Diversity of rhodopsin cyclases in zoospore-forming fungi

• Published in: Proceedings of the National Academy of Sciences - PNAS Vol. 120; no. 44; p. e2310600120
• Main Authors: Broser, Matthias, Busse, Wayne, Spreen, Anika, Reh, Maila, Bernal Sierra, Yinth Andrea, Hwang, Songhwan, Utesch, Tillmann, Sun, Han, Hegemann, Peter
• Format: Journal Article
• Language: English
• Published: United States National Academy of Sciences 31.10.2023
• Subjects: Adaptation; Animals; Biological Sciences; Chimeras; Chromophores; Electromagnetic absorption; Fluorescence; Fungi; Gene duplication; Guanylate Cyclase - genetics; I.R. radiation; Light; Mammalian cells; Mammals; Near infrared radiation; Orientation; Photoreceptor Cells; Photoreceptors; Red shift; Retina; Retinal ganglion cells; Rhodopsin; Rhodopsin - genetics; Spectral sensitivity; enzyme-rhodopsins; fluorescence; fungal-rhodopsins; near infra red light sensing
• ISSN: 0027-8424; 1091-6490
• DOI: 10.1073/pnas.2310600120

Light perception for orientation in zoospore-forming fungi is linked to homo- or heterodimeric rhodopsin-guanylyl cyclases (RGCs). Heterodimeric RGCs, first identified in the chytrid , consist of an unusual near-infrared absorbing highly fluorescent sensitizer neorhodopsin (NeoR) that is paired with a visual light-absorbing rhodopsin responsible for enzyme activation. Here, we present a comprehensive analysis of the distribution of RGC genes in early-branching fungi using currently available genetic data. Among the characterized RGCs, we identified red-sensitive homodimeric RGC variants with maximal light activation close to 600 nm, which allow for red-light control of GTP to cGMP conversion in mammalian cells. Heterodimeric RGC complexes have evolved due to a single gene duplication within the branching of Chytridiales and show a spectral range for maximal light activation between 480 to 600 nm. In contrast, the spectral sensitivity of NeoRs is reaching into the near-infrared range with maximal absorption between 641 and 721 nm, setting the low energy spectral edge of rhodopsins so far. Based on natural NeoR variants and mutational studies, we reevaluated the role of the counterion-triad proposed to cause the extreme redshift. With the help of chimera constructs, we disclose that the cyclase domain is crucial for functioning as homo- or heterodimers, which enables the adaptation of the spectral sensitivity by modular exchange of the photosensor. The extreme spectral plasticity of retinal chromophores in native photoreceptors provides broad perspectives on the achievable spectral adaptation for rhodopsin-based molecular tools ranging from UVB into the near-infrared.