Jasmonic acid (BioDeep_00000000668)

 

Secondary id: BioDeep_00000398564

natural product human metabolite PANOMIX_OTCML-2023 Endogenous BioNovoGene_Lab2019


代谢物信息卡片


Cyclopentaneacetic acid, 3-oxo-2-(2-pentenyl)-, [1R-[1alpha,2beta(Z)]]-

化学式: C12H18O3 (210.1256)
中文名称: (+-)-茉莉酸, 茉莉酸(JA), 茉莉酸, (±)-茉莉酮酸
谱图信息: 最多检出来源 Viridiplantae(plant) 13.23%

分子结构信息

SMILES: C1C(=O)[C@H](C/C=C\CC)[C@@H](CC(O)=O)C1
InChI: InChI=1S/C12H18O3/c1-2-3-4-5-10-9(8-12(14)15)6-7-11(10)13/h3-4,9-10H,2,5-8H2,1H3,(H,14,15)

描述信息

Jasmonic acid is an oxo monocarboxylic acid that is (3-oxocyclopentyl)acetic acid substituted by a (2Z)-pent-2-en-1-yl group at position 2 of the cyclopentane ring. It has a role as a plant metabolite and a member of jasmonates. It is a conjugate acid of a jasmonate(1-). It is an enantiomer of a (+)-jasmonic acid.
Jasmonic acid is a natural product found in Ficus superba, Cleyera japonica, and other organisms with data available.
Jasmonic acid is found in apple. Esters are present in Jasminum grandiflorum (royal jasmine) and are responsible for its odour. Jasmonic acid is a member of the jasmonate class of plant hormones. It is biosynthesized from linolenic acid by the octadecanoid pathway
An oxo monocarboxylic acid that is (3-oxocyclopentyl)acetic acid substituted by a (2Z)-pent-2-en-1-yl group at position 2 of the cyclopentane ring.
Esters are present in Jasminum grandiflorum (royal jasmine) and are responsible for its odour [DFC]
D006133 - Growth Substances > D010937 - Plant Growth Regulators

