4.8 Article

Photosynthesis-independent production of reactive oxygen species in the rice bundle sheath during high light is mediated by NADPH oxidase

Publisher

NATL ACAD SCIENCES
DOI: 10.1073/pnas.2022702118

Keywords

rice; bundle sheath strands; high light; reactive oxygen species

Funding

  1. China International Postdoctoral Exchange Fellowship
  2. European Research Council [RG80867]
  3. Biotechnology and Biological Sciences Research Council Grant [BBP0031171]
  4. C4 Rice Project Grant from The Bill and Melinda Gates Foundation

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Exposure to high light induces rapid ROS production in bundle-sheath strands compared to mesophyll cells in plants, a response that is independent of CO2 supply or photorespiration but regulated by NADPH oxidase activity.
When exposed to high light, plants produce reactive oxygen species (ROS). In Arabidopsis thaliana, local stress such as excess heat or light initiates a systemic ROS wave in phloem and xylem cells dependent on NADPH oxidase/respiratory burst oxidase homolog (RBOH) proteins. In the case of excess light, although the initial local accumulation of ROS preferentially takes place in bundle-sheath strands, little is known about how this response takes place. Using rice and the ROS probes diaminobenzidine and 2 ',7 '-dichlorodihydro-fluorescein diacetate, we found that, after exposure to high light, ROS were produced more rapidly in bundle-sheath strands than mesophyll cells. This response was not affected either by CO2 supply or photorespiration. Consistent with these findings, deep sequencing of messenger RNA (mRNA) isolated from mesophyll or bundle-sheath strands indicated balanced accumulation of transcripts encoding all major components of the photosynthetic apparatus. However, transcripts encoding several isoforms of the superoxide/H2O2-producing enzyme NADPH oxidase were more abundant in bundle-sheath strands than mesophyll cells. ROS production in bundle-sheath strands was decreased in mutant alleles of the bundle-sheath strand preferential isoform of OsRBOHA and increased when it was over expressed. Despite the plethora of pathways able to generate ROS in response to excess light, NADPH oxidase-mediated accumulation of ROS in the rice bundle-sheath strand was detected in etiolated leaves lacking chlorophyll. We conclude that photosynthesis is not necessary for the local ROS response to high light but is in part mediated by NADPH oxidase activity.

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