. Cell. Physiol."},{"key":"ref_199","doi-asserted-by":"crossref","first-page":"1866","DOI":"10.1105\/tpc.105.033589","article-title":"Redox homeostasis and antioxidant signaling: A metabolic interface between stress perception and physiological responses","volume":"17","author":"Foyer","year":"2005","journal-title":"Plant Cell"},{"key":"ref_200","doi-asserted-by":"crossref","first-page":"66","DOI":"10.1007\/s00344-008-9075-2","article-title":"Glutathione as an antioxidant and regulatory molecule in plants under abiotic stress conditions","volume":"28","author":"Szalai","year":"2009","journal-title":"J. Plant Growth Regul."},{"key":"ref_201","unstructured":"Renneberg, H., Brunold, C., De Kok, L.J., and Stulen, I. (1990). Sulfur metabolism in plants exposed to atmospheric sulphur. Sulfur Nutrition and Sulfur Assimilation in Higher Plants: Fundamental, Environmental and Agricultural Aspects, Backhuys Publishers."},{"key":"ref_202","first-page":"121","article-title":"Negative vs. positive functional plant responses to air pollution: A study establishing cause\u2013effect relationships of SO2 and H2S","volume":"9","author":"Yang","year":"2009","journal-title":"Dev. Environ. Sci."},{"key":"ref_203","doi-asserted-by":"crossref","first-page":"318","DOI":"10.1071\/FP07283","article-title":"Regulation of sulfate uptake, expression of the sulfate transporters Sultr1; 1 and Sultr1; 2, and APS reductase in Chinese cabbage (Brassica pekinensis) as affected by atmospheric H2S nutrition and sulfate deprivation","volume":"35","author":"Koralewska","year":"2008","journal-title":"Funct. Plant Biol."},{"key":"ref_204","doi-asserted-by":"crossref","first-page":"6911","DOI":"10.1073\/pnas.88.16.6911","article-title":"Isolation of a cDNA for HSF2: Evidence for two heat shock factor genes in humans","volume":"88","author":"Schuetz","year":"1991","journal-title":"Proc. Natl. Acad. Sci. USA"},{"key":"ref_205","doi-asserted-by":"crossref","first-page":"165","DOI":"10.1111\/j.1469-8137.2011.03889.x","article-title":"Cysteine homeostasis plays an essential role in plant immunity","volume":"193","author":"Romero","year":"2012","journal-title":"New Phytol."},{"key":"ref_206","doi-asserted-by":"crossref","first-page":"1028","DOI":"10.4161\/psb.5.8.12296","article-title":"Low abundance does not mean less importance in cysteine metabolism","volume":"5","author":"Gotor","year":"2010","journal-title":"Plant Signal. Behav."},{"key":"ref_207","doi-asserted-by":"crossref","first-page":"1053","DOI":"10.3389\/fpls.2015.01053","article-title":"Links between ethylene and sulfur nutrition\u2014a regulatory interplay or just metabolite association?","volume":"6","author":"Wawrzynska","year":"2015","journal-title":"Front. Plant Sci."},{"key":"ref_208","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/j.plaphy.2016.03.017","article-title":"Involvement of ethylene in gibberellic acid-induced sulfur assimilation, photosynthetic responses, and alleviation of cadmium stress in mustard","volume":"104","author":"Masood","year":"2016","journal-title":"Plant Physiol. Biochem."},{"key":"ref_209","doi-asserted-by":"crossref","first-page":"331","DOI":"10.1111\/ppl.12173","article-title":"Involvement of ethylene in reversal of salt-inhibited photosynthesis by sulfur in mustard","volume":"152","author":"Nazar","year":"2014","journal-title":"Physiol. Plantar."},{"key":"ref_210","doi-asserted-by":"crossref","first-page":"9","DOI":"10.1016\/j.jplph.2014.09.011","article-title":"Selenium and sulfur influence ethylene formation and alleviate cadmium-induced oxidative stress by improving proline and glutathione production in wheat","volume":"173","author":"Khan","year":"2015","journal-title":"J. Plant Physiol."