同义名列表

59 个代谢物同义名

Cyclopentaneacetic acid, 3-oxo-2-(2-pentenyl)-, [1R-[1alpha,2beta(Z)]]-; [1R-[1alpha,2beta(Z)]]-3-Oxo-2-(2-pentenyl)-cyclopentaneacetic acid; Cyclopentaneacetic acid, 3-oxo-2-(2Z)-2-pentenyl-, (1R,2R)- (9CI); Cyclopentaneacetic acid, 3-oxo-2-(2-pentenyl)-, (Z)-trans- (8CI); Cyclopentaneacetic acid, 3-oxo-2-[(2Z)-2-penten-1-yl]-, (1R,2R)-; (-)-1alpha,2beta-3-Oxo-2-(cis-2-pentenyl)cyclopentaneacetic acid; 2-((1S,2S)-3-Oxo -2-((Z)-pent-2-en-1-yl)cyclopentyl)acetic acid; ()-1alpha,2beta-3-Oxo-2-(cis-2-pentenyl)cyclopentaneacetic acid; 2-[(1R,2R)-3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl]acetic acid; {(1R,2R)-3-Oxo-2-[(Z)pent-2-enyl]cyclopent-2-enyl}acetic acid; {(1R,2R)-3-oxo-2-[(2Z)-pent-2-en-1-yl]cyclopentyl}acetic acid; 2-((1R,2R)-2-((Z)-But-2-en-1-yl)-4-oxocyclopentyl)acetic acid; cyclopentaneacetic acid, 3-oxo-2-[(2Z)-2-pentenyl]-, (1R,2R)-; [1R-[1α,2β(Z)]]-3-Oxo-2-(2-pentenyl)-cyclopentaneacetic acid; 2-[(1R,2R)-3-oxo-2-[(Z)-pent-2-enyl]cyclopentyl]acetic acid; Cyclopentaneacetic acid, 3-oxo-2-(2Z)-2-pentenyl-, (1R,2R)-; 2-{(1R,2R)-3-oxo-2-[(Z)-pent-2-enyl]cyclopentyl}acetic acid; 2-[(1R,2R)-2-((2Z)pent-2-enyl)-3-oxocyclopentyl]acetic acid; (1R,2R)-3-Oxo-2-(2Z)-2-penten-1-ylcyclopentaneacetic acid; {(1R,2R)-3-oxo-2-[(Z)pent-2-enyl]cyclopent-2-enyl}acetate; 2-{(1R,2R)-3-oxo-2-[(Z)-pent-2-enyl]cyclopentyl}acetate; (1r,2r)-3-oxo-2-(2z)-2-pentenyl-cyclopentaneacetic acid; (1R,2R)-3-oxo-2-(pent-2Z-enyl)-cyclopentaneacetic acid; (Z)-trans-3-Oxo-2-(2-pentenyl)-cyclopentaneacetic acid; (Z)-2-(2-(but-2-en-1-yl)-4-oxocyclopentyl)-acetic acid; (1R,2R)-3-OXO-2-(2Z)-2-PENTENYLCYCLOPENTANEACETIC ACID; (1R,2R)-3-oxo-2-(2Z)-2-penten-ylcyclopentanacetic acid; (1R,2R)-3-OXO-2-(Z)-PENT-2-ENYLCYCLOPENTYLACETIC ACID; 3-oxo-2R-(2Z)2-penten-1R-yl-cyclopentaneacetic acid; (1R,2R)-3-oxo-2-(Pent-2Z-enyl)-cyclopentaneacetate; 3-Oxo-2R-(2Z)2-penten-1R-ylcyclopentaneacetic acid; (1R,2R)-3-oxo-2-(2Z)-2-Penten-ylcyclopentanacetate; 3-Oxo-2-(2-pentenyl)cyclopentaneacetic acid; 3-Oxo-2-(2Z-pentenyl)cyclotentylacetic acid; trans-Jasmonic Acid (1 g/ 10 mL Ethanol); E9BF63E8-55FE-4051-AE00-04B002D8CE1F; (3R,7R)-(?)-Jasmonic acid; (3R,7R)(-)-Jasmonic acid; (1R,2R)-Jasmonic acid; (3R,7R)-Jasmonic acid; (+/-)-Jasmonic acid; trans-Jasmonic Acid; 7-epi-jasmonic acid; JASMONIC ACID [MI]; trans-JasmonicAcid; (-)-Jasmonic acid; (±)-Jasmonic acid; ()-Jasmonic acid; UNII-6RI5N05OWW; Jasmonic acid; (-)-jasmonate; 6RI5N05OWW; jasmonate; FA 12:3;O; JA; 3-(Carboxymethyl)-2-(2-pentenyl)cyclopentanone; (+-)-Jasmonic acid; Jasmonic acid; (-)-Jasmonic acid



数据库引用编号

36 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

BioCyc(0)

PlantCyc(0)

代谢反应

4 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(3)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(1)

  • Jasmonic Acid Biosynthesis: 8-[(1R,2R)-3-oxo-2-{(Z)-pent-2-enyl}cyclopentyl]octanoate + Adenosine triphosphate + Coenzyme A ⟶ 3-oxo-2-(cis-2'-pentenyl)-cyclopentane-1-octanoyl-CoA + Adenosine monophosphate + Pyrophosphate

PharmGKB(0)

