Difference between revisions of "Os02g0110200"
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The rice OsHPL3 gene is also known as CYP74B2 and similar to Hydroperoxide lyase. | The rice OsHPL3 gene is also known as CYP74B2 and similar to Hydroperoxide lyase. | ||
==Annotated Information== | ==Annotated Information== | ||
| + | ===Gene Symbol=== | ||
| + | *'''''Os02g0110200''''' '''''<=>''''' '''''OsHPL3,ABCB14,CYP74B2''''' | ||
===Function=== | ===Function=== | ||
| + | * '''''OsHPL3''''' is a hydroperoxide lyase gene． GLV，the product of OsHPL3，play an important role in the flee resistance to WBPH. | ||
| + | * OsHPL3 encodes a lipid hydroperoxide lyase, CYP74B2, which mediates plant specific defense responses. | ||
| + | * In addition, OsHPL3 plays an important role in normal rice growth and development. [1-4] | ||
| + | * OsHPL3 transcripts are known to be upregulated in response to wounding[2], suggesting that OsHPL3 plays an important role in wound signaling. OsHPL3 is wound-inducible and exclusively expressed in leaves. In contrast, OsHPL1 and OsHPL2 are not wound induced. | ||
| + | * OsHPL3 is the major wound-induced HPL in rice leaves. Interestingly, mutation in OsHPL3 also creates plants with enhanced resistance to bacterial blight and enhanced expression of PR genes[1]. | ||
| − | + | ===Phenotypic analysis=== | |
| − | The loss-of-function mutant hpl3-1 produced disease-resembling lesions spreading through the whole leaves. A biochemical assay revealed that OsHPL3 possesses intrinsic HPL activity, hydrolyzing hydroperoxylinolenic acid to produce GLVs. OsHPL3 positively modulates resistance to the rice brown planthopper, but negatively modulates resistance to the rice striped stem borer. OsHPL3, by affecting the levels of JA, GLVs and other volatiles, modulates rice-specific defense responses against different invaders. OsHPL3 positively modulates the production of GLVs but negatively affects other volatiles and TrypPI activity as well as JA biosynthesis through substrate competition. OsHPL3 acts as a negative regulator of plant resistance to the chewing herbivore SSB, but a positive regulator of defense against the phloem feeder BPH. OsHPL3 also functions in indirect resistance to BPH through attractiveness to Anagrus nilaparvatae, an egg parasitoid of BPH. We propose that OsHPL3 modulates rice direct and indirect defense responses by affecting the levels of JA and GLVs. | + | * The loss-of-function mutant hpl3-1 produced disease-resembling lesions spreading through the whole leaves. A biochemical assay revealed that OsHPL3 possesses intrinsic HPL activity, hydrolyzing hydroperoxylinolenic acid to produce GLVs. OsHPL3 positively modulates resistance to the rice brown planthopper, but negatively modulates resistance to the rice striped stem borer. OsHPL3, by affecting the levels of JA, GLVs and other volatiles, modulates rice-specific defense responses against different invaders. OsHPL3 positively modulates the production of GLVs but negatively affects other volatiles and TrypPI activity as well as JA biosynthesis through substrate competition. OsHPL3 acts as a negative regulator of plant resistance to the chewing herbivore SSB, but a positive regulator of defense against the phloem feeder BPH. OsHPL3 also functions in indirect resistance to BPH through attractiveness to Anagrus nilaparvatae, an egg parasitoid of BPH. We propose that OsHPL3 modulates rice direct and indirect defense responses by affecting the levels of JA and GLVs. [1] |
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===Expression=== | ===Expression=== | ||
| − | + | * Expression levels of OsHPL3 could be significantly enhanced by mechanical wounding，SSB，BPH and WBPH infestation, whereas exogenous hormones JA and SA treatment had no significant effect. | |
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===Evolution=== | ===Evolution=== | ||
| − | + | * OsHPL3 shares limited homology with other HPLs, including OsHPL1, OsHPL2 and an Arabidopsis HPL that modulates biosynthesis of GLVs and JA in Arabidopsis and tobacco. | |
| − | + | * OsHPL3 has intrinsic HPL activity, metabolizing hydroperoxylinolenic acid to produce GLVs in planta. Loss of OsHPL3function results in increased resistance to the chewing herbivore SSB but enhanced susceptibility to the phloem-feeding herbivore BPH. Interestingly, thehpl3-1plants also exhibited increased attractiveness to the BPH parasitoid A. nilaparvatae. | |
| − | + | * These data strongly suggest that, as an HPL, OsHPL3 is an important player in modulating rice direct and indirect defense responses specifically against different invaders by modulating the oxylipin pathway. [1] | |