},{"key":"ref_211","doi-asserted-by":"crossref","first-page":"1576","DOI":"10.1002\/jsfa.2895","article-title":"Comparative effects of sulfur and nitrogen fertilization and post-harvest processing parameters on the glucotropaeolin content of Tropaeolum majus L.","volume":"87","author":"Bloem","year":"2007","journal-title":"J. Sci. Food Agric."},{"key":"ref_212","doi-asserted-by":"crossref","first-page":"1408","DOI":"10.1104\/pp.107.113175","article-title":"Complex signaling network in regulation of adenosine 5\u2032-phosphosulfate reductase by salt stress in Arabidopsis roots","volume":"146","author":"Koprivova","year":"2008","journal-title":"Plant Physiol."},{"key":"ref_213","doi-asserted-by":"crossref","first-page":"124427","DOI":"10.1016\/j.chemosphere.2019.124427","article-title":"Atmospheric H2S triggers immune damage by activating the TLR-7\/MyD88\/NF-\u03baB pathway and NLRP3 inflammasome in broiler thymus","volume":"237","author":"Hu","year":"2019","journal-title":"Chemosphere"},{"key":"ref_214","doi-asserted-by":"crossref","unstructured":"Iqbal, N., Umar, S., Khan, N.A., and Corpas, F.J. (2021). Nitric oxide and hydrogen sulfide coordinately reduce glucose sensitivity and decrease oxidative stress via ascorbate-glutathione cycle in heat-stressed wheat (Triticum aestivum L.) plants. Antioxidants, 10.","DOI":"10.3390\/antiox10010108"},{"key":"ref_215","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1016\/j.niox.2018.11.003","article-title":"Recent advancements in the mechanism of nitric oxide signaling associated with hydrogen sulfide and melatonin crosstalk during ethylene-induced fruit ripening in plants","volume":"82","author":"Mukherjee","year":"2019","journal-title":"Nitric Oxide"},{"key":"ref_216","doi-asserted-by":"crossref","first-page":"1754","DOI":"10.1093\/pcp\/pcq134","article-title":"Involvement of ethylene and hydrogen peroxide in induction of alternative respiratory pathway in salt-treated Arabidopsis calluses","volume":"51","author":"Wang","year":"2010","journal-title":"Plant Cell Physiol."},{"key":"ref_217","doi-asserted-by":"crossref","first-page":"922","DOI":"10.1111\/ppl.13225","article-title":"Hydrogen peroxide potentiates defense system in presence of sulfur to protect chloroplast damage and photosynthesis of wheat under drought stress","volume":"172","author":"Sehar","year":"2021","journal-title":"Physiol. Plant."},{"key":"ref_218","doi-asserted-by":"crossref","first-page":"696","DOI":"10.3389\/fpls.2020.00696","article-title":"Hydrogen sulfide alleviates waterlogging-induced damage in peach seedlings via enhancing antioxidative system and inhibiting ethylene synthesis","volume":"11","author":"Xiao","year":"2020","journal-title":"Front. Plant Sci."},{"key":"ref_219","doi-asserted-by":"crossref","first-page":"5","DOI":"10.1007\/s00344-017-9704-8","article-title":"Exogenous hydrogen sulfide ameliorates seed germination and seedling growth of cauliflower under lead stress and its antioxidant role","volume":"37","author":"Chen","year":"2018","journal-title":"J. Plant Growth Regul."}],"container-title":["Biomolecules"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.mdpi.com\/2218-273X\/12\/5\/678\/pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2025,10,10]],"date-time":"2025-10-10T23:07:50Z","timestamp":1760137670000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.mdpi.com\/2218-273X\/12\/5\/678"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2022,5,8]]},"references-count":219,"journal-issue":{"issue":"5","published-online":{"date-parts":[[2022,5]]}},"alternative-id":["biom12050678"],"URL":"https:\/\/doi.org\/10.3390\/biom12050678","relation":{},"ISSN":["2218-273X"],"issn-type":[{"value":"2218-273X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2022,5,8]]}}}