|
|
|
Development and identification of glyphosate-tolerant transgenic soybean via direct selection with glyphosate |
GUO Bing-fu1, 2, HONG Hui-long1, HAN Jia-nan1, ZHANG Li-juan1, LIU Zhang-xiong1, GUO Yong1, QIU Li-juan1 |
1 National Key Facility for Crop Gene Resources and Genetic Improvement (NFCRI)/MOA Key Lab of Soybean Biology/Institute of Crop Sciences, Chinese Academy of Agricultural Sciences, Beijing 100081, P.R.China
2 Jiangxi Province Key Laboratory of Oilcrops Biology/Crops Research Institute, Jiangxi Academy of Agricultural Sciences, Nanchang 330200, P.R.China |
|
|
Abstract Glyphosate-tolerant soybean is the most widely planted genetically modified crop worldwide. However, soybean remains recalcitrant to routine transformation because of the low infection efficiency of Agrobacterium to soybean and lack of useful selectable markers. In this study, several Agrobacterium strains and cell densities were compared by transient expression of the GUS gene. The results showed that Agrobacterium strain Ag10 at cell densities of OD600 of 0.6–0.9 yielded the highest infection efficiency in Agrobacterium-mediated soybean cotyledonary node transformation system. Meanwhile, a simple and rapid method was developed for identification of glyphosate tolerance in putative T0 transgenic plants, consisting of spotting plantlets with 1 µL Roundup®. The whole cycle of genetic transformation could be shortened to about 3 mon by highly efficient selection with glyphosate during the transformation process and application of the spot assay in putative T0 transgenic plantlets. The transformation frequency ranged from 2.9 to 5.6%. This study provides an improved protocol for development and identification of glyphosate-tolerant transgenic soybeans.
|
Received: 04 January 2019
Accepted:
|
Fund: This work was supported by the National Natural Science Foundation of China (31601326), the National Transgenic Major Program of China (2016ZX08004001 and 2016ZX08011003), and the China Postdoctoral Science Foundation (2016M591300). |
Corresponding Authors:
Correspondence QIU Li-juan, Tel/Fax: +86-10-82105840, E-mail: qiulijuan@caas.cn; GUO Yong, Tel/Fax: +86-10-82105840, E-mail: guoyong@caas.cn
|
About author:
GUO Bing-fu, E-mail: gbfhq@163.com; |
Cite this article:
GUO Bing-fu, HONG Hui-long, HAN Jia-nan, ZHANG Li-juan, LIU Zhang-xiong, GUO Yong, QIU Li-juan.
2020.
Development and identification of glyphosate-tolerant transgenic soybean via direct selection with glyphosate. Journal of Integrative Agriculture, 19(5): 1186-1196.
|
Bowen B A. 1993. Markers for plant gene transfer. In: Kung S, Wu R, eds., Transgenic Plants: Engineering and Utilization. Academic Press, San Diego. pp. 89–123.
Clemente T E, LaVallee B J, Howe A R, Conner-Ward D, Rozman R J, Hunter P E, Broyles D L, Kasten D S, Hinchee M A. 2000. Progeny analysis of glyphosate selected transgenic soybeans derived from Agrobacterium-mediated transformation. Crop Science, 40, 797–803.
Dang W, Wei Z M. 2007. An optimized Agrobacterium-mediated transformation for soybean for expression of binary insect resistance genes. Plant Science, 173, 381–389.
Di R, Purcell V, Collins G B, Ghabrial S A. 1996. Production of transgenic soybean lines expressing the bean pod mottle virus coat protein precursor gene. Plant Cell Reports, 15, 746–750.
Dill G M, CaJacob C A, Padgette S R. 2008. Glyphosate-resistant crops: Adoption, use and future considerations. Pest Management Science, 64, 326–331.
Donaldson P A, Simmonds D H. 2000. Susceptibility to Agrobacterium tumefaciens and cotyledonary node transformation in short-season soybean. Plant Cell Reports, 8, 923–929.
