Please wait a minute...
浙江大学学报（农业与生命科学版）
浙江大学学报(农业与生命科学版)  2014, Vol. 40 Issue (6): 605-610    DOI: 10.3785/j.issn.1008-9209.2014.03.131
生物科学与技术     
Ca2+信号通路对本氏烟叶位介导的核盘菌抗性的影响
吕琳慧1, 徐幼平2, 任至玄1, 康冬1, 王继鹏1, 蔡新忠1*
（1.浙江大学农业与生物技术学院生物技术研究所,杭州310058;2.浙江大学分析测试中心,杭州310058）
Effect of Ca2+ signaling pathway on leaf position-associated resistance to Sclerotinia sclerotiorum in Nicotiana benthamiana.
Lü Linhui1, Xu Youping2, Ren Zhixuan1, Kang Dong1, Wang Jipeng1, Cai Xinzhong1*
(1. Institute of Biotechnology, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310058, China; 2. Centre of Analysis and Measurement, Zhejiang University, Hangzhou 310058, China)
 全文: PDF(8284 KB)   HTML ( ) 
摘要： 组合采用药理学、分子生物学和反向遗传学等技术,分析叶位对本氏烟抗核盘菌（Sclerotinia sclerotiorum）的影响及其机制.结果表明,叶位显著影响本氏烟对核盘菌的抗性,随着叶位自上而下,该抗性逐渐增强.药理学分析结果显示,Ca2+通道抑制剂LaCl3和NaVO3处理消除了本氏烟叶片对核盘菌抗性的叶位间差异.定量反转录聚合酶链反应检测结果显示,3个Ca2+信号通路基因NbCNGC20、NbCAMTA3和NbCML1在本氏烟不同叶位叶片中的表达存在显著差异,随着叶位自上而下逐渐增加.病毒诱导的基因沉默（virus-induced gene silencing,VIGS）分析结果表明,钙调素类似蛋白基因NbCML1的沉默导致叶位介导的本氏烟对核盘菌抗病性的丧失.这些结果说明叶位对本氏烟抗核盘菌具有显著影响,揭示了包括NbCML1基因在内的Ca2+信号通路对叶位介导的核盘菌抗性的重要调控作用.
Abstract: Leaf position significantly affects plant disease resistance. The majority of known examples demonstrate that plants are generally more susceptible to disease in lower leaves than upper leaves. Among them there are the resistances of cabbage to Hyaloperonospora parasitica, tomato to Phytophthora infestans and adlay to Bipolaris coicis. The exception is grapevine-Uncinula necator pathosystem where the lower leaves show a higher resistance to powdery mildew pathogen U. necator than the upper leaves. To date, the molecular mechanisms controlling leaf position-associated resistance remain unclear. Sclerotinia sclerotiorum (Lib.) de Bary is one of the most destructive plant pathogenic fungi in the world. The white mould/stem rot disease caused by S. sclerotiorum is a serious world-wide problem, resulting in a huge yield loss every year. On the other hand, the role of Ca2+ signaling pathway in plant disease resistance has been revealed. Nevertheless, whether it affects the leaf position-associated resistance is still unclear. The aim of this study was to investigate the effect of leaf position on resistance of Nicotiana benthamiana to S. sclerotiorum and to further reveal the role of Ca2+ signaling pathway in this leaf position-associated resistance and thus to improve the understanding of the molecular mechanisms underlying this resistance. The effect of leaf position on the resistance of N. benthamiana to S. sclerotiorum was analyzed by comparison among the resistance of leaves at various positions in the same plants, which was evaluated through inoculation experiments. Contribution of Ca2+ signaling pathway to this leaf position-associated resistance was demonstrated through three layers of assays, pharmacological assay to make clear effect of Ca2+ channel inhibitors LaCl3 and NaVO3 on leaf position-associated resistance, quantitative reverse transcriptase-polymerase chain reaction (qRT-PCR) assay to probe the expression of three Ca2+ signaling-related genes NbCNGC20, NbCAMTA3 and NbCML1 in leaves at different positions and virus-induced gene silencing (VIGS) assay to explore the effect of the Ca2+ signaling-related gene NbCML1 on leaf position-associated resistance to S. sclerotiorum in N. benthamiana. The results of inoculation experiments showed that the leaf position significantly influenced the resistance of N. benthamiana to S. sclerotiorum. The upper, middle and lower leaves of 12-leaf-stage plants formed lesions of 18.0 mm, 13.7 mm and 11.9 mm at diameter, respectively. This demonstrates that the resistance increases in leaves of positions from upper to lower, which is in contrast to most of the reported pathosystems. When pre-infiltrated with 1 mmol/L LaCl3 and 50 μmol/L NaVO3, leaves at different positions exhibited lesions of larger size in comparison with those of the untreated control plants, indicating that the two inhibitors of Ca2+ signaling eliminate the leaf position-associated resistance to S. sclerotiorum in N. benthamiana. Additionally, the expression of genes NbCNGC20, NbCAMTA3 and NbCML1 varied obviously in leaves at different positions, and all of them were increased from upper to lower leaves. Moreover, in NbCML1-silenced plants, all leaves of different positions displayed lesions of larger size, when compared with those of the non-silenced control plants, revealing that the silencing of NbCML1 in N. benthamiana erases the leaf position-associated resistance to S. sclerotiorum. In summary, the data of this study reveal that leaf position significantly affects the resistance of N. benthamiana to S. sclerotiorum. In contrast to most of the reported pathosystems, this resistance is much stronger in lower leaves than in upper ones. Our finding demonstrates that the magnitude trend of leaf position-associated resistance in leaves of various positions is pathosystem-dependent. Furthermore, this study unveils that Ca2+ signaling pathway, including NbCML1, makes great contribution to the leaf position-associated resistance to S. sclerotiorum in N. benthamiana. This finding provides new insights into molecular mechanisms underlying the leaf position-associated resistance.
出版日期: 2014-11-20
CLC:  Q 78  
服务　　
把本文推荐给朋友
加入引用管理器
E-mail Alert
RSS
作者相关文章　　
吕琳慧1
徐幼平2
任至玄1
康冬1
王继鹏1
蔡新忠1*

