Identification and structure-guided development of triazole urea-based selective antagonists of Arabidopsis karrikin signaling

The smoke-derived butenolides, karrikins (KARs), regulate many aspects of plant growth and development. However, KARs and a plant hormone, strigolactones (SLs), have high resemblance in signal perception and transduction, making it hard to delineate KARs response due to the shortage of chemical-gene...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Nature communications 2025-01, Vol.16 (1), p.104-13, Article 104
Hauptverfasser: Wang, Jianwen, Takahashi, Ikuo, Kikuzato, Ko, Sakai, Toshihiko, Zhu, Zhangliang, Jiang, Kai, Nakamura, Hidemitsu, Nakano, Takeshi, Tanokura, Masaru, Miyakawa, Takuya, Asami, Tadao
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:The smoke-derived butenolides, karrikins (KARs), regulate many aspects of plant growth and development. However, KARs and a plant hormone, strigolactones (SLs), have high resemblance in signal perception and transduction, making it hard to delineate KARs response due to the shortage of chemical-genetic tools. Here, we identify a triazole urea KK181N1 as an inhibitor of the KARs receptor KAI2. KK181N1 selectively depress the KAR-induced phenotypes in Arabidopsis . We further elucidate the antagonistic, KAI2 binding mechanism of KK181N1, showing that KK181N1 binds to the catalytic pockets of KAI2 in a non-covalent binding manner. Our experiments also demonstrate the binding affinity of triazole urea compounds are regulated by the structured water molecule networks. By fine-tuning this network, we successfully develop a more potent derivative of KK181N1. We anticipate that these chemicals will be applicable to the elucidation of KARs biology, especially for discriminating the molecular and physiological aspects of KARs and SL signaling. Here, the triazole urea compound KK181N1 is identified as a Karrikin signaling-specific antagonist with a non-covalent binding mode, contrasting the covalent binding of the D14 antagonist KK094. This chemical tool holds potential in discriminating the KARs and SL signaling.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-024-54801-1