Dun B Q, Wang X J, Lu W, Chen M, Zhang W, Ping S Z, Wang Z X, Zhang B M, Lin M. 2014. Development of highly glyphosate-tolerant tobacco by coexpression of glyphosate acetyltransferase gat and G2-aroA genes. The Crop Journal, 2, 164–169.
Green J M. 2014. Current state of herbicides in herbicide-resistant crops. Pest Management Science, 70, 1351–1357.
Green J M, Owen M D K. 2011. Herbicide-resistant crops: Utilities and limitations for herbicide-resistant weed management. Journal of Agricultural and Food Chemistry, 59, 5819–5829.
Guo B F, Guo Y, Hong H L, Jin L G, Zhang L J, Chang R Z, Lu W, Lin M, Qiu L J. 2015a. Co-expression of G2-EPSPS and glyphosate acetyltransferase GAT genes conferring high tolerance to glyphosate in soybean. Frontier in Plant Science, 6, 8.
Guo B F, Ma Y S, Zhang L J, Hong H L, Chang R Z, Guo Y, Qiu L J. 2015b. Assessment of Agrobacterium sensitivity for different soybean genotypes and suitable germplasm screening. Plant Genetic Research, 16, 569–575. (in Chinese)
Hartman G L, West E D, Herman T K. 2011. Crops that feed the world 2. Soybean-worldwide production, use, and constraints caused by pathogens and pests. Food Security, 3, 5–17.
He F X, Lang Z H, Lu W, Lin M, Zhang J, Huang D F. 2008. The establishment of maize transformation system with a glyphosate-tolerant 2mG2-epsps gene as a selectable marker. Biotechnology Bulletin, 5, 92–97. (in Chinese)
Hinchee M A W, Connor D V, Newell C A, McDonnell R E, Sato S J, Gasser C S, Fischhoff D A, Re D B, Fraley R T, Horsch R B. 1988. Production of transgenic soybean plants using Agrobacterium-mediated DNA transfer. Nature Biotechnology, 6, 915–922.
Howe A R, Gasser C S, Brown S M, Padgette S R, Hart J, Parker G B, Fromm M E, Armstrong C L. 2002. Glyphosate as a selective agent for the production of fertile transgenic maize (Zea mays L.) plants. Molceular Breeding, 10, 153–164.
Jefferson R A, Kavanagh T A, Bevan N W. 1987. GUS fusions: β-glucuronidase as a sensitive and versatile gene fusion market in higher plants. EMBO Journal, 6, 3901–3907.
Lazo G R, Stein P A, Ludwig R A. 1991. A DNA transformation-competent Arabidopsis genomic library in Agrobacterium. Biotechnology, 9, 963–967.
Li S E, Cong Y H, Liu Y P, Wang T T, Shuai Q, Chen N, Gai J Y, Li Y. 2017. Optimization of Agrobacterium-mediated transformation in soybean. Frontier in Plant Science, 8, 246.
Liu Y J, Zhang Y W, Liu Y, Lu W, Wang G Y. 2015. Metabolic effects of glyphosate on transgenic maize expressing a G2-EPSPS gene from Pseudomonas fluorescens. Journal of Plant Biochemistry and Biotechnology, 24, 233–241.
Lu L H, Han Q, Li L, Zhou L, Liu R F, Song Z Y, Shen Z C, Shou H X. 2014. Establishment of an efficient transformation protocol for soybean using glyphosate as selective agent and the development of glyphosate-tolerant transgenic soybean lines. Scientia Sinica (Vitae), 44, 406–415. (in Chinese)
Macabe D E, Swain W F, Martinen B J, Christou P. 1988. Stable transformation of soybean (Glycine max) by particle acceleration. Nature Biotechnology, 6, 923–929.
Marra M C, Piggott N E, Carlson G A. 2004. The Net Benefits, Including Convenience, of Roundup Ready Soybeans: Results from a National Survey. NSF Center for Integrated Pest Management, Technical Bull Raleigh NC.