101 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 9 CAT, GGPS1, HBS1L, HPGDS, PRKN, SKP1, TERF1, ZMYND8, ZNF346
Peripheral membrane protein 2 CYP1B1, PRTN3
Endoplasmic reticulum membrane 3 CYP1B1, DAD1, HSP90B1
Nucleus 8 GTF3A, HSP90B1, MYB, PRKN, SKP1, TERF1, ZMYND8, ZNF346
cytosol 11 CAT, GGPS1, GSR, HBS1L, HPGDS, HSP90B1, LIPE, MYB, PRKN, PRTN3, SKP1
nuclear body 1 TERF1
centrosome 1 SKP1
nucleoplasm 8 GGPS1, GTF3A, HPGDS, MYB, SKP1, TERF1, ZMYND8, ZNF346
RNA polymerase II transcription regulator complex 1 MYB
Cell membrane 2 LIPE, PRTN3
Cytoplasmic granule 1 PRTN3
Multi-pass membrane protein 1 DAD1
cell surface 1 TNFRSF10B
dendritic shaft 1 ZMYND8
Golgi apparatus 2 ATRN, PRKN
smooth endoplasmic reticulum 1 HSP90B1
Cytoplasm, cytosol 2 LIPE, PRKN
Presynapse 1 PRKN
plasma membrane 4 ATRN, NPR1, PRTN3, TNFRSF10B
Membrane 9 CAT, CYP1B1, DAD1, HBS1L, HSP90B1, LIPE, MYB, NPR1, TNFRSF10B
caveola 1 LIPE
extracellular exosome 6 ATRN, CAT, GSR, HBS1L, HSP90B1, PRTN3
endoplasmic reticulum 2 HSP90B1, PRKN
extracellular space 2 ATRN, PRTN3
perinuclear region of cytoplasm 3 GGPS1, HSP90B1, PRKN
mitochondrion 4 CAT, CYP1B1, GSR, PRKN
protein-containing complex 2 CAT, HSP90B1
intracellular membrane-bounded organelle 4 CAT, CYP1B1, HPGDS, PRTN3
Microsome membrane 1 CYP1B1
postsynaptic density 1 PRKN
Single-pass type I membrane protein 1 ATRN
Secreted 1 PRTN3
extracellular region 3 CAT, HSP90B1, PRTN3
Mitochondrion outer membrane 1 PRKN
mitochondrial outer membrane 1 PRKN
[Isoform 2]: Secreted 1 ATRN
mitochondrial matrix 2 CAT, GSR
Extracellular side 1 PRTN3
external side of plasma membrane 1 GSR
dendritic spine 1 ZMYND8
Z disc 1 GGPS1
nucleolus 3 TERF1, ZMYND8, ZNF346
midbody 1 HSP90B1
Cytoplasm, perinuclear region 1 GGPS1
Membrane raft 1 PRTN3
Cytoplasm, cytoskeleton, spindle 1 TERF1
focal adhesion 2 CAT, HSP90B1
spindle 1 TERF1
Peroxisome 1 CAT
Peroxisome matrix 1 CAT
peroxisomal matrix 1 CAT
peroxisomal membrane 1 CAT
collagen-containing extracellular matrix 1 HSP90B1
nuclear speck 1 PRKN
receptor complex 1 NPR1
Cell projection, neuron projection 1 PRKN
neuron projection 1 PRKN
chromatin 1 ZMYND8
Chromosome 2 TERF1, ZMYND8
Nucleus, nucleolus 1 ZNF346
Chromosome, telomere 1 TERF1
chromosome, telomeric region 1 TERF1
[Isoform 3]: Secreted 1 ATRN
fibrillar center 1 TERF1
Lipid droplet 1 LIPE
Membrane, caveola 1 LIPE
Melanosome 1 HSP90B1
sperm plasma membrane 1 HSP90B1
ubiquitin ligase complex 1 PRKN
Cytoplasm, myofibril, sarcomere, Z line 1 GGPS1
plasma membrane raft 1 PRTN3
ficolin-1-rich granule lumen 1 CAT
secretory granule lumen 1 CAT
endoplasmic reticulum lumen 1 HSP90B1
nuclear matrix 1 MYB
PcG protein complex 1 SKP1
azurophil granule lumen 1 PRTN3
aggresome 1 PRKN
nuclear telomere cap complex 1 TERF1
[Isoform 2]: Cytoplasm 1 HBS1L
Sarcoplasmic reticulum lumen 1 HSP90B1
[Isoform 1]: Cell membrane 1 ATRN
dopaminergic synapse 1 PRKN
Lewy body 1 PRKN
Parkin-FBXW7-Cul1 ubiquitin ligase complex 1 PRKN
cytosolic ribosome 1 HBS1L
site of DNA damage 1 ZMYND8
endocytic vesicle lumen 1 HSP90B1
catalase complex 1 CAT
oligosaccharyltransferase complex 1 DAD1
endoplasmic reticulum chaperone complex 1 HSP90B1
SCF ubiquitin ligase complex 1 SKP1
ANPR-A receptor complex 1 NPR1
shelterin complex 1 TERF1
Cul7-RING ubiquitin ligase complex 1 SKP1
Dom34-Hbs1 complex 1 HBS1L


