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Ameliorative effects of strigolactone on tolerance to lead stress on lettuce (Lactuca sativa L.) plants
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Bioaccumulation of lead (Pb) and its effects in plants: A review
Collin, S., Baskar, A., Geevarghese, D. M., Ali, M. N. V. S., Bahubali, P., Choudhary, R., Lvov, V., Tovar, G. I., Senatov, F., Koppala, S., et al. (2022) · Journal of Hazardous Materials Letters · doi:10.1016/j.hazl.2022.100064 · Cited by 362
Waters, M. T., Brewer, P. B., Bussell, J. D., Smith, S. M., & Beveridge, C. A. (2012) · Plant Physiology · doi:10.1104/pp.112.196253 · Cited by 232
Research works printed but not linked: 175
- Ahemad, M. Remediation of metalliferous soils through the heavy metal resistant plant growth promoting bacteria: Paradigms and prospects. Arab. J. Chem. 12, 1365–1377 (2019). · DOI · Paper page
- Sardar, K. et al. Heavy metals contamination and what are the impacts on living organisms. Greener J. Environ. Manag. Public Saf. 2, 172–179 (2013). · DOI · Paper page
- Liang, C., Xiao, H., Hu, Z., Zhang, X. & Hu, J. Uptake, transportation, and accumulation of C60 fullerene and heavy metal ions (Cd, Cu, and Pb) in rice plants grown in an agricultural soil. Environ. Pollut. 235, 330–338 (2018). · DOI
- Ikkonen, E. & Kaznina, N. Physiological responses of lettuce (Lactuca sativa L.) to soil contamination with Pb. Horticulturae 8, 951 (2022). · DOI
- Kohli, S. K. et al. Current scenario of Pb toxicity in plants: Unraveling plethora of physiological responses. Rev. Environ. Contam. Toxicol. 249, 153–197 (2019).
- Zulfiqar, U. et al. Lead toxicity in plants: Impacts and remediation. J. Environ. Manag. 250, 109557 (2019). · DOI · Paper page
- Kumar, A. & Prasad, M. N. V. Plant-lead interactions: Transport, toxicity, tolerance, and detoxification mechanisms. Ecotoxicol. Environ. Saf. 166, 401–418 (2018). · DOI · Paper page
- Oliveira, D. G. et al. Lonchocarpus cultratus, a Brazilian savanna tree, endures high soil Pb levels. Environ. Sci. Pollut. Res. 28, 50931–50940 (2021). · doi:10.1007/s11356-021-15856-5
- Faizan, M., Cheng, S. H., Tonny, S. H. & Robab, M. I. Specific roles of strigolactones in plant physiology and remediation of heavy metals from contaminated soil. Plant Physiol. Biochem. 192, 186–195 (2022). · DOI
- Mathur, P., Tripathi, D. K., Baluška, F. & Mukherjee, S. Auxin-mediated molecular mechanisms of heavy metal and metalloid stress regulation in plants. Environ. Exp. Bot. 196, 104796 (2022). · DOI
- Bano, A., Singh, K., Singh, S. P. & Sharma, P. Abscisic Acid: Metabolism, signaling, and crosstalk with other phytohormones under heavy metal stress. Stresses 3, 665–686 (2023). · DOI
- Osakabe, Y., Yamaguchi-Shinozaki, K., Shinozaki, K. & Tran, L. S. P. ABA control of plant macroelement membrane transport systems in response to water deficit and high salinity. New Phytol. 202, 35–49 (2014). · DOI · Paper page
- Kour, J. et al. Brassinosteroid signaling, crosstalk and physiological functions in plants under heavy metal stress. Front. Plant Sci. 12, 608061 (2021). · DOI · Paper page
- Talaat, N. B. & Shawky, B. T. Dual application of 24-epibrassinolide and spermine confers drought stress tolerance in maize (Zea mays L.) by modulating polyamine and protein metabolism. J. Plant Growth Regul. 35, 518–533 (2016). · DOI
- Colebrook, E. H., Thomas, S. G., Phillips, A. L. & Hedden, P. The role of gibberellin signalling in plant responses to abiotic stress. J. Exp. Biol. 217, 67–75 (2014). · DOI · Paper page
- Falkowska, M. et al. The effect of gibberellic acid (GA3) on growth, metal biosorption and metabolism of the green algae Chlorella vulgaris (Chlorophyceae) Beijerinck exposed to cadmium and lead stress. Pol. J. Environ. Stud. 20, 53–59 (2011).
