Identification of a gene controlling levels of the copper response regulator 1 transcription factor in <i>Chlamydomonas reinhardtii</i>

Oxygen prevents hydrogen production in Chlamydomonas (Chlamydomonas reinhardtii), in part by inhibiting the transcription of hydrogenase genes. We developed a screen for mutants showing constitutive accumulation of iron hydrogenase 1 (HYDA1) transcripts in normoxia. A reporter gene required for ciliary motility placed under the control of the HYDA1 promoter conferred motility only in hypoxia. By selecting for mutants able to swim even in normoxia, we obtained strains that constitutively express the reporter gene. One identified mutant was affected in a gene encoding an F-box protein 3 (FBXO3) that participates in ubiquitylation and proteasomal degradation pathways in other eukaryotes. Transcriptome profiles revealed that the mutation, termed cehc1-1 (constitutive expression of hydrogenases and copper-responsive genes), triggers the upregulation of genes known to be targets of copper response regulator 1 (CRR1), a transcription factor involved in the nutritional copper signaling pathway and in the hypoxia response pathway. CRR1 was required for upregulating the HYDA1 reporter gene expression in response to hypoxia and for the constitutive expression of the reporter gene in cehc1-1 mutant cells. The CRR1 protein, normally degraded in Cu-supplemented cells, was stabilized in cehc1-1 cells, supporting the conclusion that CEHC1 facilitates CRR1 degradation. Our results describe a previously unknown pathway for CRR1 inhibition and possibly other pathways leading to complex metabolic changes.

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Publication Details

Journal
The Plant Cell
Published
2024-12-23
DOI
https://doi.org/10.1093/plcell/koae300
Citations
2
Primary Topic
Mitochondrial Function and Pathology
Type
article
Field-Weighted Citation Impact
0.47

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article

Identification of a gene controlling levels of the copper response regulator 1 transcription factor in Chlamydomonas reinhardtii

Anne Glaesener, Sean D. Gallaher, Carolyn D. Silflow, Xiaoqing Sun et al.
2 citations
The Plant Cell
Mitochondrial Function and Pathology
0.47
article

Identification of a gene controlling levels of the copper response regulator 1 transcription factor in Chlamydomonas reinhardtii

Anne Glaesener, Sean D. Gallaher, Carolyn D. Silflow, Xiaoqing Sun, Paul A. Lefebvre, Radhika Mehta, Sabeeha Merchant, Daniela Strenkert, M. C. Lavoie
article en
2 citations

Abstract

Oxygen prevents hydrogen production in Chlamydomonas (Chlamydomonas reinhardtii), in part by inhibiting the transcription of hydrogenase genes. We developed a screen for mutants showing constitutive accumulation of iron hydrogenase 1 (HYDA1) transcripts in normoxia. A reporter gene required for ciliary motility placed under the control of the HYDA1 promoter conferred motility only in hypoxia. By selecting for mutants able to swim even in normoxia, we obtained strains that constitutively express the reporter gene. One identified mutant was affected in a gene encoding an F-box protein 3 (FBXO3) that participates in ubiquitylation and proteasomal degradation pathways in other eukaryotes. Transcriptome profiles revealed that the mutation, termed cehc1-1 (constitutive expression of hydrogenases and copper-responsive genes), triggers the upregulation of genes known to be targets of copper response regulator 1 (CRR1), a transcription factor involved in the nutritional copper signaling pathway and in the hypoxia response pathway. CRR1 was required for upregulating the HYDA1 reporter gene expression in response to hypoxia and for the constitutive expression of the reporter gene in cehc1-1 mutant cells. The CRR1 protein, normally degraded in Cu-supplemented cells, was stabilized in cehc1-1 cells, supporting the conclusion that CEHC1 facilitates CRR1 degradation. Our results describe a previously unknown pathway for CRR1 inhibition and possibly other pathways leading to complex metabolic changes.

The Plant CellVol. 37(1)
University of Minnesota (US), Quantitative BioSciences (US), University of California, Berkeley (US)
National Science Foundation, University of Minnesota, Norges Idrettshøgskole, Neurosciences Foundation, National Institutes of Health, Institute on the Environment, University of Minnesota, Genomics Center, University of Minnesota
Zero hunger
Openalex Percentile: Top 33%
Mitochondrial Function and Pathology
0.47
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