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==Labs working on this gene== | ==Labs working on this gene== | ||
| − | + | *1, State Key Laboratory of Plant Genomics, National Centre for Plant Gene Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, People’s Republic of China | |
| − | 1, State Key Laboratory of Plant Genomics, National Centre for Plant Gene Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, People’s Republic of China | + | *2, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310029, China, |
| − | 2, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310029, China, | + | *3, National Key Laboratory of Plant Molecular Genetics and National Center of Plant Gene Research, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China, |
| − | 3, National Key Laboratory of Plant Molecular Genetics and National Center of Plant Gene Research, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China, | + | *4, China National Rice Research Institute, 359 Tiyuchang Road, Hangzhou 31006, China, and National Engineering Center for BioChip at Shanghai, Shanghai 201203, China |
| − | 4, China National Rice Research Institute, 359 Tiyuchang Road, Hangzhou 31006, China, and National Engineering Center for BioChip at Shanghai, Shanghai 201203, China | + | *5, Section of Plant Biology, University of California, Davis, California 95616 |
| − | 5, Section of Plant Biology, University of California, Davis, California 95616 | ||
==References== | ==References== | ||
[1] Xiaohong Tong; Jinfeng Qi; Xudong Zhu; Bizeng Mao; Longjun Zeng; Baohui Wang; Qun Li; Guoxin Zhou; Xiaojing Xu; Yonggen Lou; Zuhua He. The rice hydroperoxide lyase OsHPL3 functions in defense responses by modulating the oxylipin pathway. The Plant Journal, 2012, 71(5): 763-775. | [1] Xiaohong Tong; Jinfeng Qi; Xudong Zhu; Bizeng Mao; Longjun Zeng; Baohui Wang; Qun Li; Guoxin Zhou; Xiaojing Xu; Yonggen Lou; Zuhua He. The rice hydroperoxide lyase OsHPL3 functions in defense responses by modulating the oxylipin pathway. The Plant Journal, 2012, 71(5): 763-775. | ||
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[2] E.W. Chehab, G. Raman, J.W. Walley, J.V. Perea, G. Banu, S.Theg, K.Dehesh. Rice HYDROPEROXIDE LYASES with unique expression patterns generate distinct aldehyde signatures in Arabidopsis. Plant Physiology, 2006, 141(1):121-34. | [2] E.W. Chehab, G. Raman, J.W. Walley, J.V. Perea, G. Banu, S.Theg, K.Dehesh. Rice HYDROPEROXIDE LYASES with unique expression patterns generate distinct aldehyde signatures in Arabidopsis. Plant Physiology, 2006, 141(1):121-34. | ||
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[3] Jinfeng Qi, Guoxin Zhou, Lijuan Yang, Matthias Erb, Yanhua Lu, Xiaoling Sun, Jiaan Cheng, and Yonggen Lou. The Chloroplast-Localized Phospholipases Da4anda5 Regulate Herbivore-Induced Direct and Indirect Defenses in Rice. Plant Physiology, 2011, 157(4):1987-99. | [3] Jinfeng Qi, Guoxin Zhou, Lijuan Yang, Matthias Erb, Yanhua Lu, Xiaoling Sun, Jiaan Cheng, and Yonggen Lou. The Chloroplast-Localized Phospholipases Da4anda5 Regulate Herbivore-Induced Direct and Indirect Defenses in Rice. Plant Physiology, 2011, 157(4):1987-99. | ||
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[4] Xiaoqiang Liu, Feng Li, Jiuyou Tang, Weihong Wang, Fengxia Zhang, Guodong Wang, Jinfang Chu, Cunyu Yan, Taoqing Wang, Chengcai Chu*, Chuanyou Li*. Activation of the Jasmonic Acid Pathway by Depletion of the Hydroperoxide Lyase OsHPL3 Reveals Crosstalk between the HPL and AOS Branches of the Oxylipin Pathway in Rice. PLoS One. 2012;7(11):e50089. doi: 10.1371/journal.pone.0050089. Epub 2012 Nov 29. | [4] Xiaoqiang Liu, Feng Li, Jiuyou Tang, Weihong Wang, Fengxia Zhang, Guodong Wang, Jinfang Chu, Cunyu Yan, Taoqing Wang, Chengcai Chu*, Chuanyou Li*. Activation of the Jasmonic Acid Pathway by Depletion of the Hydroperoxide Lyase OsHPL3 Reveals Crosstalk between the HPL and AOS Branches of the Oxylipin Pathway in Rice. PLoS One. 2012;7(11):e50089. doi: 10.1371/journal.pone.0050089. Epub 2012 Nov 29. | ||
==Structured Information== | ==Structured Information== | ||
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| − | [[Category:Genes]] | ||
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| − | [[Category:Oryza Sativa Japonica Group]] | ||
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Latest revision as of 09:25, 14 February 2017
The rice OsHPL3 gene is also known as CYP74B2 and similar to Hydroperoxide lyase.
Contents
Annotated Information
Gene Symbol
- Os02g0110200 <=> OsHPL3,ABCB14,CYP74B2
Function
- OsHPL3 is a hydroperoxide lyase gene． GLV，the product of OsHPL3，play an important role in the flee resistance to WBPH.
- OsHPL3 encodes a lipid hydroperoxide lyase, CYP74B2, which mediates plant specific defense responses.
