Comparison of efficiency and time to regeneration of Agrobacterium-mediated transformation methods in Medicago truncatula

被引:10
|
作者
Wen, Li [1 ,2 ]
Chen, Yuanling [1 ,3 ]
Schnabel, Elise [1 ]
Crook, Ashley [1 ,4 ]
Frugoli, Julia [1 ]
机构
[1] Clemson Univ, Dept Genet & Biochem, Clemson, SC 29634 USA
[2] Changsha Univ Sci & Technol, Dept Food & Biol Engn, Changsha, Hunan, Peoples R China
[3] South China Agr Univ, Coll Life Sci, Guangzhou, Guangdong, Peoples R China
[4] Univ N Carolina, Dept Biol, Chapel Hill, NC 27599 USA
基金
美国国家科学基金会;
关键词
Medicago truncatula; Tissue culture regeneration; Root explants; crn Mutant; Cytokinin reporter; R108; A17; SOMATIC EMBRYOGENESIS; GENE-TRANSFER; TUMEFACIENS; ARABIDOPSIS; PLANTS; ROOTS; INFILTRATION; REPORTER; CULTURE; BAR;
D O I
10.1186/s13007-019-0404-1
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
BackgroundTissue culture transformation of plants has an element of art to it, with protocols passed on between labs but often not directly compared. As Medicago truncatula has become popular as a model system for legumes, rapid transformation is critical, and many protocols exist, with varying results.ResultsThe M. truncatula ecotypes, R108 and A17, were utilized to compare the effect of a modification to a previously used protocol based on shoot explants on the percentage of transformed plants produced from calli. This percentage was then compared to that of two additional transformation protocols based on root explants in the R108 ecotype. Variations in embryonic tissue sources, media components, time for transformation, and vectors were analyzed.ConclusionsWhile no A17 transgenic plants were obtained, transgenic plantlets from the R108 ecotype were produced in as little as 4 months with a comparison of the two widely studied ecotypes under a single set of conditions. While the protocols tested gave similar results in percentage of transformed plants produced, considerations of labor and time to transgenics that vary between the root explant protocols tested were discovered. These considerations may influence which protocol to choose for introducing a single transgene versus creating lines with multiple mutations utilizing a CRISPR/Cas9 construct.
引用
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页数:10
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