[1]Rozema J, Boelen P, Blokker P. Depletion of stratospheric ozone over the Antarctic and Arctic: responses of plants of polar terrestrial ecosystems to enhanced UV-B, an overview. Environmental Pollution, 2005, 137: 428-442.[2]Jenkins G I. Signal transduction in responses to UV-B radiation. Annual Review of Plant Biology, 2009, 60: 407-431.[3]Brown B A, Jenkins G I. UV-B Signaling pathways with different fluence-rate response profiles are distinguished in mature arabidopsis leaf tissue by requirement for UVR8, HY5, and HYH. Plant Physiology, 2008: 146: 576-588. [4]Neill S J, Desikan R, Clarke A, Hurst R D, Hancock J T. Hydrogen peroxide and nitric oxide as signalling molecules in plants. Journal of Experimental Botany, 2002, 53: 1237-1247.[5]Desikan R, Cheung M K, Bright J, Henson D, Hancock J T, Neill S J. ABA, hydrogen peroxide and nitric oxide signaling in stomatal guard cells. Journal of Experimental Botany, 2004, 55: 205-212.[6]Khokon M A R, Hossain M A, Munemasa S, Uraji M, Nakamura Y, Mori I C, Murata Y. Yeast elicitor-induced stomatal closure along with peroxidase-mediated ROS production in Arabidopsis. Plant and Cell Physiology, 2010, 51: 1915-1921.[7]An Z F, Jing W, Liu Y L, Zhang W H. Hydrogen peroxide generated by copper amine oxidase is involved in abscisic acid-induced stomatal closure in Vicia faba. Journal of Experimental Botany, 2008, 59: 815-825.[8]Sagi M, Fluhr R. Production of reactive oxygen species by plant NADPH oxidases. Plant Physiology, 2006, 141: 336-340.[9]Wang P, Song C P. Guard-cell signalling for hydrogen peroxide and abscisic acid. New Phytologist, 2008, 178: 703-718.[10]Ulm R, Nagy F. Signaling and gene regulation in response to ultraviolet light. Current Opinion in Plant Biology, 2005, 8: 477-482.[11]Wang Y B, Feng H Y, Qu Y, Cheng J Q, Zhao Z G, Zhang M X, Wang X L, An L Z. The relationship between reactive oxygen species and nitric oxide in ultraviolet-B-induced ethylene production in leaves of maize seedlings. Environmental and Experimental Botany, 2006, 57: 51-61.[12]Mackerness S A H, John C F, Jordan B, Thomas B. Early signaling components in ultraviolet-B responses: distinct roles for different reactive oxygen species and nitric oxide. FEBS Letters, 2001, 489: 237-242.[13]He J M, Xu H, She X P, Song X G, Zhao W M. The role and the interrelationship of hydrogen peroxide and nitric oxide in the UV-B-induced stomatal closure in broad bean. Functional Plant Biology, 2005, 32: 237-247.[14]He J M, Yue X Z, Wang R B, Zhang Y. Ethylene mediates UV-B-induced stomatal closure via peroxidase-dependent hydrogen peroxide synthesis in Vicia faba L. Journal of Experimental Botany, 2011, 62: 2657-2666.[15]He J M, Ma X G, Zhang Y, Sun T F, Xu F F, Chen Y P, Liu X, Yue M. Role and interrelationship of Gα protein, hydrogen peroxide and nitric oxide in UV-B-induced stomatal closure in Arabidopsis leaves. Plant Physiology, 2013, 161: 1570-1583.[16]Toker A, Cantley L C. Signaling through the lipid products of phosphoinositide-3-OH kinase. Nature, 1997, 387: 673-676.[17]Rameh L E, Cantley L C. The role of phosphoinositide 3-kinase lipid products in cell function. Journal of Biological Chemistry, 1999, 274: 8347-8350.[18]Bunney T D, Watkins P A, Beven A F, Shaw P J, Hernandez L E, Lomonossoff G P, Shanks M, Peart J, DrØbak B K. Association of phosphatidylinositol 3-kinase with nuclear transcription sites in higher plants. The Plant Cell, 2000, 12: 1679-1687.[19]Welters P, Takegawa K, Emr S D, Chrispeels M J. ATVPS34, a PtdIns 3-kinase of Arabidopsis thaliana is an essential protein with homology to a calcium-dependent lipid-binding domain. Proceedings of the National Academy of Science of USA, 1994, 91: 11398-11402.