文献列表

  • Tianming Li, Wenjing Jia, Song Peng, Yanhui Guo, Jinrui Liu, Xue Zhang, Panyu Li, Hanfeng Zhang, Ruqiang Xu. Endogenous cAMP elevation in Brassica napus causes changes in phytohormone levels. Plant signaling & behavior. 2024 Dec; 19(1):2310963. doi: 10.1080/15592324.2024.2310963. [PMID: 38314783]
  • Ting Wu, Wen-Jing Wang, Zhou-Yuan Li, Yi-Tian Liu, Tian-Ping Yu, Shuang-Ge Li, Hong-Zhi Du, Chun Gui, Da-Hui Liu, Xiao-Long Yang. Anti-inflammatory discovery of sesquiterpenoids and a jasmonic acid derivative from Artemisia stolonifera. Phytochemistry. 2024 Jul; 223(?):114120. doi: 10.1016/j.phytochem.2024.114120. [PMID: 38705265]
  • Rina Saito, Mai Morikawa, Toshiya Muto, Sayaka Saito, Takuya Kaji, Minoru Ueda. SlCYP94B18 and SlCYP94B19 monooxygenases for the catabolic turnover of jasmonates in tomato leaves. Phytochemistry. 2024 Jul; 223(?):114141. doi: 10.1016/j.phytochem.2024.114141. [PMID: 38750708]
  • Shanwei Wang, Wei Xing, Wei Li, Zuoming Xie, Yuan Xiao, Wenmin Huang. Red light mitigates Cd toxicity in Egeria densa by restricting Cd accumulation and modulating antioxidant defense system. Plant physiology and biochemistry : PPB. 2024 Jun; 211(?):108675. doi: 10.1016/j.plaphy.2024.108675. [PMID: 38705047]
  • Haodong Huang, Yang Wang, Pingfang Yang, Huayan Zhao, Matthew A Jenks, Shiyou Lü, Xianpeng Yang. The Arabidopsis cytochrome P450 enzyme CYP96A4 is involved in the wound-induced biosynthesis of cuticular wax and cutin monomers. The Plant journal : for cell and molecular biology. 2024 Jun; 118(5):1619-1634. doi: 10.1111/tpj.16701. [PMID: 38456566]
  • Yuanyuan Wu, Ying Sun, Wanmin Wang, Zizhao Xie, Chenghang Zhan, Liang Jin, Junli Huang. OsJAZ10 negatively modulates the drought tolerance by integrating hormone signaling with systemic electrical activity in rice. Plant physiology and biochemistry : PPB. 2024 Jun; 211(?):108683. doi: 10.1016/j.plaphy.2024.108683. [PMID: 38714129]
  • Wenliang Li, Wen Liu, Zewei Xu, Chengluo Zhu, Danlu Han, Jianwei Liao, Kun Li, Xiaoyan Tang, Qi Xie, Chengwei Yang, Jianbin Lai. Heat-induced SUMOylation differentially affects bacterial effectors in plant cells. The Plant cell. 2024 May; 36(6):2103-2116. doi: 10.1093/plcell/koae049. [PMID: 38445983]
  • Shotaro Hirota, Yusuke Ito, Shiro Inoue, Naoki Kitaoka, Tohru Taniguchi, Kenji Monde, Kosaku Takahashi, Hideyuki Matsuura. Isolation and Structure Determination of cis-OPDA-α-Monoglyceride from Arabidopsis thaliana. Journal of natural products. 2024 May; 87(5):1358-1367. doi: 10.1021/acs.jnatprod.3c01237. [PMID: 38656153]
  • Yi-Wen Wang, Savithri U Nambeesan. Ethylene promotes fruit ripening initiation by downregulating photosynthesis, enhancing abscisic acid and suppressing jasmonic acid in blueberry (Vaccinium ashei). BMC plant biology. 2024 May; 24(1):418. doi: 10.1186/s12870-024-05106-4. [PMID: 38760720]
