收稿日期: 2008-09-01
修回日期: 2009-03-15
网络出版日期: 2009-07-30
基金资助
国家自然科学基金(30470335);国家自然科学基金(30770402);广东省自然科学基(金E039254);广东省自然科学基(30770402);广东省自然科学基金(E039254);广东省自然科学基金(06025813)
TIMING AND CONCENTRATION EFFECTS ON THE DEFENSE RESPONSE OF ZEA MAYS SEEDLINGS AFTER APPLICATION OF JASMONIC ACID TO LEAVES
Received date: 2008-09-01
Revised date: 2009-03-15
Online published: 2009-07-30
茉莉酸是环境胁迫下植物产生防御反应的重要信号物质, 但它发挥生理作用的时间和浓度效应以及该效应在叶片和根系中差异性并不清楚。该文以‘高油115’玉米(Zea mays)为材料, 采用4种浓度(1、2.5、5和10 mmol·L-1)的外源茉莉酸溶液涂施玉米幼苗叶片, 在3~48 h的不同时间内跟踪测定叶片和根系中的直接防御物质(丁布(DIMBOA)和总酚)含量及其合成调控基因(Bx1、Bx9和PAL)、直接防御蛋白调控基因(PR-1、PR-2a和MPI)和间接防御物质挥发物调控基因(FPS和TPS)表达的动态变化。结果表明, 外源茉莉酸处理对玉米叶和根系的化学防御反应具有显著的时间和浓度效应。茉莉酸处理玉米叶片后3~6 h就能诱导叶片中Bx9和PAL基因的表达, 使得丁布和总酚的含量显著增加, 且与处理浓度有呈正比的趋势, 随后诱导作用逐渐减弱; 茉莉酸处理还能明显诱导叶片中PR-2a和MPI基因的表达, 诱导作用分别持续到24和48 h; 在处理后3~6 h内, 高浓度茉莉酸处理对挥发物调控基因FPS表达起诱导作用, 而低浓度茉莉酸则对TPS基因的表达起诱导作用。此外, 茉莉酸处理玉米叶片还能间接影响到根系的防御反应, 但大部分检测指标表明间接诱导作用主要出现在处理后期(24~48 h)。例如, 在处理后48 h, 茉莉酸能系统增加根系中直接防御物质丁布和总酚的含量, 增强根系中防御相关基因PR-2a、MPI、FPS和TPS的表达, 并有随茉莉酸处理浓度的增加而增强的趋势。可见, 外源茉莉酸叶片涂施玉米幼苗对根系的间接诱导作用不如对叶片的直接诱导作用强; 叶片启动防御反应的时间较根系早; 随着处理浓度的增加, 茉莉酸对叶片和根系中防御反应的诱导作用有增强的趋势。
冯远娇, 王建武, 骆世明 . 叶片涂施茉莉酸对玉米幼苗防御反应的时间和浓度效应[J]. 植物生态学报, 2009 , 33(4) : 812 -823 . DOI: 10.3773/j.issn.1005-264x.2009.04.020
Aims Our objectives were to investigate temporal dynamics of the contents of direct defense chemicals (DIMBOA and total phenolics) and the expression levels of their corresponding key genes (Bx1, Bx9 and PAL), direct defense protein-related genes (PR-1, PR-2a and MPI), and indirect defense chemical volatile-related genes (FPS and TPS) in leaves and root systems of Zea mays seedlings under the application of exogenous jasmonic acid (JA) on leaf surface.
Methods Leaves of Z. mays cultivar Gaoyou 115 were treated with JA with concentrations of 1, 2.5, 5 and 10 mmol·L-1. We examined contents of the defense chemicals and expression dynamics of their synjournal-mediated genes, direct defense protein-related genes and indirect defense chemical volatile-related genes in both leaves and roots from 3 to 48 h after the application.
Important findings Exogenous JA application resulted in significant timing and concentration effects on the chemical defense response. Gene expression of Bx9 and PAL in the leaves could be induced 3 to 6 h after treatment, resulting in an apparent increase in the content of DIMBOA and total phenolics. The increase was positively correlated with JA concentrations, but the inductive effect gradually decreased afterward. Gene expression of PR-2a and MPI in the leaves was also dramatically induced by JA up to 24 and 48 h, respectively. High JA concentrations induced the expression of FPS gene, whereas low JA concentrations had inducible effects on the expression of TPS after 3-6 h. In addition, JA treatment to leaves could indirectly induce the defense response in roots. Most parameters measured in the indirect induction mainly occurred in the later phase (after 24-48 h) of the treatment. For example, JA systematically increased the contents of DIMBOA and total phenolics in the roots and enhanced the expression of PR-2a, MPI, FPS and TPS genes in the roots 48 h after the treatment, showing a tendency of positive relationship with JA concentrations. These findings provided evidence that the indirect induction by JA application to Z. mays leaves on roots was not as strong as on leaves. Leaves started the defense response earlier than roots, and the induction of defense response both in leaves and roots was increased with increasing JA concentrations.