- Chen, X. et al. Transcriptomic and metabolomic analyses reveal that exogenous strigolactones alleviate the response of melon root to cadmium stress. Hortic. Plant J. 8, 637–649 (2022). · DOI
- Ling, F. et al. Effects of strigolactone on photosynthetic and physiological characteristics in salt-stressed rice seedlings. Sci. Rep. 10, 6183 (2020). · DOI · Paper page
- Zulfiqar, H. et al. Strigolactone (GR24) induced salinity tolerance in sunflower (Helianthus annuus L.) by ameliorating morpho-physiological and biochemical attributes under in vitro conditions. J. Plant Growth Regul. 40, 2079–2091 (2021). · DOI
- Zhou, X. et al. Physiological mechanism of strigolactone enhancing tolerance to low light stress in cucumber seedlings. BMC Plant Biol. 22, 30 (2022). · doi:10.1186/s12870-021-03414-7
- Mostofa, M. G., Li, W., Nguyen, K. H., Fujita, M. & Tran, L. S. P. Strigolactones in plant adaptation to abiotic stresses: An emerging avenue of plant research. Plant Cell Environ. 41, 2227–2243 (2018). · DOI · Paper page
- van Zeijl, A. et al. The strigolactone biosynthesis gene DWARF27 is co-opted in rhizobium symbiosis. BMC Plant Biol. 15, 260 (2015). · DOI
- Zhao, B. et al. TaD27-B gene controls the tiller number in hexaploid wheat. Plant Biotechnol. J. 18, 513–525 (2020). · DOI
- Alvi, A. F., Sehar, Z., Fatma, M., Masood, A. & Khan, N. A. Strigolactone: An emerging growth regulator for developing resilience in plants. Plants 11, 2604 (2022). · DOI
- Banerjee, A. & Roychoudhury, A. Strigolactones: multi-level regulation of biosynthesis and diverse responses in plant abiotic stresses. Acta Physiol. Plant. 40, 86 (2018). · DOI
- Wani, K. I. et al. Mechanistic insights into strigolactone biosynthesis, signaling, and regulation during plant growth and development. J. Plant Growth Regul. 40, 1836–1852 (2021). · DOI
- Wani, K. I. et al. Exogenous strigolactone (GR24) positively regulates growth, photosynthesis, and improves glandular trichome attributes for enhanced artemisinin production in Artemisia annua. J. Plant Growth Regul. 42, 4606–4615 (2023). · DOI
- Sun, J. et al. Detection for lead pollution level of lettuce leaves based on deep belief network combined with hyperspectral image technology. J. Food Saf. 41, e12866 (2021). · DOI
- Zhou, X. et al. Development of deep learning method for lead content prediction of lettuce leaf using hyperspectral images. Int. J. Remote Sens. 41, 2263–2276 (2020). · DOI
- Li, J. et al. Lead and copper-induced hormetic effect and toxicity mechanisms in lettuce (Lactuca sativa L.) grown in a contaminated soil. Sci. Total Environ. 741, 140440 (2020). · DOI
- Li, N. et al. Concentration and transportation of heavy metals in vegetables and risk assessment of human exposure to bioaccessible heavy metals in soil near a waste-incinerator site south China. Sci. Total Environ. 521, 144–151 (2015). · DOI · Paper page
- Arshad, A. et al. In Phytohormones and Stress Responsive Secondary Metabolites (Elsevier, 2023).
- Liu, H. et al. Strigolactone is involved in nitric oxide-enhanced the salt resistance in tomato seedlings. J. Plant Res. 135, 337–350 (2022). · DOI
- Sedaghat, M. et al. The potential of the synthetic strigolactone analogue GR24 for the maintenance of photosynthesis and yield in winter wheat under drought: investigations on the mechanisms of action and delivery modes. Plants 10, 1223 (2021). · doi:10.3390/plants10061223
- Sharifi, P. & Bidabadi, S. S. Strigolactone could enhances gas-exchange through augmented antioxidant defense system in Salvia nemorosa L. plants subjected to saline conditions stress. Ind. Crops Prod. 151, 112460 (2020). · doi:10.1016/j.indcrop.2020.112460
- Ajorlo, M., Abdullah, R. B. & Ebrahimian, M. Cattle grazing impacts on shoot and root characteristics of Urochloa decumbens (Stapf) R. Webster and Axonopus compressus (Sw.) P. Beauv. in tropical pastures of Malaysia. J. Rangeland Sci. 15, 1–11 (2025).
- Smart, R. E. & Bingham, G. E. Rapid estimates of relative water content. Plant Physiol. 53, 258–260 (1974). · DOI · Paper page
- Ekinci, M., Ors, S., Sahin, U., Yildirim, E. & Dursun, A. Responses to the irrigation water amount of spinach supplemented with organic amendment in greenhouse conditions. Commun. Soil Sci. Plant Anal. 46, 327–342 (2015). · doi:10.1080/00103624.2014.980827
- Lutts, S., Kinet, J. & Bouharmont, J. NaCl-induced senescence in leaves of rice (Oryza sativa L.) cultivars differing in salinity resistance. Ann. Bot. 78, 389–398 (1996). · DOI · Paper page
- Yildirim, E. et al. Exogenous dopamine mitigates the effects of salinity stress in tomato seedlings by alleviating the oxidative stress and regulating phytohormones. Acta Physiol. Plant. 46, 59 (2024). · doi:10.1007/s11738-024-03656-6
- Velikova, V., Yordanov, I. & Edreva, A. Oxidative stress and some antioxidant systems in acid rain-treated bean plants: Protective role of exogenous polyamines. Plant Sci. 151, 59–66 (2000). · DOI · Paper page
- Odjegba, V. J. & Badejo, J. O. Crude oil induced oxidative stress in Capsicum annum L.. Nat. Sci. 11, 46–50 (2013).