  • Ishfaq Majid Hurrah, Amit Kumar, Nazia Abbas. Functional characterisation of Artemisia annua jasmonic acid carboxyl methyltransferase: a key enzyme enhancing artemisinin biosynthesis. Planta. 2024 May; 259(6):152. doi: 10.1007/s00425-024-04433-y. [PMID: 38735012]
  • Vojtěch Schmidt, Roman Skokan, Thomas Depaepe, Katarina Kurtović, Samuel Haluška, Stanislav Vosolsobě, Roberta Vaculíková, Anthony Pil, Petre Ivanov Dobrev, Václav Motyka, Dominique Van Der Straeten, Jan Petrášek. Phytohormone profiling in an evolutionary framework. Nature communications. 2024 May; 15(1):3875. doi: 10.1038/s41467-024-47753-z. [PMID: 38719800]
  • Maria Ladeynova, Darya Kuznetsova, Anna Pecherina, Vladimir Vodeneev. pH change accompanying long-distance electrical signal controls systemic jasmonate biosynthesis. Journal of plant physiology. 2024 May; 296(?):154225. doi: 10.1016/j.jplph.2024.154225. [PMID: 38522214]
  • Cheng Li, Jiancan Du, Huini Xu, Zhenhua Feng, Caspar C C Chater, Yuanwen Duan, Yongping Yang, Xudong Sun. UVR8-TCP4-LOX2 module regulates UV-B tolerance in Arabidopsis. Journal of integrative plant biology. 2024 May; 66(5):897-908. doi: 10.1111/jipb.13648. [PMID: 38506424]
  • Colleen E Fortier, Antonia E Musso, Maya L Evenden, L Irina Zaharia, Janice E K Cooke. Evidence that Ophiostomatoid Fungal Symbionts of Mountain Pine Beetle Do Not Play a Role in Overcoming Lodgepole Pine Defenses During Mass Attack. Molecular plant-microbe interactions : MPMI. 2024 May; 37(5):445-458. doi: 10.1094/mpmi-06-23-0077-r. [PMID: 38240660]
  • Xin Huang, Liyan Su, Baohang Xian, Qiyuan Yu, Miao Zhang, Jie Fan, Chenxi Zhang, Yiqi Liu, Houzheng He, Xin Zhong, Man Li, Shanchun Chen, Yongrui He, Qiang Li. Genome-wide identification and characterization of the sweet orange (Citrus sinensis) basic helix-loop-helix (bHLH) family reveals a role for CsbHLH085 as a regulator of citrus bacterial canker resistance. International journal of biological macromolecules. 2024 May; 267(Pt 2):131442. doi: 10.1016/j.ijbiomac.2024.131442. [PMID: 38621573]
  • Shao-Li Zhou, Jin-Xu Zhang, Shuo Jiang, Yan Lu, Yong-Shuang Huang, Xian-Man Dong, Qin Hu, Wei Yao, Mu-Qing Zhang, Sheng-Hua Xiao. Genome-wide identification of JAZ gene family in sugarcane and function analysis of ScJAZ1/2 in drought stress response and flowering regulation. Plant physiology and biochemistry : PPB. 2024 May; 210(?):108577. doi: 10.1016/j.plaphy.2024.108577. [PMID: 38579542]
