Brassinosteroids promote etiolated apical structures in darkness by amplifying the ethylene response via the EBF-EIN3/PIF3 circuit

Author:

Wang Jiajun123ORCID,Sun Ning4ORCID,Zheng Lidan23ORCID,Zhang Fangfang23ORCID,Xiang Mengda1ORCID,Chen Haodong23ORCID,Deng Xing Wang235ORCID,Wei Ning1ORCID

Affiliation:

1. School of Life Sciences, Southwest University , Chongqing 400715, China

2. State Key Laboratory of Protein and Plant Gene Research, School of Advanced Agricultural Sciences and Life Sciences, Peking University , Beijing 100871, China

3. Peking-Tsinghua Center for Life Sciences, Academy for Advanced Interdisciplinary Studies, Peking University , Beijing 100871, China

4. Key Laboratory of Growth Regulation and Transformation Research of Zhejiang Province, School of Life Sciences, Westlake University , 18 Shilongshan Road , Hangzhou 310024, China

5. Key Laboratory of Molecular Design for Plant Cell Factory of Guangdong Higher Education Institutes, Institute of Plant and Food Science, School of Life Sciences, Southern University of Science and Technology , Shenzhen 518055, China

Abstract

Abstract Germinated plants grow in darkness until they emerge above the soil. To help the seedling penetrate the soil, most dicot seedlings develop an etiolated apical structure consisting of an apical hook and folded, unexpanded cotyledons atop a rapidly elongating hypocotyl. Brassinosteroids (BRs) are necessary for etiolated apical development, but their precise role and mechanisms remain unclear. Arabidopsis thaliana SMALL AUXIN UP RNA17 (SAUR17) is an apical-organ-specific regulator that promotes production of an apical hook and closed cotyledons. In darkness, ethylene and BRs stimulate SAUR17 expression by transcription factor complexes containing PHYTOCHROME-INTERACTING FACTORs (PIFs), ETHYLENE INSENSITIVE 3 (EIN3), and its homolog EIN3-LIKE 1 (EIL1), and BRASSINAZOLE RESISTANT1 (BZR1). BZR1 requires EIN3 and PIFs for enhanced DNA-binding and transcriptional activation of the SAUR17 promoter; while EIN3, PIF3, and PIF4 stability depends on BR signaling. BZR1 transcriptionally downregulates EIN3-BINDING F-BOX 1 and 2 (EBF1 and EBF2), which encode ubiquitin ligases mediating EIN3 and PIF3 protein degradation. By modulating the EBF-EIN3/PIF protein-stability circuit, BRs induce EIN3 and PIF3 accumulation, which underlies BR-responsive expression of SAUR17 and HOOKLESS1 and ultimately apical hook development. We suggest that in the etiolated development of apical structures, BRs primarily modulate plant sensitivity to darkness and ethylene.

Funder

National Key R&D Program of China

National Natural Science Foundation of China

Chongqing Postdoctoral Innovative Talent Support Program 2020

China Postdoctoral Science Foundation

Peking-Tsinghua Center for Life Sciences

State Key Laboratory of Protein and Plant Gene Research

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

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