A Small-Molecule Screen Identifiesl-Kynurenine as a Competitive Inhibitor of TAA1/TAR Activity in Ethylene-Directed Auxin Biosynthesis and Root Growth inArabidopsis

Author:

He Wenrong1,Brumos Javier2,Li Hongjiang13,Ji Yusi1,Ke Meng4,Gong Xinqi4,Zeng Qinglong1,Li Wenyang1,Zhang Xinyan1,An Fengying1,Wen Xing1,Li Pengpeng1,Chu Jinfang5,Sun Xiaohong5,Yan Cunyu5,Yan Nieng4,Xie De-Yu6,Raikhel Natasha3,Yang Zhenbiao3,Stepanova Anna N.2,Alonso Jose M.2,Guo Hongwei1

Affiliation:

1. State Key Laboratory of Protein and Plant Gene Research, College of Life Sciences, Peking University, Peking-Tsinghua Center for Life Sciences, Beijing 100871, China

2. Department of Genetics, North Carolina State University, Raleigh, North Carolina 27695

3. Center for Plant Cell Biology, Department of Botany and Plant Sciences, University of California, Riverside, California 92507

4. Center for Structural Biology, School of Life Sciences, Tsinghua University, Beijing 100084, China

5. National Center for Plant Gene Research, Institute of Genetics and Developmental Biology, Chinese Academy of Sciences, Beijing 100101, China

6. Department of Plant Biology, North Carolina State University, Raleigh, North Carolina 27695

Abstract

AbstractThe interactions between phytohormones are crucial for plants to adapt to complex environmental changes. One example is the ethylene-regulated local auxin biosynthesis in roots, which partly contributes to ethylene-directed root development and gravitropism. Using a chemical biology approach, we identified a small molecule, l-kynurenine (Kyn), which effectively inhibited ethylene responses in Arabidopsis thaliana root tissues. Kyn application repressed nuclear accumulation of the ETHYLENE INSENSITIVE3 (EIN3) transcription factor. Moreover, Kyn application decreased ethylene-induced auxin biosynthesis in roots, and TRYPTOPHAN AMINOTRANSFERASE OF ARABIDOPSIS1/TRYPTOPHAN AMINOTRANSFERASE RELATEDs (TAA1/TARs), the key enzymes in the indole-3-pyruvic acid pathway of auxin biosynthesis, were identified as the molecular targets of Kyn. Further biochemical and phenotypic analyses revealed that Kyn, being an alternate substrate, competitively inhibits TAA1/TAR activity, and Kyn treatment mimicked the loss of TAA1/TAR functions. Molecular modeling and sequence alignments suggested that Kyn effectively and selectively binds to the substrate pocket of TAA1/TAR proteins but not those of other families of aminotransferases. To elucidate the destabilizing effect of Kyn on EIN3, we further found that auxin enhanced EIN3 nuclear accumulation in an EIN3 BINDING F-BOX PROTEIN1 (EBF1)/EBF2-dependent manner, suggesting the existence of a positive feedback loop between auxin biosynthesis and ethylene signaling. Thus, our study not only reveals a new level of interactions between ethylene and auxin pathways but also offers an efficient method to explore and exploit TAA1/TAR-dependent auxin biosynthesis.

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

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