  • Zhujuan Guo, Yixin Zuo, Shuyao Wang, Xiao Zhang, Zhaoyuan Wang, Yahui Liu, Yingbai Shen. Early signaling enhance heat tolerance in Arabidopsis through modulating jasmonic acid synthesis mediated by HSFA2. International journal of biological macromolecules. 2024 May; 267(Pt 2):131256. doi: 10.1016/j.ijbiomac.2024.131256. [PMID: 38556243]
  • Rameez Ahmad Khan, Mohammad, Amit Kumar, Nazia Abbas. AaGL3-like is jasmonate-induced bHLH transcription factor that positively regulates trichome density in Artemisia annua. Gene. 2024 Apr; 904(?):148213. doi: 10.1016/j.gene.2024.148213. [PMID: 38281672]
  • Debora Gasperini, Gregg A Howe. Phytohormones in a universe of regulatory metabolites: lessons from jasmonate. Plant physiology. 2024 Apr; 195(1):135-154. doi: 10.1093/plphys/kiae045. [PMID: 38290050]
  • Jaap-Jan Willig, Nina Guarneri, Thomas van Loon, Sri Wahyuni, Ivan E Astudillo-Estévez, Lin Xu, Viola Willemsen, Aska Goverse, Mark G Sterken, José L Lozano-Torres, Jaap Bakker, Geert Smant. Transcription factor WOX11 modulates tolerance to cyst nematodes via adventitious lateral root formation. Plant physiology. 2024 Apr; 195(1):799-811. doi: 10.1093/plphys/kiae053. [PMID: 38330218]
  • Nana Fan, Liantai Su, Aimin Lv, Wuwu Wen, Li Gao, Xiangkai You, Peng Zhou, Yuan An. PECTIN ACETYLESTERASE12 regulates shoot branching via acetic acid and auxin accumulation in alfalfa shoots. Plant physiology. 2024 Apr; 195(1):518-533. doi: 10.1093/plphys/kiae071. [PMID: 38365203]
  • Meng Wang, Jiaxue Li, Tao Li, Shaoling Kang, Senrong Jiang, Jiaquan Huang, Hua Tang. Light Supplementation in Pitaya Orchards Induces Pitaya Flowering in Winter by Promoting Phytohormone Biosynthesis. International journal of molecular sciences. 2024 Apr; 25(9):. doi: 10.3390/ijms25094794. [PMID: 38732009]
  • Wenting Chai, Bohui Yang, Shanshan Zhao, Zhiqiang Guo, Lixun Zhu, Jiali Fan, Wei Yang, Weijun Zhao, Yanping Hao, Jinhui Lü, Wenxian Sun, Chunlai Zhang. [Characterization of sequences, expression profiling, and natural allelic variation analysis of the MYC gene family in sorghum (Sorghum bicolor)]. Sheng wu gong cheng xue bao = Chinese journal of biotechnology. 2024 Apr; 40(4):1170-1194. doi: 10.13345/j.cjb.230641. [PMID: 38658156]
  • Fan Yan, Junchi Ma, Manjiang Peng, Congfang Xi, Sheng Chang, Ying Yang, Suohui Tian, Bo Zhou, Tao Liu. Lactic acid induced defense responses in tobacco against Phytophthora nicotianae. Scientific reports. 2024 04; 14(1):9338. doi: 10.1038/s41598-024-60037-2. [PMID: 38654120]
  • Lijun Liu, Yuhan Zhang, Chen Tang, Jine Wu, Jingye Fu, Qiang Wang. Genome-wide identification of ZmMYC2 binding sites and target genes in maize. BMC genomics. 2024 Apr; 25(1):397. doi: 10.1186/s12864-024-10297-z. [PMID: 38654166]