Murray M G, Thompson W F. 1980. Rapid isolation of high molecular weight plant DNA. Nucletic Acids Research, 8, 4321–4325.
Olhoft P M, Flagel L X, Donovan C M, Somers D A. 2003. Efficient soybean transformation using hygromycin B selection in the cotyledonary-node method. Planta, 216, 723–735.
Padgette S, Kolacz K, Delannay X. 1995. Development, identification and characterization of a glyphosate-tolerant soybean event. Crop Science, 35, 1451–1461.
Park S H, Rose S C, Zapata C, Srivatanakul M, Smith R H. 1998. Cross-protection and selectable marker genes in plant transformation. In Vitro Cell Development-Plant, 34, 117–121.
Paz M M, Shou H X, Guo Z B, Zhang Z Y, Banerjee A K, Wang K. 2004. Assessment of conditions affecting Agrobacterium-mediated soybean transformation using the cotyledonary node explants. Euphytica, 136, 167–179.
Rech E L, Vianna G R, Aragao F J L. 2008. High-efficiency transformation by biolistics of soybean, common bean and cotton transgenic plants. Nature Protocol, 3, 410–418.
Reddy M S S, Dinkins R D, Collins G B. 2003. Gene silencing in transgenic soybean plants transformed via particle bombardment. Plant Cell Reports, 21, 676–683.
Singh H B, Singh B N, Singh S P, Nautiyal C S. 2010. Solid-state cultivation of trichoderma harzianum NBRI-1055 for modulating natural antioxidants in soybean seed matrix. Bioresource Technology, 101, 6444–6453.
Soto N, Delgado C, Hernández Y, Rosabal Y, Ferreira A, Pujol M, Agagao F J L, Enriquez G A. 2017. Efficient particle bombardment-mediated transformation of Cuban soybean (INCASoy-36) using glyphosate as a selective agent. Plant Cell Tissue and Organ Culture, 128, 187–196.
Tan S, Evans R, Singh B. 2006. Herbicidal inhibitors of amino acid biosynthesis and herbicide-tolerant crops. Amino Acids, 30, 195–204.
Trick H N, Finer J J. 1988. Sonication-assisted Agrobacterium-mediated transformation of soybean (Glycine max (L.) Merrill) embryogenic suspension culture tissue. Plant Cell Reports, 17, 482–488.
Trick H N, Finer J J. 1997. SAAT: Sonication-assisted Agrobacterium-mediated transformation. Transgenic Research, 6, 329–337.
Yamada T, Takagi K, Ishimoto M. 2012. Recent advantages in soybean transformation and their application to molecular breeding and genomic analysis. Breeding Science, 61, 480–494.
Yao T H. 2009. Chemical weeding in the soybean field. Journal of Shanxi Agricultural Sciences, 37, 96–97. (in Chinese)
Zhang Z, Xing A, Staswick P, Clemente T. 1999. The use of glufosinate as a selective agent in Agrobacterium-mediated transformation of soybean. Plant Cell Tissue and Organ Culture, 56, 37–46.
Zhong G C. 2007. Establishment of high efficient regenration system of Lilium and Agrobacterium-mediated genetic transformation. MSc thesis, Southwest University, China. (in Chinese)
Zhou H, Arrowsmith J W, Fromm M E, Hironaka C M, Taylor M L, Rodriguez D, Pajeau M E, Brown S M, Santino C G, Fry J E. 1995. Glyphosate tolerant CP4 and Gox gene as a selectable marker in wheat transformation. Plant Cell Reports, 15, 159–163.
|
No Suggested Reading articles found! |
|
|
Viewed |
|
|
|
Full text
|
|
|
|
|
Abstract
|
|
|
|
|
Cited |
|
|
|
|
|
Shared |
|
|
|
|
|
Discussed |
|
|
|
|