Key words: Zea mays; jasmonic acid; induced defense; timing and concentration effects
[1] | Bezemer TM, van Dam NM (2005). Linking aboveground and belowground interactions via induced plant defenses. Trends in Ecology and Evolution, 20, 617-624. |
[2] | Creelman RA, John EM (1997). Oligosaccharins, brassinolides, and jasmonates: nontr-aditional regulators of plant growth, development, and gene expression. Plant Cell, 9, 1211-1223. |
[3] | Erb M, Ton J, Degenhardt J, Turlings TCJ (2008). Interactions between arthropod-induced aboveground and belowground defenses in plants. Plant Physiology, 146, 867-874. |
[4] | Feng YJ (冯远娇), Wang JW (王建武), Luo SM (骆世明) (2007). Effects of exogenous jasmonic acid on concentrations of direct defense chemicals and expression of related genes in Bt (Bacillus thuringiensis) corn (Zea mays). Scientia Agricultura Sinica (中国农业科学), 40, 2481-2487. (in Chinese with English abstract) |
[5] | Gui LY (桂连友), Liu SS (刘树生), Chen ZM (陈宗懋) (2004). Plant resistance to insects induced by application of exogenous jasmonic acid and methyl jasmonate. Acta Entomologica Sinica (昆虫学报), 47, 507-514. (in Chinese with English abstract) |
[6] | Halitschke R, Baldwin IT (2003). Antisense LOX expression increases herbivore performance by decreasing defense responses and inhibiting growth-related transcriptional reorganization in Nicotiana attenuate. The Plant Journal, 36, 794-807. |
[7] | Halitschke R, Baldwin IT (2005). Jasmonates and related compounds in plant-insect interactions. Journal of Plant Growth Regulation, 23, 238-245. |
[8] | Hol WGH, Macel M, van Veen JA, van der Meijden E (2004). Root damage and aboveground herbivory change concentration and composition of pyrrolizidine alkaloids of Senecio jacobaea. Basic and Applied Ecology, 5, 253-260. |
[9] | Howe GA (2005). Jasmonates as signals in the wound response. Journal of Plant Growth Regulation, 23, 223-237. |
[10] | Lichtenthaler HK (1999). The 1-deoxy-d-xylulose-5-phosphate pathway of isoprenoid biosynjournal in plants. Annual Review of Plant Physiology and Plant Molecular Biology, 50, 47-65. |
[11] | Ludwig-Müller J, Schubert B, Pieper K, Ihmig S, Hilgenberg W (1997). Glucosinolate content in susceptible and resistant chinese cabbage varieties during development of clubroot disease. Phytochemistry, 44, 407-417. |
[12] | Lü YB (吕要斌), Liu SS (刘树生) (2004). Effects of plant responses induced by exogenous jasmonic acid on host-selection behavior of Cotesia plutellae (Hymenopters: Braconidae). Acta Entomologica Sinica (昆虫学报), 47, 206-212. (in Chinese with English abstract) |
[13] | Nie CR (聂呈荣), Luo SM (骆世明), Wang JW (王建武), Huang JH (黄京华), Zeng RS (曾任森) (2005). Change in concentration of secondary metabolites- DIMBOA and phenolic acids in leaves of Bt corn. Acta Ecologica Sinica (生态学报), 25, 814-823. (in Chinese with English abstract) |
[14] | Omer AD, Thaler JS, Granett J, karban R (2000). Jasmonic acid induced resistance in grapevines to a root and leaf feeder. Journal of Economic Entomology, 93, 840-845. |
[15] | Pauw B, Memelink J (2005). Jasmonate-responsive gene expression. Journal of Plant Growth Regulation, 23, 200-210. |
[16] | Pe?a-Cortés H, Barrios P, Dorta F, Polanco V, Sánchez C, Sánchez E, Ramírez I (2005). Involvement of jasmonic acid and derivatives in plant responses to pathogens and insects and in fruit ripening. Journal of Plant Growth Regulation, 23, 246-260. |
[17] | Pozo MJ, Van Loon LC, Pieterse CMJ (2005). Jasmonates- signals in plant-microbe interactions. Journal of Plant Growth Regulation, 23, 211-222. |
[18] | Rasmann S, Turlings TCJ (2008). First insights into specificity of belowground tritrophic interactions. Oikos, 117, 362-369. |
[19] | Ryan CA (2000). The systemic signaling pathway: differential activation of plant defensive genes. Biochimica et Biophysica Acta, 1477, 112-121. |