  • Yumeng Zhang, Xiaobei Liu, Yu Sun, Yong Liu, Yong Zhang, Tianbo Ding, Julian Chen. Salivary Protein Cyclin-Dependent Kinase-like from Grain Aphid Sitobion avenae Suppresses Wheat Defense Response and Enhances Aphid Adaptation. International journal of molecular sciences. 2024 Apr; 25(9):. doi: 10.3390/ijms25094579. [PMID: 38731798]
  • Tingliang Xu, Xiaowen Zheng, Yi Yang, Shumin Yang, Xingwan Yi, Chao Yu, Le Luo, Jia Wang, Tangren Cheng, Qixiang Zhang, Huitang Pan. Indole-3 acetic acid negatively regulates rose black spot disease resistance through antagonizing the salicylic acid signaling pathway via jasmonic acid. Planta. 2024 Apr; 259(6):129. doi: 10.1007/s00425-024-04406-1. [PMID: 38639804]
  • Mingyue Lu, Boyang Fu, Xiao Meng, Tiantian Jia, Xiaoyue Lu, Chaosha Yang, Ke Li, Pengcheng Yin, Yongfeng Guo, Wei Li, Jina Chi, Geng Wang, Chunjiang Zhou. Transcription factors NtNAC028 and NtNAC080 form heterodimers to regulate jasmonic acid biosynthesis during leaf senescence in Nicotiana tabacum. Journal of experimental botany. 2024 Apr; 75(8):2351-2371. doi: 10.1093/jxb/erae006. [PMID: 38205848]
  • Hong Gao, Jia Ma, Yuxin Zhao, Chuanzhong Zhang, Ming Zhao, Shengfu He, Yan Sun, Xin Fang, Xiaoyu Chen, Kexin Ma, Yanjie Pang, Yachang Gu, Yaqun Dongye, Junjiang Wu, Pengfei Xu, Shuzhen Zhang. The MYB Transcription Factor GmMYB78 Negatively Regulates Phytophthora sojae Resistance in Soybean. International journal of molecular sciences. 2024 Apr; 25(8):. doi: 10.3390/ijms25084247. [PMID: 38673832]
  • Yu Kong, Xianbin Hou, Zhenglu Liu, Yufeng Li. Cold-stress induced metabolomic and transcriptomic changes in leaves of three mango varieties with different cold tolerance. BMC plant biology. 2024 Apr; 24(1):266. doi: 10.1186/s12870-024-04983-z. [PMID: 38600447]
  • Ludan Cao, Guo Wang, Xiuxu Ye, Fang Li, Shujun Wang, Huanling Li, Peng Wang, Jiabao Wang. Physiological, Metabolic, and Transcriptomic Analyses Reveal Mechanisms of Proliferation and Somatic Embryogenesis of Litchi (Litchi chinensis Sonn.) Embryogenic Callus Promoted by D-Arginine Treatment. International journal of molecular sciences. 2024 Apr; 25(7):. doi: 10.3390/ijms25073965. [PMID: 38612774]
  • Sabina A Bajda, Nicky Wybouw, Việt Hà Nguyễn, Patrick De Clercq, Thomas Van Leeuwen. Adaptation of an arthropod predator to a challenging environment is associated with a loss of a genome-wide plastic transcriptional response. Pest management science. 2024 Apr; 80(4):2021-2031. doi: 10.1002/ps.7936. [PMID: 38110295]
  • Shaofang Wu, Chaoyi Hu, Changan Zhu, Yanfen Fan, Jie Zhou, Xiaojia Xia, Kai Shi, Yanhong Zhou, Christine H Foyer, Jingquan Yu. The MYC2-PUB22-JAZ4 module plays a crucial role in jasmonate signaling in tomato. Molecular plant. 2024 Apr; 17(4):598-613. doi: 10.1016/j.molp.2024.02.006. [PMID: 38341757]
