A nuclear CobW/WW-domain factor represses the CO <sub>2</sub> -concentrating mechanism in the green alga <i>Chlamydomonas reinhardtii</i>

Microalgae induce a CO<sub>2</sub>-concentrating mechanism (CCM) to maintain photosynthesis when CO<sub>2</sub> is limited. Because this system consumes a substantial portion of photosynthetically generated ATP, its suppression when CO<sub>2</sub> levels rise is critical for energy balance, yet the underlying mechanism remains unclear. Here, we identify a nuclear repressor of the CCM in the green alga <i>Chlamydomonas reinhardtii</i>. A pull-down screen for interacting partners of the master activator CCM1/CIA5 revealed an uncharacterized protein that tightly associates with CCM1. This protein, CCM1-binding protein 1 (CBP1), combines a CobW/CobW_C GTP-binding metallochaperone module with a WW-domain characteristic of protein-protein interactions. CBP1 colocalizes and interacts with CCM1 in the nucleus regardless of CO<sub>2</sub> conditions. Disruption of CBP1 does not affect growth or CCM induction under CO<sub>2</sub> limitation but derepresses 27 of 41 CCM1-dependent low-CO<sub>2</sub> inducible genes under high-CO<sub>2</sub> conditions. These include the periplasmic and intracellular carbonic anhydrases (CAH1 and LCIB) and inorganic carbon transporters/channels (LCIA, LCI1, BST1, and BST3). Consistently, <i>cbp1</i> mutants accumulate CAH1 and LCIB proteins and exhibit 40% higher inorganic carbon affinity under high-CO<sub>2</sub> conditions; this phenotype is rescued by CBP1 complementation or by acetazolamide treatment. Crucially, <i>cbp1</i> mutants exhibit significant growth delays under high-CO<sub>2</sub> conditions, especially when light is limiting, providing direct evidence that CBP1-mediated repression is essential for energy conservation. Thus, CBP1 prevents unnecessary CCM activity when CO<sub>2</sub> is abundant, acting upstream of both transporter/channel and carbonic anhydrase modules. Our findings suggest a regulatory mechanism potentially linking zinc-dependent protein chemistry to CCM gene repression, providing insights into energy-efficient CO<sub>2</sub> sensing in aquatic photosynthetic organisms.

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Proceedings of the National Academy of Sciences
Published
2026-02-04
DOI
https://doi.org/10.1073/pnas.2518136123
Primary Topic
Photosynthetic Processes and Mechanisms
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article
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article

A nuclear CobW/WW-domain factor represses the CO 2 -concentrating mechanism in the green alga Chlamydomonas reinhardtii

Ayumi Yamagami, Daisuke Shimamura, Hideya Fukuzawa, Yuichiro Takahashi et al.
Proceedings of the National Academy of Sciences
Photosynthetic Processes and Mechanisms
article

A nuclear CobW/WW-domain factor represses the CO 2 -concentrating mechanism in the green alga Chlamydomonas reinhardtii

Ayumi Yamagami, Daisuke Shimamura, Hideya Fukuzawa, Yuichiro Takahashi, Takashi Yamano, Ozawa Shin-ichiro, Takeshi Nakano, H Nakano, Tomonao Matsushita, Junko Yasuda, Ryutaro Tokutsu, Yosuke Yamahara
article en

Abstract

Microalgae induce a CO<sub>2</sub>-concentrating mechanism (CCM) to maintain photosynthesis when CO<sub>2</sub> is limited. Because this system consumes a substantial portion of photosynthetically generated ATP, its suppression when CO<sub>2</sub> levels rise is critical for energy balance, yet the underlying mechanism remains unclear. Here, we identify a nuclear repressor of the CCM in the green alga <i>Chlamydomonas reinhardtii</i>. A pull-down screen for interacting partners of the master activator CCM1/CIA5 revealed an uncharacterized protein that tightly associates with CCM1. This protein, CCM1-binding protein 1 (CBP1), combines a CobW/CobW_C GTP-binding metallochaperone module with a WW-domain characteristic of protein-protein interactions. CBP1 colocalizes and interacts with CCM1 in the nucleus regardless of CO<sub>2</sub> conditions. Disruption of CBP1 does not affect growth or CCM induction under CO<sub>2</sub> limitation but derepresses 27 of 41 CCM1-dependent low-CO<sub>2</sub> inducible genes under high-CO<sub>2</sub> conditions. These include the periplasmic and intracellular carbonic anhydrases (CAH1 and LCIB) and inorganic carbon transporters/channels (LCIA, LCI1, BST1, and BST3). Consistently, <i>cbp1</i> mutants accumulate CAH1 and LCIB proteins and exhibit 40% higher inorganic carbon affinity under high-CO<sub>2</sub> conditions; this phenotype is rescued by CBP1 complementation or by acetazolamide treatment. Crucially, <i>cbp1</i> mutants exhibit significant growth delays under high-CO<sub>2</sub> conditions, especially when light is limiting, providing direct evidence that CBP1-mediated repression is essential for energy conservation. Thus, CBP1 prevents unnecessary CCM activity when CO<sub>2</sub> is abundant, acting upstream of both transporter/channel and carbonic anhydrase modules. Our findings suggest a regulatory mechanism potentially linking zinc-dependent protein chemistry to CCM gene repression, providing insights into energy-efficient CO<sub>2</sub> sensing in aquatic photosynthetic organisms.

Proceedings of the National Academy of SciencesVol. 123(6)
Okayama University (JP), Kyoto Women's University (JP), Kyoto University (JP), RIKEN Center for Sustainable Resource Science (JP), Living Systems (United States) (US), Kitasato University (JP)
Affordable and clean energy
Openalex Percentile: Top 68%
Photosynthetic Processes and Mechanisms
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