» Articles » PMID: 25636203

Gene Knockout of Glutathione Reductase 3 Results in Increased Sensitivity to Salt Stress in Rice

Overview
Journal Plant Mol Biol
Date 2015 Feb 1
PMID 25636203
Citations 31
Authors
Affiliations
Soon will be listed here.
Abstract

Glutathione reductase (GR) is one of important antioxidant enzymes in plants. This enzyme catalyzes the reduction of glutathione disulfide (GSSG) to reduced glutathione (GSH) with the accompanying oxidation of NADPH. Previously, we showed that salt-stress-responsive GR3 is a functional protein localized in chloroplasts and mitochondria in rice. To learn more about the role of GR3 in salt-stress tolerance, we investigated the response to 100 mM NaCl treatment in wild-type rice (WT); GR3 knockout mutant of rice (gr3); and the functional gr3-complementation line (C1). Rice GR3 was primarily expressed in roots at the seedling stage and ubiquitously expressed in all tissues except the sheath at heading stage. GR3 promoter-GUS was expressed in the vascular cylinder and cortex of root tissues in rice seedlings, vascular tissue of nodes, embryo and aleurone layer of seeds, and young flowers. Under both normal and salt-stress conditions, total GR activity was decreased by 20 % in gr3. Oxidative stress, indicated by malondialdehyde content, was greater in gr3 than the WT under salt stress. As compared with the WT, gr3 was sensitive to salt and methyl viologen; it showed inhibited growth, decreased maximal efficiency of photosystem II, decreased GSH and GSSG contents, and the ratio of GSH to GSSG. Conversely, the gr3-complementation line C1 rescued the tolerance to methyl viologen and salinity and recovered the growth and physiological damage caused by salinity. These results reveal that GR3 plays an important role in salt stress tolerance by regulating the GSH redox state in rice.

Citing Articles

Tetraspanin 5 orchestrates resilience to salt stress through the regulation of ion and reactive oxygen species homeostasis in rice.

Mani B, Kaur I, Dhingra Y, Saxena V, Krishna G, Kumar R Plant Biotechnol J. 2024; 23(1):51-71.

PMID: 39356169 PMC: 11672754. DOI: 10.1111/pbi.14476.


Regulation of nitro-oxidative homeostasis: an effective approach to enhance salinity tolerance in plants.

Basu S, Kumar G Plant Cell Rep. 2024; 43(8):193.

PMID: 39008125 DOI: 10.1007/s00299-024-03275-y.


Overexpression of Abscisic Acid Biosynthesis Gene Enhances Survival Rate and Tolerance to Alkaline Stress in Rice Seedlings.

Feng Z, Xu Y, Xie Z, Yang Y, Lu G, Jin Y Plants (Basel). 2024; 13(12).

PMID: 38931145 PMC: 11207436. DOI: 10.3390/plants13121713.


Sensitivity and responses of chloroplasts to salt stress in plants.

Wang X, Chen Z, Sui N Front Plant Sci. 2024; 15:1374086.

PMID: 38693929 PMC: 11061501. DOI: 10.3389/fpls.2024.1374086.


QTLs and Genes for Salt Stress Tolerance: A Journey from Seed to Seed Continued.

Tiwari K, Tiwari S, Kumar N, Sinha S, Krishnamurthy S, Singh R Plants (Basel). 2024; 13(8).

PMID: 38674508 PMC: 11054697. DOI: 10.3390/plants13081099.


References
1.
Edwards E, Rawsthorne S, Mullineaux P . Subcellular distribution of multiple forms of glutathione reductase in leaves of pea (Pisum sativum L.). Planta. 2013; 180(2):278-84. DOI: 10.1007/BF00194008. View

2.
Munns R, Tester M . Mechanisms of salinity tolerance. Annu Rev Plant Biol. 2008; 59:651-81. DOI: 10.1146/annurev.arplant.59.032607.092911. View

3.
Asada K . THE WATER-WATER CYCLE IN CHLOROPLASTS: Scavenging of Active Oxygens and Dissipation of Excess Photons. Annu Rev Plant Physiol Plant Mol Biol. 2004; 50:601-639. DOI: 10.1146/annurev.arplant.50.1.601. View

4.
Sheu J, Yu T, Tong W, Yu S . Carbohydrate starvation stimulates differential expression of rice alpha-amylase genes that is modulated through complicated transcriptional and posttranscriptional processes. J Biol Chem. 1996; 271(43):26998-7004. DOI: 10.1074/jbc.271.43.26998. View

5.
Munns R . Comparative physiology of salt and water stress. Plant Cell Environ. 2002; 25(2):239-250. DOI: 10.1046/j.0016-8025.2001.00808.x. View