3
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Overexpression of GmMYB14 improves high‐density yield and drought tolerance of soybean through regulating plant architecture mediated by the brassinosteroid pathway

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Summary

          MYB transcription factors (TFs) have been reported to regulate the biosynthesis of secondary metabolites, as well as to mediate plant adaption to abiotic stresses, including drought. However, the roles of MYB TFs in regulating plant architecture and yield potential remain poorly understood. Here, we studied the roles of the dehydration‐inducible GmMYB14 gene in regulating plant architecture, high‐density yield and drought tolerance through the brassinosteroid (BR) pathway in soybean. GmMYB14 was shown to localize to nucleus and has a transactivation activity. Stable GmMYB14‐overexpressing ( GmMYB14‐OX) transgenic soybean plants displayed a semi‐dwarfism and compact plant architecture associated with decreased cell size, resulting in a decrease in plant height, internode length, leaf area, leaf petiole length and leaf petiole angle, and improved yield in high density under field conditions. Results of the transcriptome sequencing suggested the involvement of BRs in regulating GmMYB14‐OX plant architecture. Indeed, GmMYB14‐OX plants showed reduced endogenous BR contents, while exogenous application of brassinolide could partly rescue the phenotype of GmMYB14‐OX plants. Furthermore, GmMYB14 was shown to directly bind to the promoter of GmBEN1 and up‐regulate its expression, leading to reduced BR content in GmMYB14‐OX plants. GmMYB14‐OX plants also displayed improved drought tolerance under field conditions. GmBEN1 expression was also up‐regulated in the leaves of GmMYB14‐OX plants under polyethylene glycol treatment, indicating that the GmBEN1‐mediated reduction in BR level under stress also contributed to drought/osmotic stress tolerance of the transgenic plants. Our findings provided a strategy for stably increasing high‐density yield and drought tolerance in soybean using a single TF‐encoding gene.

          Related collections

          Most cited references53

          • Record: found
          • Abstract: found
          • Article: not found

          Arabidopsis mesophyll protoplasts: a versatile cell system for transient gene expression analysis.

          The transient gene expression system using Arabidopsis mesophyll protoplasts has proven an important and versatile tool for conducting cell-based experiments using molecular, cellular, biochemical, genetic, genomic and proteomic approaches to analyze the functions of diverse signaling pathways and cellular machineries. A well-established protocol that has been extensively tested and applied in numerous experiments is presented here. The method includes protoplast isolation, PEG-calcium transfection of plasmid DNA and protoplast culture. Physiological responses and high-throughput capability enable facile and cost-effective explorations as well as hypothesis-driven tests. The protoplast isolation and DNA transfection procedures take 6-8 h, and the results can be obtained in 2-24 h. The cell system offers reliable guidelines for further comprehensive analysis of complex regulatory mechanisms in whole-plant physiology, immunity, growth and development.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Rapid, transient expression of fluorescent fusion proteins in tobacco plants and generation of stably transformed plants.

            Expression and tracking of fluorescent fusion proteins has revolutionized our understanding of basic concepts in cell biology. The protocol presented here has underpinned much of the in vivo results highlighting the dynamic nature of the plant secretory pathway. Transient transformation of tobacco leaf epidermal cells is a relatively fast technique to assess expression of genes of interest. These cells can be used to generate stable plant lines using a more time-consuming, cell culture technique. Transient expression takes from 2 to 4 days whereas stable lines are generated after approximately 2 to 4 months.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Regulation of OsSPL14 by OsmiR156 defines ideal plant architecture in rice.

              Increasing crop yield is a major challenge for modern agriculture. The development of new plant types, which is known as ideal plant architecture (IPA), has been proposed as a means to enhance rice yield potential over that of existing high-yield varieties. Here, we report the cloning and characterization of a semidominant quantitative trait locus, IPA1 (Ideal Plant Architecture 1), which profoundly changes rice plant architecture and substantially enhances rice grain yield. The IPA1 quantitative trait locus encodes OsSPL14 (SOUAMOSA PROMOTER BINDING PROTEIN-LIKE 14) and is regulated by microRNA (miRNA) OsmiR156 in vivo. We demonstrate that a point mutation in OsSPL14 perturbs OsmiR156-directed regulation of OsSPL14, generating an 'ideal' rice plant with a reduced tiller number, increased lodging resistance and enhanced grain yield. Our study suggests that OsSPL14 may help improve rice grain yield by facilitating the breeding of new elite rice varieties.
                Bookmark

                Author and article information

                Contributors
                son.tran@ttu.edu
                zhouxinan@caas.cn
                caodong@caas.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
                23 November 2020
                April 2021
                : 19
                : 4 ( doiID: 10.1111/pbi.v19.4 )
                : 702-716
                Affiliations
                [ 1 ] Key Laboratory of Biology and Genetic Improvement of Oil Crops Ministry of Agriculture and Rural Affairs Oil Crops Research Institute Chinese Academy of Agricultural Sciences Wuhan China
                [ 2 ] The Industrial Crop Institute Shanxi Academy of Agricultural Sciences Taiyuan China
                [ 3 ] Institute of Genomics for Crop Abiotic Stress Tolerance Department of Plant and Soil Science Texas Tech University Lubbock TX USA
                [ 4 ] Stress Adaptation Research Unit RIKEN Center for Sustainable Resource Science Tsurumi Yokohama Japan
                Author notes
                [*] [* ] Correspondence (Tel +1 806‐834‐7829; Fax +1 806‐742‐4521; email: son.tran@ 123456ttu.edu (L.‐S.P.T.); Tel +86‐27‐ 86711563; fax +86‐27‐86816451; email: zhouxinan@ 123456caas.cn (X.Z.); Tel +86 27 86711563; Fax +86 27 86816451; email: caodong@ 123456caas.cn (D.C.))

                [†]

                Limiao Chen and Hongli Yang are equally contributed to this work.

                Author information
                https://orcid.org/0000-0002-0607-6263
                https://orcid.org/0000-0001-9883-9768
                https://orcid.org/0000-0003-3446-5669
                Article
                PBI13496
                10.1111/pbi.13496
                8051608
                33098207
                30e7d2a5-5684-4fd7-9fc1-49801983bc31
                © 2020 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
                : 14 May 2020
                : 18 October 2020
                Page count
                Figures: 7, Tables: 0, Pages: 15, Words: 10988
                Funding
                Funded by: National Genetically Modified Organisms Breeding Major Projects
                Award ID: 2016ZX08004‐002 and 2016ZX08004‐005
                Funded by: National Natural Science Foundation of China
                Award ID: 32072087 and 31701455
                Funded by: Opening Project of the Key Laboratory of Oil Crop Biology and Genetics Breeding, Ministry of Agriculture
                Award ID: KF2018007
                Funded by: Modern Agro‐industry Technology Research Platform, Soybean Agro‐industry Technology Research Platform
                Award ID: CARS‐04
                Funded by: The Science and technology innovation project of Chinese Academy of Agricultural Sciences, Molecular Mechanism Analysis and Germplasm Innovation of Soybean Stress Resistance to Tolerance and Nutrient Efficient Utilization
                Award ID: CAAS‐ASTIP‐2016‐OCRI
                Funded by: Central Public‐interest Scientific Institution Basal Research Fund
                Award ID: 1610172018008
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                April 2021
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.0.2 mode:remove_FC converted:16.04.2021

                Biotechnology
                plant architecture,drought tolerance,myb transcription factor,soybean,yield,brassinosteroids

                Comments

                Comment on this article