- Sun, X., Xie, L. & Han, L. Effects of exogenous spermidine and spermine on antioxidant metabolism associated with cold-induced leaf senescence in Zoysiagrass (Zoysia japonica Steud.). Hortic. Environ. Biotechnol. 60, 295–302 (2019). · doi:10.1007/s13580-018-0089-9
- Bates, L. S., Waldren, R. & Teare, I. Rapid determination of free proline for water-stress studies. Plant Soil 39, 205–207 (1973). · DOI · Paper page
- Liu, X. & Huang, B. Heat stress injury in relation to membrane lipid peroxidation in creeping bentgrass. Crop Sci. 40, 503–510 (2000). · DOI · Paper page
- Ting, S. Fruit juice assay, rapid colormetric methods for simultaneous determination of total reducing sugars and fructose in citrus juices. J. Agric. Food Chem. 4, 263–266 (1956). · DOI
- Angelini, R. & Federico, R. Histochemical evidence of polyamine oxidation and generation of hydrogen peroxide in the cell wall. J. Plant Physiol. 135, 212–217 (1989). · DOI · Paper page
- Balotf, S., Kavoosi, G. & Kholdebarin, B. Nitrate reductase, nitrite reductase, glutamine synthetase, and glutamate synthase expression and activity in response to different nitrogen sources in nitrogen-starved wheat seedlings. Biotechnol. Appl. Biochem. 63, 220–229 (2016). · doi:10.1002/bab.1362
- Angelini, R., Manes, F. & Federico, R. Spatial and functional correlation between diamine-oxidase and peroxidase activities and their dependence upon de-etiolation and wounding in chick-pea stems. Planta 182, 89–96 (1990). · DOI · Paper page
- Yordanova, R. Y., Christov, K. N. & Popova, L. P. Antioxidative enzymes in barley plants subjected to soil flooding. Environ. Exp. Bot. 51, 93–101 (2004). · DOI · Paper page
- Bremner, J. M. Nitrogen-total. Methods Soil Anal. Part 3 Chem. Methods 5, 1085–1121 (1996).
- Mertens, D. Official Methods of Analysis of AOAC INTERNATIONAL (ed George W. Latimer, Jr.) 0 (Oxford University Press, 2023).
- Mertens, P. et al. Grundzüge der Wirtschaftsinformatik (Springer, 2005).
- Abu-Shahba, M. S., Mansour, M. M., Mohamed, H. I. & Sofy, M. R. Effect of biosorptive removal of cadmium ions from hydroponic solution containing indigenous garlic peel and mercerized garlic peel on lettuce productivity. Sci. Hortic. 293, 110727 (2022). · DOI · Paper page
- Xiong, T., Zhang, S., Kang, Z., Zhang, T. & Li, S. Dose-dependent physiological and transcriptomic responses of lettuce (Lactuca sativa L.) to copper oxide nanoparticles—Insights into the phytotoxicity mechanisms. Int. J. Mol. Sci. 22, 3688 (2021). · DOI
- Livak, K. J. & Schmittgen, T. D. Analysis of relative gene expression data using real-time quantitative PCR and the 2−ΔΔCT method. Methods 25, 402–408 (2001). · DOI · Paper page
- Rashid, A. et al. Heavy metal contamination in agricultural soil: environmental pollutants affecting crop health. Agronomy 13, 1521 (2023). · DOI · Paper page
- Alengebawy, A., Abdelkhalek, S. T., Qureshi, S. R. & Wang, M.-Q. Heavy metals and pesticides toxicity in agricultural soil and plants: Ecological risks and human health implications. Toxics 9, 42 (2021). · DOI · Paper page
- Chen, F. et al. Mitigation of lead toxicity in Vigna radiata genotypes by silver nanoparticles. Environ. Pollut. 308, 119606 (2022). · doi:10.1016/j.envpol.2022.119606
- Altaf, M. A. et al. Melatonin enhanced the heavy metal-stress tolerance of pepper by mitigating the oxidative damage and reducing the heavy metal accumulation. J. Hazard. Mater. 454, 131468 (2023). · doi:10.1016/j.jhazmat.2023.131468
- Pandey, A., Sharma, M. & Pandey, G. K. Emerging roles of strigolactones in plant responses to stress and development. Front. Plant Sci. 7, 434 (2016).
- Aslam, M. et al. Lead toxicity in cereals: Mechanistic insight into toxicity, mode of action, and management. Front. Plant Sci. 11, 587785 (2021). · DOI · Paper page
- Li, S. et al. Stabilization of Pb (II) accumulated in biomass through phosphate-pretreated pyrolysis at low temperatures. J. Hazard. Mater. 324, 464–471 (2017). · DOI
- Lin, L., Dolker, T. & Lingling, W. Toxicity of single and combined Pb and Cd stress on antioxidant enzymes and subcellular structure of lettuce. Asian J. Ecotoxicol. 2, 219–230 (2022).
