GRAS-domain transcription factor PAT1 regulates jasmonic acid biosynthesis in grape cold stress response

Author:

Wang Zemin12ORCID,Wong Darren Chern Jan3,Wang Yi12ORCID,Xu Guangzhao12,Ren Chong1ORCID,Liu Yanfei12,Kuang Yangfu12ORCID,Fan Peige14,Li Shaohua1,Xin Haiping56,Liang Zhenchang1ORCID

Affiliation:

1. Beijing Key Laboratory of Grape Science and Enology, and CAS Key Laboratory of Plant Resources, Institute of Botany, Innovation Academy for Seed Design, the Chinese Academy of Science, Beijing 100093, China

2. University of Chinese Academy of Sciences, Beijing 10049, China

3. Department of Ecology and Evolution, Research School of Biology, Australian National University, Acton, ACT 2601, Australia

4. China Wine Industry Technology Institute, Yinchuan 750021, China

5. Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, Wuhan Botanical Garden, Chinese Academy of Sciences, Wuhan 430074, China

6. Center of Economic Botany, Core Botanical Gardens, Chinese academy of Sciences, Wuhan 430074, China

Abstract

Abstract Cultivated grapevine (Vitis) is a highly valued horticultural crop, and cold stress affects its growth and productivity. Wild Amur grape (Vitis amurensis) PAT1 (Phytochrome A signal transduction 1, VaPAT1) is induced by low temperature, and ectopic expression of VaPAT1 enhances cold tolerance in Arabidopsis (Arabidopsis thaliana). However, little is known about the molecular mechanism of VaPAT1 during the cold stress response in grapevine. Here, we confirmed the overexpression of VaPAT1 in transformed grape calli enhanced cold tolerance. Yeast two-hybrid and bimolecular fluorescence complementation assays highlighted an interaction between VaPAT1 with INDETERMINATE-DOMAIN 3 (VaIDD3). A role of VaIDD3 in cold tolerance was also indicated. Transcriptome analysis revealed VaPAT1 and VaIDD3 overexpression and cold treatment coordinately modulate the expression of stress-related genes including lipoxygenase 3 (LOX3), a gene encoding a key jasmonate biosynthesis enzyme. Co-expression network analysis indicated LOX3 might be a downstream target of VaPAT1. Both electrophoretic mobility shift and dual luciferase reporter assays showed the VaPAT1-IDD3 complex binds to the IDD-box (AGACAAA) in the VaLOX3 promoter to activate its expression. Overexpression of both VaPAT1 and VaIDD3 increased the transcription of VaLOX3 and JA levels in transgenic grape calli. Conversely, VaPAT1-SRDX (dominant repression) and CRISPR/Cas9-mediated mutagenesis of PAT1-ED causing the loss of the C-terminus in grape calli dramatically prohibited the accumulation of VaLOX3 and JA levels during cold treatment. Together, these findings point to a pivotal role of VaPAT1 in the cold stress response in grape by regulating JA biosynthesis.

Funder

National Key Research and Development Program

National Science Foundation of China

Publisher

Oxford University Press (OUP)

Subject

Plant Science,Genetics,Physiology

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