Jasmonate-mediated gibberellin catabolism constrains growth during herbivore attack in rice

Author:

Jin Gaochen1ORCID,Qi Jinfeng2ORCID,Zu Hongyue1ORCID,Liu Shuting1ORCID,Gershenzon Jonathan3ORCID,Lou Yonggen1ORCID,Baldwin Ian T4ORCID,Li Ran1ORCID

Affiliation:

1. State Key Laboratory of Rice Biology, Ministry of Agriculture Key Lab of Molecular Biology of Crop Pathogens and Insects, Key Laboratory of Biology of Crop Pathogens and Insects of Zhejiang Province, Institute of Insect Sciences, Zhejiang University , Hangzhou 310058 , China

2. Department of Economic Plants and Biotechnology, Yunnan Key Laboratory for Wild Plant Resources, Kunming Institute of Botany, Chinese Academy of Sciences , Kunming 650201 , China

3. Department of Biochemistry, Max Planck Institute for Chemical Ecology , Jena 07745 , Germany

4. Department of Molecular Ecology, Max Planck Institute for Chemical Ecology , Jena 07745 , Germany

Abstract

Abstract Plant defense against herbivores is costly and often associated with growth repression. The phytohormone jasmonate (JA) plays a central role in prioritizing defense over growth during herbivore attack, but the underlying mechanisms remain unclear. When brown planthoppers (BPH, Nilaparvata lugens) attack rice (Oryza sativa), growth is dramatically suppressed. BPH infestation also increases inactive gibberellin (GA) levels and transcripts of GA 2-oxidase (GA2ox) genes, 2 (GA2ox3 and GA2ox7) of which encode enzymes that catalyze the conversion of bioactive GAs to inactive GAs in vitro and in vivo. Mutation of these GA2oxs diminishes BPH-elicited growth restriction without affecting BPH resistance. Phytohormone profiling and transcriptome analyses revealed that GA2ox-mediated GA catabolism was enhanced by JA signaling. The transcript levels of GA2ox3 and GA2ox7 were significantly attenuated under BPH attack in JA biosynthesis (allene oxide cyclase [aoc]) or signaling-deficient (myc2) mutants. In contrast, GA2ox3 and GA2ox7 expression was increased in MYC2 overexpression lines. MYC2 directly binds to the G-boxes in the promoters of both GA2ox genes to regulate their expression. We conclude that JA signaling simultaneously activates defense responses and GA catabolism to rapidly optimize resource allocation in attacked plants and provides a mechanism for phytohormone crosstalk.

Funder

National Key Research and Development Program of China

Max Planck Partner Group Program

Hundred-Talent Program of Zhejiang University

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

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