- Malik, B. et al. Lead and aluminium-induced oxidative stress and alteration in the activities of antioxidant enzymes in chicory plants. Sci. Hortic. 278, 109847 (2021). · DOI
- Wani, K. I., Naeem, M., Khan, M. M. A. & Aftab, T. Insights into strigolactone (GR24) mediated regulation of cadmium-induced changes and ROS metabolism in Artemisia annua. J. Hazard. Mater. 448, 130899 (2023). · DOI
- Raja, V. et al. Melatonin and strigolactone mitigate chromium toxicity through modulation of ascorbate-glutathione pathway and gene expression in tomato. Plant Physiol. Biochem. 201, 107872 (2023). · DOI
- Min, Z. et al. Alleviation of drought stress in grapevine by foliar-applied strigolactones. Plant Physiol. Biochem. 135, 99–110 (2019). · DOI · Paper page
- Chi, C. et al. Strigolactones positively regulate abscisic acid-dependent heat and cold tolerance in tomato. Hortic. Res. 8, 237, https://doi.org/10.1038/s41438-021-00668-y (2021). · DOI
- Mi, X. et al. Strigolactone enhances alkaline tolerance in soybean seeds germination by altering expression profiles of ABA biosynthetic and signaling genes. J. Plant Biol. 66, 373–381 (2023). · doi:10.1007/s12374-022-09357-2
- Zhang, R. et al. SLs signal transduction gene CsMAX2 of cucumber positively regulated to salt, drought and ABA stress in Arabidopsis thaliana L.. Gene 864, 147282 (2023). · DOI
- Zhang, Y., Liu, L., Chen, X. & Li, J. Effects of low-temperature stress during the anther differentiation period on winter wheat photosynthetic performance and spike-setting characteristics. Plants 11, 389 (2022). · DOI
- Ni, M., Lin, W., Wei, Z., Hong-fang, L. & Jun, L. Exogenous strigolactones promote lateral root growth by reducing the endogenous auxin level in rapeseed. J. Integr. Agric. 19(465), 482 (2020).
- Andreo-Jimenez, B., Ruyter-Spira, C., Bouwmeester, H. J. & Lopez-Raez, J. A. Ecological relevance of strigolactones in nutrient uptake and other abiotic stresses, and in plant-microbe interactions below-ground. Plant Soil 394, 1–19 (2015). · DOI
- Shtaya, M. J., Yasin, A., Fatoom, J. & Jebreen, M. The effect of salinity on leaf relative water content and chlorophyll content of three wheat (Triticum aestivum L.) landraces from Palestine. Hebron Univ. Res. J. Natur. Sci. 8, 52–65 (2019).
- Bouziani, E.-H., Benouis, S. & Azzouz, F. Effect of pb stress on relative water content, photosynthetic pigments, pb uptake and nutrients (ca, na and k) balance in broad bean (Vicia faba L.) plant. Plant Arch. 23, 36–43 (2023). · doi:10.51470/plantarchives.2023.v23.no1.005
- Shahzad, K. et al. Minimization of heavy metal toxicity in radish (Raphanus sativus) by strigolactone and biochar. Sci. Rep. 14, 13616 (2024). · doi:10.1038/s41598-024-64596-2
- Cunha, A. R. D. et al. Negative effects on photosynthesis and chloroplast pigments exposed to lead and aluminium: A meta-analysis. Cerne 26, 232–237 (2020). · DOI
- Silva, S., Pinto, G. & Santos, C. Low doses of Pb affected Lactuca sativa photosynthetic performance. Photosynthetica 55, 50–57 (2017). · doi:10.1007/s11099-016-0220-z
- Mallhi, Z. I. et al. Citric acid enhances plant growth, photosynthesis, and phytoextraction of lead by alleviating the oxidative stress in castor beans. Plants 8, 525 (2019). · DOI
- Faisal, M. et al. Strigolactone-mediated mitigation of negative effects of salinity stress in Solanum lycopersicum through reducing the oxidative damage. Sustainability 15, 5805 (2023). · DOI
- Ekinci, M., Yildirim, E. & Turan, M. Ameliorating effects of hydrogen sulfide on growth, physiological and biochemical characteristics of eggplant seedlings under salt stress. S. Afr. J. Bot. 143, 79–89 (2021). · doi:10.1016/j.sajb.2021.07.034
- Ihtisham, M. et al. Primary plant nutrients modulate the reactive oxygen species metabolism and mitigate the impact of cold stress in overseeded perennial ryegrass. Front. Plant Sci. 14, 1149832 (2023). · doi:10.3389/fpls.2023.1149832
- Sharma, J. et al. Stress-mitigating behavior of glycine betaine to enhance growth performance by suppressing the oxidative stress in Pb-stressed barley genotypes. Environ. Sci. Pollut. Res. 31, 7498–7513 (2024). · doi:10.1007/s11356-023-31731-x
- Bharwana, S. et al. Alleviation of lead toxicity by silicon is related to elevated photosynthesis, antioxidant enzymes suppressed lead uptake and oxidative stress in cotton. J. Bioremed. Biodegrad. 4, 10–4172 (2013).
