Qing Wang 1 2, Kjell De Vriese 1 2, Sandrien Desmet 3, Ren Wang 4, Markéta Luklová 4, Qianqian Liu 4, Jacob Pollier 3, Qing Lu 1 2, Sarah Schlag 5, Walter Vetter 5, Alain Goossens 1 2, Eugenia Russinova 1 2, Geert Goeminne 3, Danny Geelen 4, Tom Beeckman 1 2, Steffen Vanneste 1 2 4
- PMID: 39680055
- DOI: 10.1093/jxb/erae481
Abstract
Sterols are produced via complex, multistep biosynthetic pathways involving similar enzymatic conversions in plants, animals and fungi, yielding a variety of sterol metabolites with slightly different chemical properties to exert diverse and specific functions. A tremendously diverse landscape of sterols, and sterol-derived compounds, can be found across the plant kingdom, determining a wide spectrum of functions. Resolving the underlying biosynthetic pathways is thus instrumental to understanding the function and use of these molecules. In only a few plants, sterol biosynthesis has been studied using mutants. In non-model species a pharmacological approach is required. However, this relies on only a few inhibitors. Here, we probed a collection of inhibitors of mammalian cholesterol biosynthesis to identify new inhibitors of plant sterol biosynthesis. We show that imidazole-type fungicides, bifonazole, clotrimazole and econazole inhibit the obtusifoliol 14α-demethylase CYP51 in plants. Moreover, we found that the selective estrogen receptor modulator, clomiphene, inhibits sterol biosynthesis in part by inhibiting the plant-specific cyclopropyl-cycloisomerase CPI1. These results demonstrate that rescreening of inhibitors animal sterol biosynthesis is an easy approach for identifying novel inhibitors of plant sterol biosynthesis. These molecules expand the toolkit for studying and manipulating sterol biosynthesis in the plant kingdom.
Keywords: Arabidopsis; CYP51; Sterol biosynthesis; auxin; cell division; cyclopropyl-cycloisomerase; hypocotyl; inhibitor; root.
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