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      The lipid transfer protein OsLTPL159 is involved in cold tolerance at the early seedling stage in rice

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          Summary

          Nonspecific lipid transfer proteins (ns LTPs) play critical roles in plant development and response to abiotic stresses. Here, we found that a rice lipid transfer protein, Os LTPL159, was associated with cold tolerance at the early seedling stage. Overexpression of an Os LTPL159 IL 112 allele from the cold‐tolerant introgression line IL112 in either the japonica variety Zhonghua17 ( ZH17) or the indica variety Teqing background dramatically enhanced cold tolerance. In addition, down‐regulation of the expression of Os LTPL159 in the japonica variety ZH17 by RNA interference ( RNAi) significantly decreased cold tolerance. Further transcriptomic, physiological and histological analysis showed that the Os LTPL159 IL 112 allele likely enhanced the cold tolerance of rice at the early seedling stage by decreasing the toxic effect of reactive oxygen species, enhancing cellulose deposition in the cell wall and promoting osmolyte accumulation, thereby maintaining the integrity of the chloroplasts. Notably, overexpression of another allele, Os LTPL159 GC 2, from the recipient parent Guichao 2 ( GC2), an indica variety, did not improve cold tolerance, indicating that the variations in the Os LTPL159 coding region of GC2 might disrupt its function for cold tolerance. Further sequence comparison found that all 22 japonica varieties surveyed had an Os LTPL159 haplotype identical to IL112 and were more cold‐tolerant than the surveyed indica varieties, implying that the variations in Os LTPL159 might be associated with differential cold tolerance of japonica and indica rice. Therefore, our findings suggest that the Os LTPL159 allele of japonica rice could be used to improve cold tolerance of indica rice through a molecular breeding strategy.

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          Control of root system architecture by DEEPER ROOTING 1 increases rice yield under drought conditions.

          The genetic improvement of drought resistance is essential for stable and adequate crop production in drought-prone areas. Here we demonstrate that alteration of root system architecture improves drought avoidance through the cloning and characterization of DEEPER ROOTING 1 (DRO1), a rice quantitative trait locus controlling root growth angle. DRO1 is negatively regulated by auxin and is involved in cell elongation in the root tip that causes asymmetric root growth and downward bending of the root in response to gravity. Higher expression of DRO1 increases the root growth angle, whereby roots grow in a more downward direction. Introducing DRO1 into a shallow-rooting rice cultivar by backcrossing enabled the resulting line to avoid drought by increasing deep rooting, which maintained high yield performance under drought conditions relative to the recipient cultivar. Our experiments suggest that control of root system architecture will contribute to drought avoidance in crops.
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            COLD1 confers chilling tolerance in rice.

            Rice is sensitive to cold and can be grown only in certain climate zones. Human selection of japonica rice has extended its growth zone to regions with lower temperature, while the molecular basis of this adaptation remains unknown. Here, we identify the quantitative trait locus COLD1 that confers chilling tolerance in japonica rice. Overexpression of COLD1(jap) significantly enhances chilling tolerance, whereas rice lines with deficiency or downregulation of COLD1(jap) are sensitive to cold. COLD1 encodes a regulator of G-protein signaling that localizes on plasma membrane and endoplasmic reticulum (ER). It interacts with the G-protein α subunit to activate the Ca(2+) channel for sensing low temperature and to accelerate G-protein GTPase activity. We further identify that a SNP in COLD1, SNP2, originated from Chinese Oryza rufipogon, is responsible for the ability of COLD(jap/ind) to confer chilling tolerance, supporting the importance of COLD1 in plant adaptation.
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              Cell wall remodeling under abiotic stress

              Plants exposed to abiotic stress respond to unfavorable conditions on multiple levels. One challenge under drought stress is to reduce shoot growth while maintaining root growth, a process requiring differential cell wall synthesis and remodeling. Key players in this process are the formation of reactive oxygen species (ROS) and peroxidases, which initially cross-link phenolic compounds and glycoproteins of the cell walls causing stiffening. The function of ROS shifts after having converted all the peroxidase substrates in the cell wall. If ROS-levels remain high during prolonged stress, OH°-radicals are formed which lead to polymer cleavage. In concert with xyloglucan modifying enzymes and expansins, the resulting cell wall loosening allows further growth of stressed organs.
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                Author and article information

                Contributors
                liufx@cau.edu.cn
                Journal
                Plant Biotechnol J
                Plant Biotechnol. J
                10.1111/(ISSN)1467-7652
                PBI
                Plant Biotechnology Journal
                John Wiley and Sons Inc. (Hoboken )
                1467-7644
                1467-7652
                11 September 2019
                March 2020
                : 18
                : 3 ( doiID: 10.1111/pbi.v18.3 )
                : 756-769
                Affiliations
                [ 1 ] State Key Laboratory of Plant Physiology and Biochemistry National Center for Evaluation of Agricultural Wild Plants (Rice) MOE Laboratory of Crop Heterosis and Utilization Beijing Key Laboratory of Crop Genetic Improvement Department of Plant Genetics and Breeding China Agricultural University Beijing China
                Author notes
                [*] [* ] Correspondence (Tel 86 10 62732540; fax 86 10 62732540; email liufx@ 123456cau.edu.cn )
                Author information
                https://orcid.org/0000-0003-4312-8429
                Article
                PBI13243
                10.1111/pbi.13243
                7004919
                31469486
                42ac8fb2-f6f5-4062-8686-7f7bb6c37891
                © 2019 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 17 December 2018
                : 03 August 2019
                : 15 August 2019
                Page count
                Figures: 7, Tables: 0, Pages: 14, Words: 9932
                Funding
                Funded by: National Natural Science Foundation of China , open-funder-registry 10.13039/501100001809;
                Award ID: 31671647
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                March 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.7.5 mode:remove_FC converted:06.02.2020

                Biotechnology
                lipid transfer protein,cold tolerance,early seedling stage,rice
                Biotechnology
                lipid transfer protein, cold tolerance, early seedling stage, rice

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