- Seifikalhor, M. et al. Calcium signaling and salt tolerance are diversely entwined in plants. Plant Signal. Behav. 14, 1665455 (2019). · DOI · Paper page
- Wang, T.-Z., Zhang, J.-L., Tian, Q.-Y., Zhao, M.-G. & Zhang, W.-H. A Medicago truncatula EF-Hand family gene, MtCaMP1, is involved in drought and salt stress tolerance. PLoS ONE 8, e58952 (2013). · doi:10.1371/journal.pone.0058952
- Iftikhar, I. et al. Resilient mechanism of strigolactone (GR24) in regulating morphological and biochemical status of maize under salt stress. Biocatal. Agric. Biotechnol. 60, 103340 (2024). · doi:10.1016/j.bcab.2024.103340
- Anwar, A., She, M., Wang, K., Riaz, B. & Ye, X. Biological roles of ornithine aminotransferase (OAT) in plant stress tolerance: present progress and future perspectives. Int. J. Mol. Sci. 19, 3681 (2018). · doi:10.3390/ijms19113681
- Kaur, H., Manna, M., Thakur, T., Gautam, V. & Salvi, P. Imperative role of sugar signaling and transport during drought stress responses in plants. Physiol. Plant. 171, 833–848 (2021). · DOI · Paper page
- Gou, C. et al. Integrative application of silicon and/or proline improves Sweet corn (Zea mays L. saccharata) production and antioxidant defense system under salt stress condition. Sci. Rep. 13, 18315 (2023). · DOI
- Riyazuddin, R. et al. A comprehensive review on the heavy metal toxicity and sequestration in plants. Biomolecules 12, 43 (2021). · DOI · Paper page
- Qadir, M. et al. Phytohormones producing Acinetobacter bouvetii P1 mitigates chromate stress in sunflower by provoking host antioxidant response. Antioxidants 10, 1868 (2021). · doi:10.3390/antiox10121868
- Shafi, A., Zahoor, I. & Mushtaq, U. of Tolerance and Adaptation Under Salinity Stress. Salt Stress, Microbes, and Plant Interactions: Mechanisms and Molecular Approaches: Volume 2, 269 (2019). · doi:10.1007/978-981-13-8805-7_13
- Fichman, Y. et al. Evolution of proline biosynthesis: enzymology, bioinformatics, genetics, and transcriptional regulation. Biol. Rev. 90, 1065–1099 (2015). · DOI · Paper page
- Tariq, A. et al. Strigolactones can be a potential tool to fight environmental stresses in arid lands. Environ. Res. 229, 115966 (2023). · DOI
- Sachdev, S., Ansari, S. A., Ansari, M. I., Fujita, M. & Hasanuzzaman, M. Abiotic stress and reactive oxygen species: Generation, signaling, and defense mechanisms. Antioxidants 10, 277 (2021). · DOI · Paper page
- Elbouzidi, A. et al. Elicitor-driven enhancement of phenolic compounds in geranium callus cultures: Phytochemical profiling via LC-MS/MS and biological activities. Front. Chem. 13, 1537877 (2025). · DOI
- Li, S. Novel insight into functions of ascorbate peroxidase in higher plants: More than a simple antioxidant enzyme. Redox Biol. 64, 102789 (2023). · doi:10.1016/j.redox.2023.102789
- Khan, M. et al. Lead (Pb)-induced oxidative stress alters the morphological and physio-biochemical properties of rice (Oryza sativa L.). Agronomy 11, 409 (2021). · doi:10.3390/agronomy11030409
- Fatemi, H., Esmaiel Pour, B. & Rizwan, M. Foliar application of silicon nanoparticles affected the growth, vitamin C, flavonoid, and antioxidant enzyme activities of coriander (Coriandrum sativum L.) plants grown in lead (Pb)-spiked soil. Environ. Sci. Pollut. Res. 28, 1417–1425 (2021). · DOI · Paper page
- Hasanuzzaman, M. et al. Regulation of ascorbate-glutathione pathway in mitigating oxidative damage in plants under abiotic stress. Antioxidants 8, 384 (2019). · DOI · Paper page
- Madhu, et al. Exploration of glutathione reductase for abiotic stress response in bread wheat (Triticum aestivum L.). Plant Cell Rep. 41, 639–654 (2022). · DOI
- Potęga, A. Glutathione-mediated conjugation of anticancer drugs: an overview of reaction mechanisms and biological significance for drug detoxification and bioactivation. Molecules 27, 5252 (2022). · DOI
- Ahanger, M. A., Aziz, U., Alsahli, A. A., Alyemeni, M. N. & Ahmad, P. Combined kinetin and spermidine treatments ameliorate growth and photosynthetic inhibition in Vigna angularis by up-regulating antioxidant and nitrogen metabolism under cadmium stress. Biomolecules 10, 147 (2020). · DOI
- Ma, N. et al. Strigolactones improve plant growth, photosynthesis, and alleviate oxidative stress under salinity in rapeseed (Brassica napus L.) by regulating gene expression. Front. Plant Sci. 8, 1671 (2017). · DOI · Paper page
- Wang, W.-N. et al. Physiological and transcriptomic analysis of Cabernet Sauvginon (Vitis vinifera L.) reveals the alleviating effect of exogenous strigolactones on the response of grapevine to drought stress. Plant Physiol. Biochem. 167, 400–409 (2021). · DOI
- Mostofa, M. G. et al. Strigolactones modulate cellular antioxidant defense mechanisms to mitigate arsenate toxicity in rice shoots. Antioxidants 10, 1815 (2021). · DOI
- Feng, R. et al. Identification, characterization, and stress responsiveness of glucose-6-phosphate dehydrogenase genes in highland barley. Plants 9, 1800 (2020). · doi:10.3390/plants9121800
- Queiroz, R. B. et al. Effect of exogenous tryptophan on primary metabolism and oxidative stress and their relationship with seedling germination and vigor of Glycine max L.. Agronomy 13, 1609 (2023). · DOI
