The Arabidopsis cryptochrome 2 I404F mutant is hypersensitive and shows flavin reduction even in the absence of light

• Published in: Planta Vol. 251; no. 1; p. 33
• Main Authors: Araguirang, Galileo Estopare, Niemann, Nils, Kiontke, Stephan, Eckel, Maike, Dionisio-Sese, Maribel L., Batschauer, Alfred
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.01.2020; Springer Nature B.V
• Subjects: Agriculture; Arabidopsis; Arabidopsis - genetics; Arabidopsis - metabolism; Arabidopsis Proteins - chemistry; Arabidopsis Proteins - genetics; Arabidopsis Proteins - metabolism; Arabidopsis Proteins - radiation effects; Biomedical and Life Sciences; Chromophores; Cryptochromes - chemistry; Cryptochromes - genetics; Cryptochromes - metabolism; Cryptochromes - radiation effects; Ecology; Flavin; Flavins - metabolism; Forestry; Hyperactivity; Hypersensitivity; Life Sciences; Light; Models, Molecular; Mutagenesis, Site-Directed; Mutation; Original Article; Phenotype; Photoreceptors; Plant Sciences; Protein Conformation; Proteins; Reduction; Signal Transduction; Transcription Factors - genetics; Cryptochrome photocycle; Structural changes; Plant biochemistry; ATP-binding; Photobiology; Photoreceptor
• ISSN: 0032-0935; 1432-2048
• DOI: 10.1007/s00425-019-03323-y

Main conclusion The cryptochrome photoreceptor mutant cry2 I404F exhibits hyperactivity in the dark, hypersensitivity in different light conditions, and in contrast to the wild-type protein, its flavin chromophore is reducible even in the absence of light. Plant cryptochromes (cry) are blue-light photoreceptors involved in multiple signaling pathways and various photomorphogenic responses. One biologically hyperactive mutant of a plant cryptochrome that was previously characterized is Arabidopsis cry1 L407F (Exner et al. in Plant Physiol 154:1633–1645, 2010). Protein sequence alignments of different cryptochromes revealed that L407 in cry1 corresponds to I404 in cry2. Point mutation of Ile to Phe in cry2 in this position created a novel mutant. The present study provided a baseline data on the elucidation of the properties of cry2 I404F. This mutant was still able to bind ATP-triggering conformational changes, as confirmed by partial tryptic digestion and thermo-FAD assays. Surprisingly, the FAD cofactor of cry2 I404F was reduced by the addition of reductant even in the absence of light. In vivo , cry2 I404F exhibited a cop phenotype in the dark and hypersensitivity to various light conditions compared to cry2 wild type. Overall, these data suggest that the hypersensitivity to red and blue light and hyperactivity of this novel mutant in the dark can be mostly accounted to structural alterations brought forth by the Ile to Phe mutation at position 404 that allows reduction of the flavin chromophore even in the absence of light.