  • Tianxia Yang, Lei Deng, Qinyang Wang, Chuanlong Sun, Muhammad Ali, Fangming Wu, Huawei Zhai, Qian Xu, Peiyong Xin, Shujing Cheng, Jinfang Chu, Tingting Huang, Chang-Bao Li, Chuanyou Li. Tomato CYP94C1 inactivates bioactive JA-Ile to attenuate jasmonate-mediated defense during fruit ripening. Molecular plant. 2024 Apr; 17(4):509-512. doi: 10.1016/j.molp.2024.02.004. [PMID: 38327053]
  • José Eduardo Marqués-Gálvez, Gaurav Pandharikar, Veronica Basso, Annegret Kohler, Nathalie D Lackus, Kerrie Barry, Keykhosrow Keymanesh, Jenifer Johnson, Vasanth Singan, Igor V Grigoriev, Rytas Vilgalys, Francis Martin, Claire Veneault-Fourrey. Populus MYC2 orchestrates root transcriptional reprogramming of defence pathway to impair Laccaria bicolor ectomycorrhizal development. The New phytologist. 2024 Apr; 242(2):658-674. doi: 10.1111/nph.19609. [PMID: 38375883]
  • Haoming Zuo, Jiahao Chen, Zhidong Lv, Chenyu Shao, Ziqi Chen, Yuebin Zhou, Chengwen Shen. Tea-Derived Polyphenols Enhance Drought Resistance of Tea Plants (Camellia sinensis) by Alleviating Jasmonate-Isoleucine Pathway and Flavonoid Metabolism Flow. International journal of molecular sciences. 2024 Mar; 25(7):. doi: 10.3390/ijms25073817. [PMID: 38612625]
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  • Swapnil B Kadam, Vitthal T Barvkar. COI1 dependent jasmonic acid signalling positively modulates ROS scavenging system in transgenic hairy root culture of tomato. Plant physiology and biochemistry : PPB. 2023 Nov; 206(?):108229. doi: 10.1016/j.plaphy.2023.108229. [PMID: 38039582]
  • Li-Xian Li, Yue Fang, Dan Li, Zi-Hao Zhu, Ya Zhang, Zi-Yu Tang, Ting Li, Xue-Sen Chen, Shou-Qian Feng. Transcription factors MdMYC2 and MdMYB85 interact with ester aroma synthesis gene MdAAT1 in apple. Plant physiology. 2023 Nov; 193(4):2442-2458. doi: 10.1093/plphys/kiad459. [PMID: 37590971]
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  • Shuangyu Bai, Jiaohui Long, Yuanyuan Cui, Zhaoyi Wang, Caixia Liu, Fenglou Liu, Zhangjun Wang, Qingfeng Li. Regulation of hormone pathways in wheat infested by Blumeria graminis f. sp. tritici. BMC plant biology. 2023 Nov; 23(1):554. doi: 10.1186/s12870-023-04569-1. [PMID: 37940874]
  • Zhongnan Chen, Zhigang Wang, Weihui Xu. Bacillus velezensis WB induces systemic resistance in watermelon against Fusarium wilt. Pest management science. 2023 Nov; ?(?):. doi: 10.1002/ps.7873. [PMID: 37939121]
  • Qingliang Li, Zujun Yin, Wei Tan, Xia Sun, Hui Cao, Deya Wang. The resistance of the jujube (Ziziphus jujuba) to the devastating insect pest Apolygus lucorum (Hemiptera, Insecta) involves the jasmonic acid signaling pathway. Pesticide biochemistry and physiology. 2023 Nov; 196(?):105597. doi: 10.1016/j.pestbp.2023.105597. [PMID: 37945226]