- Bagnato, L. et al. Arabidopsis thaliana sucrose phosphate synthase A2 affects carbon partitioning and drought response. Biology 12, 685 (2023). · DOI
- Scharte, J. et al. Metabolic priming in G6PDH isoenzyme-replaced tobacco lines improves stress tolerance and seed yields via altering assimilate partitioning. Plant J. 116, 1696–1716 (2023). · DOI
- Jin, J. et al. Glucose-6-phosphate dehydrogenase is involved in the tolerance of soybean seedlings to low nitrogen stress. Agronomy 11, 637 (2021). · DOI
- de Freitas-Silva, L. et al. Glyphosate-induced oxidative stress in Arabidopsis thaliana affecting peroxisomal metabolism and triggers activity in the oxidative phase of the pentose phosphate pathway (OxPPP) involved in NADPH generation. J. Plant Physiol. 218, 196–205 (2017). · doi:10.1016/j.jplph.2017.08.007
- Reyes, J. S. et al. Competitive oxidation of key pentose phosphate pathway enzymes modulates the fate of intermediates and NAPDH production. Free Radic. Biol. Med. 222, 505–518 (2024). · DOI
- Huang, J. et al. Glucose-6-phosphate dehydrogenase and abscisic acid mediate programmed cell death induced by aluminum toxicity in soybean root tips. J. Hazard. Mater. 425, 127964 (2022). · doi:10.1016/j.jhazmat.2021.127964
- Santiago, J. P. et al. Contrasting anther glucose-6-phosphate dehydrogenase activities between two bean varieties suggest an important role in reproductive heat tolerance. Plant Cell Environ. 44, 2185–2199 (2021). · DOI
- Song, X., Yin, X., Zhu, Y., Su, Q. & Bao, Y. Evolution of duplicated glutathione metabolic pathway in Gossypium hirsutum and Its Response to UV-B Stress. Ecol. Evol. 14, e70537 (2024). · DOI
- Wang, X. et al. Nitric oxide and hydrogen peroxide increase glucose-6-phosphate dehydrogenase activities and expression upon drought stress in soybean roots. Plant Cell Rep. 39, 63–73 (2020). · DOI
- Wang, X. et al. Persulfidation maintains cytosolic G6PDs activity through changing tetrameric structure and competing cysteine sulfur oxidation under salt stress in Arabidopsis and tomato. New Phytol. 240, 626–643 (2023). · doi:10.1111/nph.19188
- Tian, Y. et al. Glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase genes of winter wheat enhance the cold tolerance of transgenic Arabidopsis. Plant Physiol. Biochem. 161, 86–97 (2021). · doi:10.1016/j.plaphy.2021.02.005
- Landi, S., Capasso, G. & Esposito, S. Different G6PDH isoforms show specific roles in acclimation to cold stress at various growth stages of barley (Hordeum vulgare) and Arabidopsis thaliana. Plant Physiol. Biochem. 169, 190–202 (2021). · DOI
- Berger, A. et al. Plant nitrate reductases regulate nitric oxide production and nitrogen-fixing metabolism during the Medicago truncatula–Sinorhizobium meliloti symbiosis. Front. Plant Sci. 11, 1313 (2020). · doi:10.3389/fpls.2020.01313
- Zhang, X., Franzisky, B. L., Eigner, L., Geilfus, C. M. & Zörb, C. Antagonism of chloride and nitrate inhibits nitrate reductase activity in chloride-stressed maize. Plant Growth Regul. 93, 279–289 (2021). · doi:10.1007/s10725-020-00685-2
- Ashraf, M. A. et al. Effect of exogenous taurine on growth, oxidative defense, and nickel (Ni) uptake in canola (Brassica napus L.) under Ni stress. Physiol. Mol. Biol. Plants 29, 1135–1152 (2023). · DOI
- Oláh, D., Feigl, G., Molnár, Á., Ördög, A. & Kolbert, Z. Strigolactones interact with nitric oxide in regulating root system architecture of Arabidopsis thaliana. Front. Plant Sci. 11, 1019 (2020). · DOI
- Lamhamdi, M. et al. Effect of lead stress on mineral content and growth of wheat (Triticum aestivum) and spinach (Spinacia oleracea) seedlings. Saudi J. Biol. Sci. 20, 29–36 (2013). · DOI · Paper page
- Ke, D. et al. Carotenoid-derived bioactive metabolites shape plant root architecture to adapt to the rhizospheric environments. Front. Plant Sci. 13, 986414 (2022). · DOI
- Bhoi, A., Yadu, B., Chandra, J. & Keshavkant, S. Contribution of strigolactone in plant physiology, hormonal interaction and abiotic stresses. Planta 254, 28 (2021). · DOI
- Tai, Z. et al. Exogenous GR24 alleviates cadmium toxicity by reducing cadmium uptake in switchgrass (Panicum virgatum) seedlings. Int. J. Environ. Res. Public Health 14, 852 (2017). · DOI
- Shi, W.-G. et al. Abscisic acid enhances lead translocation from the roots to the leaves and alleviates its toxicity in Populus× canescens. J. Hazard. Mater. 362, 275–285 (2019). · DOI
- Zhang, Y. et al. The tomato MAX1 homolog, SlMAX1, is involved in the biosynthesis of tomato strigolactones from carlactone. New Phytol. 219, 297–309 (2018). · DOI
- Bhati, K. K. et al. Silencing of ABCC13 transporter in wheat reveals its involvement in grain development, phytic acid accumulation and lateral root formation. J. Exp. Bot. 67, 4379–4389 (2016). · DOI
- Brunetti, P. et al. Cadmium-inducible expression of the ABC-type transporter AtABCC3 increases phytochelatin-mediated cadmium tolerance in Arabidopsis. J. Exp. Bot. 66, 3815–3829 (2015). · DOI · Paper page
- Basu, U. et al. ABC transporter-mediated transport of glutathione conjugates enhances seed yield and quality in chickpea. Plant Physiol. 180, 253–275 (2019). · DOI
- Song, W.-Y. et al. In Plant ABC Transporters (Springer, 2014).
