@article{15003fceec2b4e0094a4beec24b2317c,
title = "Sodium sequestration confers salinity tolerance in an ancestral wild rice",
abstract = "Wild rice Oryza rufipogon, a progenitor of cultivated rice Oryza sativa L., possesses superior salinity tolerance and is a potential donor for breeding salinity tolerance traits in rice. However, a mechanistic basis of salinity tolerance in this donor species has not been established. Here, we examined salinity tolerance from the early vegetative stage to maturity in O. rufipogon in comparison with a salt-susceptible (Koshihikari) and a salt-tolerant (Reiziq) variety of O. sativa. We assessed their phylogeny and agronomical traits, photosynthetic performance, ion contents, as well as gene expression in response to salinity stress. Salt-tolerant O. rufipogon exhibited efficient leaf photosynthesis and less damage to leaf tissues during the course of salinity treatment. In addition, O. rufipogon showed a significantly higher tissue Na+ accumulation that is achieved by vacuolar sequestration compared to the salt tolerant O. sativa indica subspecies. These findings are further supported by the upregulation of genes involved with ion transport and sequestration (e.g. high affinity K+ transporter 1;4 [HKT1;4], Na+/H+ exchanger 1 [NHX1] and vacuolar H+-ATPase c [VHA-c]) in salt-tolerant O. rufipogon as well as by the close phylogenetic relationship of key salt-responsive genes in O. rufipogon to these in salt-tolerant wild rice species such as O. coarctata. Thus, the high accumulation of Na+ in the leaves of O. rufipogon acts as a cheap osmoticum to minimize the high energy cost of osmolyte biosynthesis and excessive reactive oxygen species production. These mechanisms demonstrated that O. rufipogon has important traits that can be used for improving salinity tolerance in cultivated rice.",
keywords = "gene expression, ion transporters, Oryza rufipogon Griff, phylogeny, tissue Na tolerance",
author = "Solis, {Celymar Angela} and Yong, {Miing Tiem} and Gayatri Venkataraman and Paul Milham and Meixue Zhou and Lana Shabala and Paul Holford and Sergey Shabala and Chen, {Zhong Hua}",
note = "Funding Information: We would like to thank Dr. Anya Salih and Dr Rong Liu of the WSU Confocal Bio‐Imaging Facility, and Linda Westmoreland, Renee Smith, Craig Barton, Sharleen Hamersma, and Rosie Freeman for their excellent technical support. SunRice Australia and Hangzhou Normal University supplied all the plant materials used in the study. The work was supported by the Australian Department of Industry, Innovation and Science, Australian Government project to SS, MZ, LS, and ZHC. ZHC was supported by an Australian Research Council DECRA (DE140101143) grant and by Hort Innovation Australia Project (LP18000). Funding Information: We would like to thank Dr. Anya Salih and Dr Rong Liu of the WSU Confocal Bio-Imaging Facility, and Linda Westmoreland, Renee Smith, Craig Barton, Sharleen Hamersma, and Rosie Freeman for their excellent technical support. SunRice Australia and Hangzhou Normal University supplied all the plant materials used in the study. The work was supported by the Australian Department of Industry, Innovation and Science, Australian Government project to SS, MZ, LS, and ZHC. ZHC was supported by an Australian Research Council DECRA (DE140101143) grant and by Hort Innovation Australia Project (LP18000). Funding Information: Hort Innovation, Grant/Award Number: LP18000; Australian Research Council, Grant/Award Number: DE140101143; Department of Industry, Innovation and Science, Australian Government; Hangzhou Normal University Funding information Publisher Copyright: {\textcopyright} 2021 Scandinavian Plant Physiology Society",
year = "2021",
month = jul,
doi = "10.1111/ppl.13352",
language = "English",
volume = "172",
pages = "1594--1608",
journal = "Physiologia Plantarum",
issn = "0031-9317",
publisher = "Wiley-Blackwell",
number = "3",
}