4.7 Article

A low CO2-responsive mutant of Setaria viridis reveals that reduced carbonic anhydrase limits C4 photosynthesis

期刊

JOURNAL OF EXPERIMENTAL BOTANY
卷 72, 期 8, 页码 3122-3136

出版社

OXFORD UNIV PRESS
DOI: 10.1093/jxb/erab039

关键词

Carbonic anhydrase; C-4 photosynthesis; C-4 rice; forward genetics; mutant screen; Setaria viridis

资金

  1. International Rice Research Institute
  2. Bill and Melinda Gates Foundation [OPPGD1394]
  3. Department for International Development (DFID) UK
  4. ARC Centre of Excellence in Translational Photosynthesis in Australia [CE140100015]
  5. DBT-India's Ramalingaswamy Re-Entry fellowship
  6. Bill and Melinda Gates Foundation [OPPGD1394] Funding Source: Bill and Melinda Gates Foundation

向作者/读者索取更多资源

The study identified a low CO2-responsive mutant Icr1 with a mutation in the beta-carbonic anhydrase (CA) gene, leading to reduced growth and photosynthesis. The mutated gene caused a decrease in CA protein activity and abundance, restricting the supply of bicarbonate to PEPC and ultimately limiting C-4 photosynthesis and growth. These findings highlight the importance of CA in the C-4 photosynthesis pathway and provide insights into potential targets for improving C-4 biochemical pathways in crops like rice.
In C-4 species, beta-carbonic anhydrase (CA), localized to the cytosol of the mesophyll cells, accelerates the interconversion of CO2 to HCO3-, the substrate used by phosphoenolpyruvate carboxylase (PEPC) in the first step of C-4 photosynthesis. Here we describe the identification and characterization of low CO2-responsive mutant 1 (Icr1) isolated from an N-nitroso-N-methylurea- (NMU) treated Setaria viridis mutant population. Forward genetic investigation revealed that the mutated gene Sevir5G247800 of Icr1 possessed a single nucleotide transition from cytosine to thymine in a beta-CA gene causing an amino acid change from leucine to phenylalanine. This resulted in severe reduction in growth and photosynthesis in the mutant. Both the CO2 compensation point and carbon isotope discrimination values of the mutant were significantly increased. Growth of the mutants was stunted when grown under ambient pCO(2) but recovered at elevated pCO(2). Further bioinformatics analyses revealed that the mutation has led to functional changes in one of the conserved residues of the protein, situated near the catalytic site. CA transcript accumulation in the mutant was 80% lower, CA protein accumulation 30% lower, and CA activity similar to 98% lower compared with the wild type. Changes in the abundance of other primary C-4 pathway enzymes were observed; accumulation of PEPC protein was significantly increased and accumulation of malate dehydrogenase and malic enzyme decreased. The reduction of CA protein activity and abundance in Icr1 restricts the supply of bicarbonate to PEPC, limiting C-4 photosynthesis and growth. This study establishes Sevir.5G247800 as the major CA allele in Setaria for C-4 photosynthesis and provides important insights into the function of CA in C-4 photosynthesis that would be required to generate a rice plant with a functional C-4 biochemical pathway.

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