[20]Hong Z, Verma D P S. A phosphatidylinositol 3-kinase is induced during soybean nodule organogenesis and is associated with membrane proliferation. Proceedings of the National Academy of Science of USA, 1994, 91: 9617-9621.[21]Kim D H, Eu Y J, Yoo C M, Kim Y W, Pih K T, Jin J B, Kim S J, Stenmark H, Hwang I H. Trafficking of phosphatidylinositol 3-phosphate from the trans-Golgi network to the lumen of the central vacuole in plant cells. The Plant Cell, 2001, 13: 287-301.[22]Thole J M, Nielsen E. Phosphoinositides in plants: novel functions in membrane trafficking. Current Opinion in Plant Biology, 2008, 11: 620-631.[23]Lee Y, Kim E S, Choi Y, Hwang I, Staiger C J, Chung Y Y, Lee Y. The Arabidopsis phosphatidylinositol 3-kinase is important for pollen development. Plant Physiology, 2008, 147: 1886-1897.[24]Lee Y, Bak G, Choi Y, Chuang W I, Cho H T, Lee Y. Roles of phosphatidylinositol 3-kinase in root hair growth. Plant Physiology, 2008, 147: 624-635.[25]Joo J H, Yoo H J, Hwang I, Lee J S, Nam K H, Bae Y S. Auxin-induced reactive oxygen species production requires the activation of phosphatidylinositol 3-kinase. FEBS Letters, 2005, 14: 1243-1248.[26]Leshem Y, Seri L, Levine A. Induction of phosphatidylinositol 3-kinase-mediated endocytosis by salt stress leads to intracellular production of reactive oxygen species and salt tolerance. Plant Journal, 2007, 51: 185-197.[27]Yeh C M, Chien P S, Huang H J. Distinct signalling pathways for induction of MAP kinase activities by cadmium and copper in rice roots. Journal of Experimental Botany, 2007, 58: 659-671.[28]Hung K T, Kao C H. Phosphatidylinositol 3-phosphate is required for abscisic acid-induced hydrogen peroxide production in rice leaves. Plant Growth Regulation, 2005, 45: 95-101.[29]Peleg-Grossman S, Volpin H, Levine A. Root hair curling and Rhizobium infection in Medicago truncatula are mediated by phosphatidylinositide-regulated endocytosis and reactive oxygen species. Journal of Experimental Botany, 2007, 58: 1637-1649.[30]Kale S D, Gu B, Capelluto D G S, Dou D, Feldman E, Rumore A, Arredondo F D, Hanlon R, Fudal I, Rouxel T, Lawrence C B, Shan W, Tyler B M. External lipid PI3P mediates entry of eukaryotic pathogen effectors into plant and animal host cells. Cell, 2010, 142: 284-295.[31]Jung J Y, Kim Y W, Kwak J M, Hwang J U, Young J, Schroeder J I, Hwang I, Lee Y. Phosphatidylinositol 3- and 4-phosphate are required for normal stomatal movements. The Plant Cell, 2002, 14: 2399-2412.[32]Park K Y, Jung J Y, Park J, Hwang J U, Kim Y W, Hwang I, Lee Y. A role for phosphatidylinositol 3-phosphate in abscisic acid-induced reactive oxygen species generation in guard cells. Plant Physiology, 2003, 132: 92-98.[33]Kolla V A, Vavasseur A, Raghavendra A S. Hydrogen peroxide production is an early event during bicarbonate induced stomatal closure in abaxial epidermis of Arabidopsis. Planta, 2007, 225: 1421-1429.[34]Ellson C, Davidson K, Anderson K, Stephens L R, Hawkins P T. PtdIns3P binding to the PX domain of p40phox is a physiological signal in NADPH oxidase activation. The EMBO Journal, 2006, 25: 4468-4478.[35]Zhang Y, Zhu H, Zhang Q, Li M, Yan M, Wang R, Wang L, Welti R, Zhang W, Wang X. Phospholipase Dα1 and phosphatidic acid regulate NADPH oxidase activity and production of reactive oxygen species in ABA-mediated stomatal closure in Arabidopsis. The Plant Cell, 2009, 21: 2357-2377.[36]Krinke O, Ruelland E, Valentová O, Vergnolle C, Renou J-P, Taconnat L. Flemr M, Burketová L, Zachowski A. Phosphatidylinositol 4-kinase activation is an early response to salicylic acid in Arabidopsis suspension cells. Plant Physiology, 2007, 144: 1347-1359. |