The chemical compound 'Heatin' stimulates hypocotyl elongation and interferes with the Arabidopsis NIT1-subfamily of nitrilases
Woude, Lennard van der; Piotrowski, Markus; Klaasse, Gruson; Paulus, Judith K; Krahn, Daniel; Ninck, Sabrina; Kaschani, Farnusch; Kaiser, Markus; Novák, Ondřej; Ljung, Karin; Bulder, Suzanne; van Verk, Marcel; Snoek, Basten L; Fiers, Martijn; Martin, Nathaniel I; van der Hoorn, Renier A L; Robert, Stéphanie; Smeekens, Sjef; van Zanten, Martijn
(2021) Plant Journal, volume 106, issue 6, pp. 1523 - 1540
(Article)
Abstract
Temperature passively affects biological processes involved in plant growth. Therefore, it is challenging to study the dedicated temperature signalling pathways that orchestrate thermomorphogenesis, a suite of elongation growth-based adaptations that enhance leaf-cooling capacity. We screened a chemical library for compounds that restored hypocotyl elongation in the pif4-2–deficient mutant background at
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warm temperature conditions in Arabidopsis thaliana to identify modulators of thermomorphogenesis. The small aromatic compound ‘Heatin’, containing 1-iminomethyl-2-naphthol as a pharmacophore, was selected as an enhancer of elongation growth. We show that ARABIDOPSIS ALDEHYDE OXIDASES redundantly contribute to Heatin-mediated hypocotyl elongation. Following a chemical proteomics approach, the members of the NITRILASE1-subfamily of auxin biosynthesis enzymes were identified among the molecular targets of Heatin. Our data reveal that nitrilases are involved in promotion of hypocotyl elongation in response to high temperature and Heatin-mediated hypocotyl elongation requires the NITRILASE1-subfamily members, NIT1 and NIT2. Heatin inhibits NIT1-subfamily enzymatic activity in vitro and the application of Heatin accordingly results in the accumulation of NIT1-subfamily substrate indole-3-acetonitrile in vivo. However, levels of the NIT1-subfamily product, bioactive auxin (indole-3-acetic acid), were also significantly increased. It is likely that the stimulation of hypocotyl elongation by Heatin might be independent of its observed interaction with NITRILASE1-subfamily members. However, nitrilases may contribute to the Heatin response by stimulating indole-3-acetic acid biosynthesis in an indirect way. Heatin and its functional analogues present novel chemical entities for studying auxin biology.
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Keywords: 1-iminomethyl-2-naphthol, Arabidopsis, Heatin, IAN, NIT1-subfamily, PIF4, aldehyde oxidase, chemical genetics, indole-3-acetonitrile, nitrilases, thermomorphogenesis, Genetics, Plant Science, Cell Biology
ISSN: 0960-7412
Publisher: Blackwell Publishing Ltd
Note: Funding Information: We thank Per Anders Enquist (Chemical Biology Consortium Sweden Umeå), Christa Testerink and Iko Koevoets (Wageningen University) for advice. Kamaleddin Hajmohammadebrahimtehrani, Colin Snoeker, Jan Orsel and Lennert Zorn (Utrecht University) are thanked for technical assistance. This work was supported by Graduateschool Uitgangsmaterialen grant NWO# 831.13.002 to LvdW and MvZ by the Netherlands Organisation for Scientific research (NWO), a Facility access and support grant for chemical genomics projects to LvdW and MvZ from the Laboratories for Chemical Biology (Chemical Biology Consortium Sweden Umeå), Umeå, Sweden, an Erasmus Placement grant to LvdW, an European Research Council (ERC) starting grant No. 258413 to MK, Deutsche Forschungsgemeinschaft (DFG) grant INST 20876/127‐1 FUGG to MK and ERC consolidator grant 616449 and BBSRC grants BB/R017913/1 and BB/S003193/1 to RH. KL acknowledges support from the Swedish Foundation for Strategic Research (VINNOVA), the Swedish Research Council (VR), the Swedish Metabolomics Centre for the Use of Instrumentation and the Knut and Alice Wallenberg Foundation (KAW). ON was financially supported by the Ministry of Education Youth and Sports of the Czech Republic through the European Regional Development Fund‐Project ‘Plants as a tool for sustainable global development’ (CZ.02.1.01/0.0/0.0/16_019/0000827). Publisher Copyright: © 2021 The Authors. The Plant Journal published by Society for Experimental Biology and John Wiley & Sons Ltd.
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