- Korek, M. & Marzec, M. Strigolactones and abscisic acid interactions affect plant development and response to abiotic stresses. BMC Plant Biol. 23, 314 (2023). · DOI
- Wang, R.-K., Wang, C.-E., Fei, Y.-Y., Gai, J.-Y. & Zhao, T.-J. Genome-wide identification and transcription analysis of soybean carotenoid oxygenase genes during abiotic stress treatments. Mol. Biol. Rep. 40, 4737–4745 (2013). · DOI
- Cheng, X., Ruyter-Spira, C. & Bouwmeester, H. The interaction between strigolactones and other plant hormones in the regulation of plant development. Front. Plant Sci. 4, 199 (2013). · DOI · Paper page
- Ding, A., Bao, F., Cheng, W., Cheng, T. & Zhang, Q. Phylogeny of PmCCD gene family and expression analysis of flower coloration and stress response in Prunus mume. Int. J. Mol. Sci. 24, 13950 (2023). · DOI
- Zhang, S. et al. Genome-wide identification, characterization and expression profiles of the CCD gene family in Gossypium species. 3 Biotech 11, 249 (2021). · DOI
- Zhao, J. et al. Genome-wide identification and expression analysis of the carotenoid cleavage oxygenase gene family in five rosaceae species. Plant Mol. Biol. Rep. 39, 739–751 (2021). · DOI
- Kapoor, R. T., Alam, P., Chen, Y. & Ahmad, P. Strigolactones in plants: From development to abiotic stress management. J. Plant Growth Regul. 43, 903–919 (2024). · doi:10.1007/s00344-023-11148-z
- Du, H. et al. Integrative regulation of drought escape through ABA-dependent and-independent pathways in rice. Mol. Plant 11, 584–597 (2018). · DOI · Paper page
- Marzec, M. et al. Barley strigolactone signalling mutant hvd14. D reveals the role of strigolactones in abscisic acid-dependent response to drought. Plant Cell Environ. 43, 2239–2253 (2020). · DOI
- Zhang, C. et al. The Overexpression of Zea mays Strigolactone Receptor Gene D14 Enhances Drought Resistance in Arabidopsis thaliana L. Int. J. Mol. Sci. 25, 1327 (2024). · DOI
- Niu, K. et al. Cadmium stress suppresses the tillering of perennial ryegrass and is associated with the transcriptional regulation of genes controlling axillary bud outgrowth. Ecotoxicol. Environ. Saf. 212, 112002 (2021). · DOI
- Hu, Z. et al. Strigolactone and cytokinin act antagonistically in regulating rice mesocotyl elongation in darkness. Plant Cell Physiol. 55, 30–41 (2014). · DOI
- Lin, H. et al. DWARF27, an iron-containing protein required for the biosynthesis of strigolactones, regulates rice tiller bud outgrowth. Plant Cell 21, 1512–1525 (2009). · DOI · Paper page
- Gulyás, Z. et al. D27-LIKE1 carotenoid isomerase has a preference towards trans/cis and cis/cis conversions in Arabidopsis. bioRxiv, 2022.2004. 2006.487258 (2022). · doi:10.1101/2022.04.06.487258
- Tolnai, Z., Sharma, H. & Soós, V. D27-like carotenoid isomerases: At the crossroads of strigolactone and abscisic acid biosynthesis. J. Exp. Bot. 75, 1148–1158 (2024). · DOI
- Sun, H. et al. Strigolactones are involved in phosphate-and nitrate-deficiency-induced root development and auxin transport in rice. J. Exp. Bot. 65, 6735–6746 (2014). · DOI · Paper page
- Hu, J., Chen, G., Xu, K. & Wang, J. Cadmium in cereal crops: Uptake and transport mechanisms and minimizing strategies. J. Agric. Food Chem. 70, 5961–5974 (2022). · DOI
- Hasan, M. N. et al. Genome wide analysis of the heavy-metal-associated (HMA) gene family in tomato and expression profiles under different stresses. Gene 835, 146664 (2022). · DOI
- Li, N. et al. Genome-wide analysis and expression profiling of the HMA gene family in Brassica napus under cd stress. Plant Soil 426, 365–381 (2018). · DOI
- Ahmad, M. Z. et al. Genome wide analysis of HMA gene family in Hydrangea macrophylla and characterization of HmHMA2 in response to aluminum stress. Plant Physiol. Biochem. 216, 109182 (2024). · DOI
- Memon, A. R. In Contaminants in Agriculture: Sources Impacts and Management (Springer, 2020).