[20] | Saedler R, Baldwin IT (2004). Virus-induced gene silencing of jasmonate―induced direct defences, nicotine and trypsin proteinase-inhibitors in Nicotiana attenuate. Journal of Experimental Botany, 55, 151-157. |
[21] | Schenk PM, Kazan K, Rusu AG, Manners JM, Maclean DJ (2005). The SEN1 gene of Arabidopsis is regulated by signals that link plant defence responses and senescence. Plant Physiology and Biochemistry, 43, 997-1005. |
[22] | Schmelz EA, Alborn HT, Engelberth J, Tumlinson JH (2003). Nitrogen deficiency increases volicitin-induced volatile emission, jasmonic acid accumulation, and ethylene sensitivity in maize. Plant Physiology, 133, 295-306. |
[23] | Soler R, Bezemer TM, Cortesero AM, van der Putten WH, Vet LEM, Harvey JA (2007). Impact of foliar herbivory on the development of a root-feeding insect and its parasitoid. Oecologia, 152, 257-264. |
[24] | Stout MJ, Fidantsef AL, Duffey SS, Bostock RM (1999). Signal interactions in pathogen and insect attack: systemic plant-mediated interactions between pathogens and herbivores of the tomato,Lycopersicon esculentum. Physiological and Molecular Plant Pathology, 54, 115-130. |
[25] | Stratmann JW (2003). Long distance run in the wound response-jasmonic acid is pulling ahead. Trends in Plant Science, 8, 247-250. |
[26] | Thaler JS, Fidantsef AL, Bostock RM (2002). Antagonism between jasmonate- and salicylate-mediated induced plant resistance: effects of concentration and timing of elicitation on defense-related proteins, herbivores, and pathogen performace in tomato. Journal of Chemical Ecology, 28, 1131-1159. |
[27] | van Dam NM, Horn M, Mare? M, Baldwin IT (2001). Ontogeny constrains the systemic proteinase inhibitor response in Nicotiana attenuata. Journal of Chemical Ecology, 27, 547-568. |
[28] | van Dam NM, Witjes L, Svato? A (2004). Interactions between aboveground and belowground induction of lucosinolates in two wild Brassica species. New Phytologist, 161, 801-810. |
[29] | Walters D, Cowley T, Mitchell A (2002). Methyl jasmonate alters polyamine metabolism and induces systemic protection against powdery mildew infection in barley. Journal of Experimental Botany, 53, 747-756. |
[30] | Wang JW, Xu T, Zhang LW, Zhong ZM, Luo SM (2007). Effects of methyl jasmonate on hydroxamic acid and phenolic acid content in maize and its allelopathic activity to Echinochloa crusgalli(L.). Allelopathy Journal, 19, 161-170. |
[31] | Wang XM, Ma QH (2005). Characterization of a jasmonate- regulated wheat protein related to a beta-glucosidase- aggregating factor. Plant Physiology and Biochemistry, 43, 185-192. |
[32] | Wasternack C (2005). Introductory remarks on biosynjournal and diversity in actions. Journal of Plant Growth Regulation, 23, 167-169. |
[33] | Xu T (徐涛), Wang JW (王建武), Luo SM (骆世明) (2005). Cloning of the key genes in maize oxylipins pathways and their roles in herbivore induced defense. Chinese Science Bulletin (科学通报), 50, 2217-2225. (in Chinese with English abstract) |
[34] | Xu T (徐涛), Zhou Q (周强), Chen W (陈威), Zhang GR (张古忍), He GF (何国锋), Gu DX (古德祥), Zhang WQ (张文庆) (2003). Involvement of jasmonate- signaling pathway in the herbivore-induced rice plant defense. Chinese Science Bulletin (科学通报), 48, 1442-1449. (in Chinese with English abstract) |
[35] | Zavala JA, Patankar AG, Gase K, Baldwin IT (2004a). Constitutive and inducible trypsin proteinase inhibitor production incurs large fitness costs in Nicotiana attenuate. Proceedings of the National Academy of Sciences of the United States of America, 101, 1607-1612. |
[36] | Zavala JA, Patankar AG, Gase K, Hui D, Baldwin IT (2004b). Manipulation of endogenous trypsin proteinase inhibitor production inNicotiana attenuata demonstrates their function as antiherbivore defenses. Plant Physiology, 134, 1181-1190. |
[37] | Zhang ZP, Baldwin IT (1997). Transport of (2-14C) jasmonic acid from leaves to roots mimics wound-induced changes in endogenous jasmonic acid pools in Nicotiana sylvestris. Planta, 203, 436-441. |
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