A chloroplast sulphate transporter modulates glutathione‐mediated redox cycling to regulate cell division

Author:

Huang Pin‐jui123,Lin Yen‐Ling12,Chen Chun‐Han12,Lin Hsiang‐Yin12ORCID,Fang Su‐Chiung123ORCID

Affiliation:

1. Biotechnology Center in Southern Taiwan Academia Sinica Tainan Taiwan

2. Agricultural Biotechnology Research Center Academia Sinica Taipei Taiwan

3. Institute of Tropical Plant Sciences and Microbiology National Cheng Kung University Tainan Taiwan

Abstract

AbstractGlutathione redox cycling is important for cell cycle regulation, but its mechanisms are not well understood. We previously identified a small‐sized mutant, suppressor of mat3 15‐1 (smt15‐1) that has elevated cellular glutathione. Here, we demonstrated that SMT15 is a chloroplast sulphate transporter. Reducing expression of γ‐GLUTAMYLCYSTEINE SYNTHETASE, encoding the rate‐limiting enzyme required for glutathione biosynthesis, corrected the size defect of smt15‐1 cells. Overexpressing GLUTATHIONE SYNTHETASE (GSH2) recapitulated the small‐size phenotype of smt15‐1 mutant, confirming the role of glutathione in cell division. Hence, SMT15 may regulate chloroplast sulphate concentration to modulate cellular glutathione levels. In wild‐type cells, glutathione and/or thiol‐containing molecules (GSH/thiol) accumulated in the cytosol at the G1 phase and decreased as cells entered the S/M phase. While the cytosolic GSH/thiol levels in the small‐sized mutants, smt15‐1 and GSH2 overexpressors, mirrored those of wild‐type cells (accumulating during G1 and declining at early S/M phase), GSH/thiol was specifically accumulated in the basal bodies at early S/M phase in the small‐sized mutants. Therefore, we propose that GSH/thiol‐mediated redox signalling in the basal bodies may regulate mitotic division number in Chlamydomonas reinhardtii. Our findings suggest a new mechanism by which glutathione regulates the multiple fission cell cycle in C. reinhardtii.

Publisher

Wiley

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