引用本文:

吕琳慧1, 徐幼平2, 任至玄1, 康冬1, 王继鹏1, 蔡新忠1*. Ca2+信号通路对本氏烟叶位介导的核盘菌抗性的影响[J]. 浙江大学学报(农业与生命科学版), 2014, 40(6): 605-610.

Lü Linhui1, Xu Youping2, Ren Zhixuan1, Kang Dong1, Wang Jipeng1, Cai Xinzhong1*. Effect of Ca2+ signaling pathway on leaf position-associated resistance to Sclerotinia sclerotiorum in Nicotiana benthamiana.. Journal of Zhejiang University (Agriculture and Life Sciences), 2014, 40(6): 605-610.

链接本文:

http://www.zjujournals.com/agr/CN/10.3785/j.issn.1008-9209.2014.03.131    或    http://www.zjujournals.com/agr/CN/Y2014/V40/I6/605

[1] 张永亮， 武安泉， 赵锦慧. 野桑蚕丝氨酸蛋白酶样蛋白基因克隆及特征（英文）[J]. 浙江大学学报(农业与生命科学版), 2014, 40(2): 119-124.
[2] 李阳1， 赵媛1， 徐幼平2， 王继鹏1， 蔡新忠1*. 草酸对植物体内Ca2+浓度及信号传导途径的影响[J]. 浙江大学学报(农业与生命科学版), 2014, 40(2): 141-145.
[3] 张健慧， 王首锋*. 膜荚黄芪苯丙氨酸解氨酶基因在毕赤酵母中的分泌表达[J]. 浙江大学学报(农业与生命科学版), 2014, 40(1): 1-8.
[4] 王家庆1*， 边佳2， 李代宗3， 马爽1， 王亮1， 那广宁1. 虹鳟Ndufb2基因全长cDNA序列的克隆与分析[J]. 浙江大学学报(农业与生命科学版), 2013, 39(6): 600-606.
[5] 王亚1,2， 刘建平1， 徐梦云1， 季为捷1， 凃巨民1， 张晓波1*. 水稻泛素缀合酶样蛋白基因OsCROC-1A的克隆与表达分析[J]. 浙江大学学报(农业与生命科学版), 2013, 39(04): 360-368.
[6] 王安可， 何秋伶， 潘晶晶， 孙英超， 祝水金， 陈进红*. 农杆菌介导的VgDGAT1a基因棉花茎尖转化体系优化研究[J]. 浙江大学学报(农业与生命科学版), 2013, 39(3): 253-260.
[7] . 人辅脂酶样3基因hCLPSL3及其同源基因cDNA克隆及鉴定[J]. 浙江大学学报(农业与生命科学版), 2012, 38(5): 575-584.
[8] . 番茄SlMAPK12基因的分离及表达特征分析[J]. 浙江大学学报(农业与生命科学版), 2012, 38(5): 551-558.