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Single-base resolution methylome of cotton cytoplasmic male sterility system reveals epigenomic changes in response to high-temperature stress during anther development. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1093\/jxb\/erz470\">Journal of Experimental Botany<\/ext-link><\/i> 71:951\u2212969<\/p>","DOI":"10.1093\/jxb\/erz470"},{"key":"key-10.48130\/forres-0026-0025-39","doi-asserted-by":"publisher","unstructured":"<p>Duan W, Yang C, Cao X, Wei C, Chen K, et al. 2023. Chilling-induced peach flavor loss is associated with expression and DNA methylation of functional genes. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1016\/j.jare.2022.12.003\">Journal of Advanced Research<\/ext-link><\/i> 53:17\u221231<\/p>","DOI":"10.1016\/j.jare.2022.12.003"},{"key":"key-10.48130\/forres-0026-0025-40","doi-asserted-by":"publisher","unstructured":"<p>Niederhuth CE, Bewick AJ, Ji L, Alabady MS, Do Kim K, et al. 2016. Widespread natural variation of DNA methylation within angiosperms. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1186\/s13059-016-1059-0\">Genome Biology<\/ext-link><\/i> 17:194<\/p>","DOI":"10.1186\/s13059-016-1059-0"},{"key":"key-10.48130\/forres-0026-0025-41","doi-asserted-by":"publisher","unstructured":"<p>Hofmeister BT, Denkena J, Colom\u00e9-Tatch\u00e9 M, Shahryary Y, Hazarika R, et al. 2020. A genome assembly and the somatic genetic and epigenetic mutation rate in a wild long-lived perennial <i>Populus trichocarpa<\/i>. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1186\/s13059-020-02162-5\">Genome Biology<\/ext-link><\/i> 21:259<\/p>","DOI":"10.1186\/s13059-020-02162-5"},{"key":"key-10.48130\/forres-0026-0025-42","doi-asserted-by":"publisher","unstructured":"<p>Kosov\u00e1 V, Latzel V, Hadincov\u00e1 V, M\u00fcnzbergov\u00e1 Z. 2022. Effect of DNA methylation, modified by 5-azaC, on ecophysiological responses of a clonal plant to changing climate. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1038\/s41598-022-22125-z\">Scientific Reports<\/ext-link><\/i> 12:17262<\/p>","DOI":"10.1038\/s41598-022-22125-z"},{"key":"key-10.48130\/forres-0026-0025-43","doi-asserted-by":"publisher","unstructured":"<p>Tiwari M, Kumar R, Subramanian S, Doherty CJ, Jagadish SVK. 2023. Auxin\u2013cytokinin interplay shapes root functionality under low-temperature stress. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1016\/j.tplants.2022.12.004\">Trends in Plant Science<\/ext-link><\/i> 28:447\u2212459<\/p>","DOI":"10.1016\/j.tplants.2022.12.004"},{"key":"key-10.48130\/forres-0026-0025-44","doi-asserted-by":"publisher","unstructured":"<p>Sato H, Mizoi J, Shinozaki K, Yamaguchi-Shinozaki K. 2024. Complex plant responses to drought and heat stress under climate change. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1111\/tpj.16612\">The Plant Journal<\/ext-link><\/i> 117:1873\u22121892<\/p>","DOI":"10.1111\/tpj.16612"},{"key":"key-10.48130\/forres-0026-0025-45","doi-asserted-by":"publisher","unstructured":"<p>Li B, Liu HT, Sun DY, Zhou RG. 2004. Ca<sup>2+<\/sup> and calmodulin modulate DNA-binding activity of maize heat shock transcription factor <i>in vitro<\/i>. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1093\/pcp\/pch074\">Plant &amp; Cell Physiology<\/ext-link><\/i> 45:627\u2212634<\/p>","DOI":"10.1093\/pcp\/pch074"},{"key":"key-10.48130\/forres-0026-0025-46","doi-asserted-by":"publisher","unstructured":"<p>Zhang W, Zhou RG, Gao YJ, Zheng SZ, Xu P, et al. 2009. Molecular and genetic evidence for the key role of <i>AtCaM3<\/i> in heat-shock signal transduction in <i>Arabidopsis<\/i>. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1104\/pp.108.133744\">Plant Physiology<\/ext-link><\/i> 149:1773\u22121784<\/p>","DOI":"10.1104\/pp.108.133744"},{"key":"key-10.48130\/forres-0026-0025-47","doi-asserted-by":"publisher","unstructured":"<p>Franklin KA, Lee SH, Patel D, Kumar SV, Spartz AK, et al. 2011. Phytochrome-interacting factor 4 (PIF4) regulates auxin biosynthesis at high temperature. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1073\/pnas.1110682108\">Proceedings of the National Academy of Sciences of the United States of America<\/ext-link><\/i> 108:20231\u221220235<\/p>","DOI":"10.1073\/pnas.1110682108"},{"key":"key-10.48130\/forres-0026-0025-48","doi-asserted-by":"publisher","unstructured":"<p>Mao Z, He S, Xu F, Wei X, Jiang L, et al. 2020. Photoexcited CRY1 and phyB interact directly with ARF6 and ARF8 to regulate their DNA-binding activity and auxin-induced hypocotyl elongation in <i>Arabidopsis<\/i>. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1111\/nph.16194\">New Phytologist<\/ext-link><\/i> 225:848\u2212865<\/p>","DOI":"10.1111\/nph.16194"},{"key":"key-10.48130\/forres-0026-0025-49","doi-asserted-by":"publisher","unstructured":"<p>Ma L, Li X, Zhao Z, Hao Y, Shang R, et al. 2021. Light-Response Bric-A-Brack\/Tramtrack\/Broad proteins mediate cryptochrome 2 degradation in response to low ambient temperature. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1093\/plcell\/koab219\">The Plant Cell<\/ext-link><\/i> 33:3610\u22123620<\/p>","DOI":"10.1093\/plcell\/koab219"},{"key":"key-10.48130\/forres-0026-0025-50","doi-asserted-by":"publisher","unstructured":"<p>Choi WG, Toyota M, Kim SH, Hilleary R, Gilroy S. 2014. Salt stress-induced Ca<sup>2+<\/sup> waves are associated with rapid, long-distance root-to-shoot signaling in plants. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1073\/pnas.1319955111\">Proceedings of the National Academy of Sciences of the United States of America<\/ext-link><\/i> 111:6497\u22126502<\/p>","DOI":"10.1073\/pnas.1319955111"},{"key":"key-10.48130\/forres-0026-0025-51","doi-asserted-by":"publisher","unstructured":"<p>Xiong TC, Ronzier E, Sanchez F, Corratg\u00e9-Faillie C, Mazars C, et al. 2014. Imaging long distance propagating calcium signals in intact plant leaves with the BRET-based GFP-aequorin reporter. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.3389\/fpls.2014.00043\">Frontiers in Plant Science<\/ext-link><\/i> 5:43<\/p>","DOI":"10.3389\/fpls.2014.00043"},{"key":"key-10.48130\/forres-0026-0025-52","doi-asserted-by":"publisher","unstructured":"<p>Choi WG, Hilleary R, Swanson SJ, Kim SH, Gilroy S. 2016. Rapid, long-distance electrical and calcium signaling in plants. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1146\/annurev-arplant-043015-112130\">Annual Review of Plant Biology<\/ext-link><\/i> 67:287\u2212307<\/p>","DOI":"10.1146\/annurev-arplant-043015-112130"},{"key":"key-10.48130\/forres-0026-0025-53","doi-asserted-by":"publisher","unstructured":"<p>Toyota M, Spencer D, Sawai-Toyota S, Wang J, Tong Z, et al. 2018. Glutamate triggers long-distance, calcium-based plant defense signaling. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1126\/science.aat7744\">Science<\/ext-link><\/i> 361:1112\u22121115<\/p>","DOI":"10.1126\/science.aat7744"},{"key":"key-10.48130\/forres-0026-0025-54","doi-asserted-by":"publisher","unstructured":"<p>Prerostova S, Rezek J, Jarosova J, Lacek J, Dobrev P, et al. 2023. Cytokinins act synergistically with heat acclimation to enhance rice thermotolerance affecting hormonal dynamics, gene expression and volatile emission. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1016\/j.plaphy.2023.107683\">Plant Physiology and Biochemistry<\/ext-link><\/i> 198:107683<\/p>","DOI":"10.1016\/j.plaphy.2023.107683"},{"key":"key-10.48130\/forres-0026-0025-55","doi-asserted-by":"publisher","unstructured":"<p>Qi X, Shen X, Luo L, Huang S, Yu W, et al. 2026. Mechanism of engineered rhizobia overexpressing cytokinin improve heat stress response in alfalfa. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1111\/pce.70396\">Plant, Cell &amp; Environment<\/ext-link><\/i> 49:2888\u22122904<\/p>","DOI":"10.1111\/pce.70396"},{"key":"key-10.48130\/forres-0026-0025-56","doi-asserted-by":"publisher","unstructured":"<p>Prerostova S, Jaro\u0161ov\u00e1 J, Dobrev P, Gaudinova A, Knirsch V, et al. 2025. Cytokinin elevation caused by high light intensity contributes substantially to the increase of thermotolerance of rice plants. <i><ext-link ext-link-type=\"uri\" xmlns:xlink=\"http:\/\/www.w3.org\/1999\/xlink\" xlink:href=\"https:\/\/doi.org\/10.1016\/j.stress.2025.100904\">Plant Stress<\/ext-link><\/i> 16:100904<\/p>","DOI":"10.1016\/j.stress.2025.100904"}],"container-title":["Forestry Research"],"original-title":[],"deposited":{"date-parts":[[2026,7,31]],"date-time":"2026-07-31T11:20:56Z","timestamp":1785496856000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.maxapress.com\/article\/doi\/10.48130\/forres-0026-0025"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2026]]},"references-count":56,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2026]]}},"URL":"https:\/\/doi.org\/10.48130\/forres-0026-0025","relation":{},"ISSN":["2767-3812"],"issn-type":[{"value":"2767-3812","type":"print"}],"subject":[],"published":{"date-parts":[[2026]]}}}