Silencing of OsGRXS17 in rice improves drought stress tolerance by modulating ROS accumulation and stomatal closure

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作者
Ying Hu
Qingyu Wu
Zhao Peng
Stuart A. Sprague
Wei Wang
Jungeun Park
Eduard Akhunov
Krishna S. V. Jagadish
Paul A. Nakata
Ninghui Cheng
Kendal D. Hirschi
Frank F. White
Sunghun Park
机构
[1] Department of Horticulture and Natural Resources,
[2] Kansas State University,undefined
[3] Department of Plant Pathology,undefined
[4] Kansas State University,undefined
[5] Department of Agronomy,undefined
[6] Kansas State University,undefined
[7] United States Department of Agriculture/Agricultural Research Service,undefined
[8] Children’s Nutrition Research Center,undefined
[9] Department of Pediatrics,undefined
[10] Baylor College of Medicine,undefined
[11] Department of Plant Pathology,undefined
[12] Kansas State University,undefined
[13] Cold Spring Harbor Laboratory,undefined
[14] Department of Plant Pathology,undefined
[15] University of Florida,undefined
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摘要
Glutaredoxins (GRXs) modulate redox-dependent signaling pathways and have emerged as key mediators in plant responses to environmental stimuli. Here we report that RNAi-mediated suppression of Oryza sativa GRXS17 (OsGRXS17) improved drought tolerance in rice. Gene expression studies showed that OsGRXS17 was present throughout the plant and that transcript abundance increased in response to drought stress and abscisic acid (ABA) treatment. Localization studies, utilizing GFP-OsGRXS17 fusion proteins, indicated that OsGRXS17 resides in both the cytoplasm and the nuclear envelope. Under drought stress conditions, rice plants with reduced OsGRXS17 expression showed lower rates of water loss and stomatal conductance, higher relative water content, and enhanced survival compared to wild-type controls. Further characterization of the OsGRXS17 down-regulated plants revealed an elevation in H2O2 production within the guard cells, increased sensitivity to ABA, and a reduction in stomatal apertures. The findings demonstrate a critical link between OsGRXS17, the modulation of guard cell H2O2 concentrations, and stomatal closure, expanding our understanding of the mechanisms governing plant responses to drought.
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