- Moravčíková, D. & Žiarovská, J. The effect of cadmium on plants in terms of the response of gene expression level and activity. Plants 12, 1848 (2023). · DOI
- Qiao, K., Gong, L., Tian, Y., Wang, H. & Chai, T. The metal-binding domain of wheat heavy metal ATPase 2 (TaHMA2) is involved in zinc/cadmium tolerance and translocation in Arabidopsis. Plant Cell Rep. 37, 1343–1352 (2018). · DOI
- Zhu, J. et al. 1Selenium supply alters the subcellular distribution and chemical forms of cadmium and the expression of transporter genes involved in cadmium uptake and translocation in winter wheat (Triticum aestivum). BMC Plant Biol. 20, 550 (2020). · DOI
- Sayyadi, G., Niknezhad, Y. & Fallah, H. Sodium nitroprusside ameliorates lead toxicity in rice (Oryza sativa L.) by modulating the antioxidant scavenging system, nitrogen metabolism, lead sequestration mechanism, and proline metabolism. Environ. Sci. Pollut. Res. 30, 24408–24423 (2023). · doi:10.1007/s11356-022-23913-w
- Niekerk, L. A. et al. Heavy metal stress and mitogen activated kinase transcription factors in plants: Exploring heavy metal-ROS influences on plant signalling pathways. Plant Cell Environ. 47, 2793–2810 (2024). · DOI
- Baoxiang, W. et al. A pervasive phosphorylation cascade modulation of plant transcription factors in response to abiotic stress. Planta 258, 73 (2023). · DOI
- Huang, T.-L. & Huang, H.-J. ROS and CDPK-like kinase-mediated activation of MAP kinase in rice roots exposed to lead. Chemosphere 71, 1377–1385 (2008). · DOI
- Muhammad, T. et al. Overexpression of a mitogen-activated protein kinase SlMAPK3 positively regulates tomato tolerance to cadmium and drought stress. Molecules 24, 556 (2019). · DOI
- Mondal, S. Heavy metal stress–induced activation of mitogen-activated protein kinase signalling cascade in plants. Plant Mol. Biol. Rep. 41, 15–26 (2023).
- Navarro, C., Navarro, M. A. & Leyva, A. Arsenic perception and signaling: The yet unexplored world. Front. Plant Sci. 13, 993484 (2022). · DOI
- Zhang, X. et al. Hydrogen peroxide is involved in strigolactone induced low temperature stress tolerance in rape seedlings (Brassica rapa L.). Plant Physiol. Biochem. 157, 402–415 (2020). · doi:10.1016/j.plaphy.2020.11.006
- Abe, S. et al. Carlactone is converted to carlactonoic acid by MAX1 in Arabidopsis and its methyl ester can directly interact with AtD14 in vitro. Proc. Natl. Acad. Sci. USA 111, 18084–18089 (2014). · DOI · Paper page
- Wang, L. et al. Genome-wide identification of MAXs genes for strigolactones synthesis/signaling in solanaceous plants and analysis of their potential functions in tobacco. PeerJ 11, e14669 (2023). · DOI
- Li, X. et al. AtMYBS1 negatively regulates heat tolerance by directly repressing the expression of MAX1 required for strigolactone biosynthesis in Arabidopsis. Plant Commun. 4(6), 100675 (2023). · DOI
- Ünlü, E. S. et al. Identification and expressional profiling of putative MAX1 gene in sugar beet (Beta vulgaris L.). Turk. J. Bot. 44, 377–387 (2020). · doi:10.3906/bot-2002-33
- Castillo, M.-C., Coego, A., Costa-Broseta, Á. & León, J. Nitric oxide responses in Arabidopsis hypocotyls are mediated by diverse phytohormone pathways. J. Exp. Bot. 69, 5265–5278 (2018). · DOI
- Li, G. D. et al. Strigolactones are involved in sugar signaling to modulate early seedling development in Arabidopsis. Plant Biotechnol. 33, 87–97 (2016). · DOI
- Nisa, Z.-U. et al. Strigolactone signaling gene from soybean GmMAX2a enhances the drought and salt-alkaline resistance in Arabidopsis via regulating transcriptional profiles of stress-related genes. Funct. Integr. Genomics 23, 216 (2023). · DOI
Metadata
- Authors
- Ucar, S., Yuce, M., Yigider, E., Aydin, M., Turan, M., Ekinci, M., Ilhan, E., Kasapoglu, A. G., Akca, M., Oztemiz, F., Agar, G., & Yildirim, E.
- Venue
- Scientific Reports
- Published
- 2025-10-30
- Volume
- 15
- Issue
- 1
- ISSN
- 2045-2322
- Cited by
- 3
- References
- 2
- Language
- en
- Licence
- creativecommons.org/licenses/by-nc-nd/4.0 (tdm)
- creativecommons.org/licenses/by-nc-nd/4.0 (vor)
- Funders
- Atatürk University, Scientific Research Projects Coordination Unit (FKP-2023-12238)
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- CoChat. (2026). Citation check: Ameliorative effects of strigolactone on tolerance to lead stress on lettuce (Lactuca sativa L.) plants. https://app.cochat.ai/papers/10.1038/s41598-025-21800-1
- The paper
- Ucar, S., Yuce, M., Yigider, E., Aydin, M., Turan, M., Ekinci, M., Ilhan, E., Kasapoglu, A. G., Akca, M., Oztemiz, F., Agar, G., & Yildirim, E. (2025). Ameliorative effects of strigolactone on tolerance to lead stress on lettuce (Lactuca sativa L.) plants. Scientific Reports. https://doi.org/10.1038/s41598-025-21800-1
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