WAV E3 ubiquitin ligases mediate degradation of IAA32/34 in the TMK1-mediated auxin signaling pathway during apical hook development

Author:

Wang Jun-Li12,Wang Ming13,Zhang Li14,Li You-Xia1,Li Jing-Jing1,Li Yu-Yang12,Pu Zuo-Xian12,Li Dan-Yang12,Liu Xing-Nan12,Guo Wang12,Di Dong-Wei15ORCID,Li Xiao-Feng12ORCID,Guo Guang-Qin12ORCID,Wu Lei12ORCID

Affiliation:

1. Ministry of Education Key Laboratory of Cell Activities and Stress Adaptations, School of Life Sciences, Lanzhou University, Lanzhou 730000, People’s Republic of China

2. Gansu Province Key Laboratory of Gene Editing for Breeding, School of Life Sciences, Lanzhou University, Lanzhou 730000, People’s Republic of China

3. Department of Plant Pathology, Nanjing Agricultural University, Nanjing 210008, People’s Republic of China

4. Basic Forestry and Proteomics Research Center, College of Life Sciences, Fujian Agriculture and Forestry University, Fuzhou 350002, People’s Republic of China

5. State Key Laboratory of Soil and Sustainable Agriculture, Institute of Soil Science, Chinese Academy of Sciences, Nanjing 210008, People’s Republic of China

Abstract

Auxin regulates plant growth and development through downstream signaling pathways, including the best-known SCF TIR1/AFB -Aux/IAA-ARF pathway and several other less characterized “noncanonical” pathways. Recently, one SCF TIR1/AFB -independent noncanonical pathway, mediated by Transmembrane Kinase 1 (TMK1), was discovered through the analyses of its functions in Arabidopsis apical hook development. Asymmetric accumulation of auxin on the concave side of the apical hook triggers DAR1-catalyzed release of the C-terminal of TMK1, which migrates into the nucleus, where it phosphorylates and stabilizes IAA32/34 to inhibit cell elongation, which is essential for full apical hook formation. However, the molecular factors mediating IAA32/34 degradation have not been identified. Here, we show that proteins in the CYTOKININ INDUCED ROOT WAVING 1 (CKRW1)/WAVY GROWTH 3 (WAV3) subfamily act as E3 ubiquitin ligases to target IAA32/34 for ubiquitination and degradation, which is inhibited by TMK1c-mediated phosphorylation. This antagonistic interaction between TMK1c and CKRW1/WAV3 subfamily E3 ubiquitin ligases regulates IAA32/34 levels to control differential cell elongation along opposite sides of the apical hook.

Funder

MOST | National Natural Science Foundation of China

甘肃省科学技术厅 | Natural Science Foundation of Gansu Province

Central University Basic Research Fund of China

Publisher

Proceedings of the National Academy of Sciences

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