- In addition, OsHPL3 plays an important role in normal rice growth and development. [1-4]
- OsHPL3 transcripts are known to be upregulated in response to wounding[2], suggesting that OsHPL3 plays an important role in wound signaling. OsHPL3 is wound-inducible and exclusively expressed in leaves. In contrast, OsHPL1 and OsHPL2 are not wound induced.
- OsHPL3 is the major wound-induced HPL in rice leaves. Interestingly, mutation in OsHPL3 also creates plants with enhanced resistance to bacterial blight and enhanced expression of PR genes[1].
Phenotypic analysis
- The loss-of-function mutant hpl3-1 produced disease-resembling lesions spreading through the whole leaves. A biochemical assay revealed that OsHPL3 possesses intrinsic HPL activity, hydrolyzing hydroperoxylinolenic acid to produce GLVs. OsHPL3 positively modulates resistance to the rice brown planthopper, but negatively modulates resistance to the rice striped stem borer. OsHPL3, by affecting the levels of JA, GLVs and other volatiles, modulates rice-specific defense responses against different invaders. OsHPL3 positively modulates the production of GLVs but negatively affects other volatiles and TrypPI activity as well as JA biosynthesis through substrate competition. OsHPL3 acts as a negative regulator of plant resistance to the chewing herbivore SSB, but a positive regulator of defense against the phloem feeder BPH. OsHPL3 also functions in indirect resistance to BPH through attractiveness to Anagrus nilaparvatae, an egg parasitoid of BPH. We propose that OsHPL3 modulates rice direct and indirect defense responses by affecting the levels of JA and GLVs. [1]
Expression
- Expression levels of OsHPL3 could be significantly enhanced by mechanical wounding，SSB，BPH and WBPH infestation, whereas exogenous hormones JA and SA treatment had no significant effect.
Evolution
- OsHPL3 shares limited homology with other HPLs, including OsHPL1, OsHPL2 and an Arabidopsis HPL that modulates biosynthesis of GLVs and JA in Arabidopsis and tobacco.
- OsHPL3 has intrinsic HPL activity, metabolizing hydroperoxylinolenic acid to produce GLVs in planta. Loss of OsHPL3function results in increased resistance to the chewing herbivore SSB but enhanced susceptibility to the phloem-feeding herbivore BPH. Interestingly, thehpl3-1plants also exhibited increased attractiveness to the BPH parasitoid A. nilaparvatae.
- These data strongly suggest that, as an HPL, OsHPL3 is an important player in modulating rice direct and indirect defense responses specifically against different invaders by modulating the oxylipin pathway. [1]
Labs working on this gene
- 1, State Key Laboratory of Plant Genomics, National Centre for Plant Gene Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing, People’s Republic of China
- 2, College of Agriculture and Biotechnology, Zhejiang University, Hangzhou 310029, China,
- 3, National Key Laboratory of Plant Molecular Genetics and National Center of Plant Gene Research, Institute of Plant Physiology and Ecology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, Shanghai 200032, China,
- 4, China National Rice Research Institute, 359 Tiyuchang Road, Hangzhou 31006, China, and National Engineering Center for BioChip at Shanghai, Shanghai 201203, China
- 5, Section of Plant Biology, University of California, Davis, California 95616
References
[1] Xiaohong Tong; Jinfeng Qi; Xudong Zhu; Bizeng Mao; Longjun Zeng; Baohui Wang; Qun Li; Guoxin Zhou; Xiaojing Xu; Yonggen Lou; Zuhua He. The rice hydroperoxide lyase OsHPL3 functions in defense responses by modulating the oxylipin pathway. The Plant Journal, 2012, 71(5): 763-775.
[2] E.W. Chehab, G. Raman, J.W. Walley, J.V. Perea, G. Banu, S.Theg, K.Dehesh. Rice HYDROPEROXIDE LYASES with unique expression patterns generate distinct aldehyde signatures in Arabidopsis. Plant Physiology, 2006, 141(1):121-34.
[3] Jinfeng Qi, Guoxin Zhou, Lijuan Yang, Matthias Erb, Yanhua Lu, Xiaoling Sun, Jiaan Cheng, and Yonggen Lou. The Chloroplast-Localized Phospholipases Da4anda5 Regulate Herbivore-Induced Direct and Indirect Defenses in Rice. Plant Physiology, 2011, 157(4):1987-99.
[4] Xiaoqiang Liu, Feng Li, Jiuyou Tang, Weihong Wang, Fengxia Zhang, Guodong Wang, Jinfang Chu, Cunyu Yan, Taoqing Wang, Chengcai Chu*, Chuanyou Li*. Activation of the Jasmonic Acid Pathway by Depletion of the Hydroperoxide Lyase OsHPL3 Reveals Crosstalk between the HPL and AOS Branches of the Oxylipin Pathway in Rice. PLoS One. 2012;7(11):e50089. doi: 10.1371/journal.pone.0050089. Epub 2012 Nov 29.
