Regulation by distinct MYB transcription factors defines the roles of OsCYP86A9 in anther development and root suberin deposition

Author:

Huang Xiaoyan1,Li Yiqi1,Chang Zhenyi1,Yan Wei1,Xu Chunjue23,Zhang Baolei4,He Zhaohuan5,Wang Changjian1,Zheng Minting1,Li Zhiai1,Xia Jixing4ORCID,Li Guoliang5,Tang Xiaoyan123ORCID,Wu Jianxin1ORCID

Affiliation:

1. Guangdong Provincial Key Laboratory of Biotechnology for Plant Development, School of Life Sciences South China Normal University Guangzhou 510631 China

2. Shenzhen Branch, Guangdong Laboratory for Lingnan Modern Agriculture Agricultural Genomics Institute at Shenzhen, Chinese Academy of Agricultural Sciences Shenzhen 518120 China

3. Shenzhen Institute of Molecular Crop Design Shenzhen 518107 China

4. State Key Laboratory for Conservation and Utilization of Subtropical Agro‐bioresources, College of Life Science and Technology Guangxi University Nanning 530004 China

5. Key Laboratory of Plant Nutrition and Fertilizer in South Region, Ministry of Agriculture and Rural Affairs, Guangdong Key Laboratory of Nutrient Cycling and Farmland Conservation Institute of Agricultural Resources and Environment, Guangdong Academy of Agricultural Sciences Guangzhou Guangdong 510640 China

Abstract

SUMMARYCytochrome P450 proteins (CYPs) play critical roles in plant development and adaptation to fluctuating environments. Previous reports have shown that CYP86A proteins are involved in the biosynthesis of suberin and cutin in Arabidopsis. However, the functions of these proteins in rice remain obscure. In this study, a rice mutant with incomplete male sterility was identified. Cytological analyses revealed that this mutant was defective in anther development. Cloning of the mutant gene indicated that the responsible mutation was on OsCYP86A9. OsMYB80 is a core transcription factor in the regulation of rice anther development. The expression of OsCYP86A9 was abolished in the anther of osmyb80 mutant. In vivo and in vitro experiments showed that OsMYB80 binds to the MYB‐binding motifs in OsCYP86A9 promoter region and regulates its expression. Furthermore, the oscyp86a9 mutant exhibited an impaired suberin deposition in the root, and was more susceptible to drought stress. Interestingly, genetic and biochemical analyses revealed that OsCYP86A9 expression was regulated in the root by certain MYB transcription factors other than OsMYB80. Moreover, mutations in the MYB genes that regulate OsCYP86A9 expression in the root did not impair the male fertility of the plant. Taken together, these findings revealed the critical roles of OsCYP86A9 in plant development and proposed that OsCYP86A9 functions in anther development and root suberin formation via two distinct tissue‐specific regulatory pathways.

Funder

Natural Science Foundation of Guangdong Province

Publisher

Wiley

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