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Two-component cyclase opsins of green algae are ATP-dependent and light-inhibited guanylyl cyclases

DOI:10.1186/s12915-018-0613-5 期刊:BMC Biology 出版年份:2018 更新时间:2025-09-23 15:22:29
摘要: Background: The green algae Chlamydomonas reinhardtii and Volvox carteri are important models for studying light perception and response, expressing many different photoreceptors. More than 10 opsins were reported in C. reinhardtii, yet only two—the channelrhodopsins—were functionally characterized. Characterization of new opsins would help to understand the green algae photobiology and to develop new tools for optogenetics. Results: Here we report the characterization of a novel opsin family from these green algae: light-inhibited guanylyl cyclases regulated through a two-component-like phosphoryl transfer, called “two-component cyclase opsins” (2c-Cyclops). We prove the existence of such opsins in C. reinhardtii and V. carteri and show that they have cytosolic N- and C-termini, implying an eight-transmembrane helix structure. We also demonstrate that cGMP production is both light-inhibited and ATP-dependent. The cyclase activity of Cr2c-Cyclop1 is kept functional by the ongoing phosphorylation and phosphoryl transfer from the histidine kinase to the response regulator in the dark, proven by mutagenesis. Absorption of a photon inhibits the cyclase activity, most likely by inhibiting the phosphoryl transfer. Overexpression of Vc2c-Cyclop1 protein in V. carteri leads to significantly increased cGMP levels, demonstrating guanylyl cyclase activity of Vc2c-Cyclop1 in vivo. Live cell imaging of YFP-tagged Vc2c-Cyclop1 in V. carteri revealed a development-dependent, layer-like structure at the immediate periphery of the nucleus and intense spots in the cell periphery. Conclusions: Cr2c-Cyclop1 and Vc2c-Cyclop1 are light-inhibited and ATP-dependent guanylyl cyclases with an unusual eight-transmembrane helix structure of the type I opsin domain which we propose to classify as type Ib, in contrast to the 7 TM type Ia opsins. Overexpression of Vc2c-Cyclop1 protein in V. carteri led to a significant increase of cGMP, demonstrating enzyme functionality in the organism of origin. Fluorescent live cell imaging revealed that Vc2c-Cyclop1 is located in the periphery of the nucleus and in confined areas at the cell periphery.
作者: Yuehui Tian,Shiqiang Gao,Eva Laura von der Heyde,Armin Hallmann,Georg Nagel
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Characterization of a novel opsin family from green algae, specifically light-inhibited guanylyl cyclases regulated through a two-component-like phosphoryl transfer, to understand green algae photobiology and develop new tools for optogenetics.

Cr2c-Cyclop1 and Vc2c-Cyclop1 are identified as light-inhibited, ATP-dependent guanylyl cyclases with an eight-transmembrane helix structure, classified as type Ib opsins. They function through a phosphoryl transfer mechanism inhibited by light. Overexpression in V. carteri confirmed in vivo activity, and localization studies revealed specific subcellular structures. These findings advance understanding of algal photobiology and offer potential optogenetic tools for cGMP regulation.

The study is limited to specific green algae species (C. reinhardtii and V. carteri), and the functional role of 2c-Cyclop in its native context is not fully understood due to the presence of multiple photoreceptors and guanylyl cyclases. Expression levels and light inhibition in vivo were less marked compared to in vitro assays. The photocycle turnover time was estimated but not precisely measured.

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