Improved cotton transformation protocol mediated by Agrobacterium and biolistic combined-methods

农杆菌 生物 转化(遗传学) 转基因 转基因作物 分生组织 胚胎发生 转化效率 植物 细胞生物学 胚胎 开枪 遗传学 基因 胚胎发生
作者
Thuanne Pires Ribeiro,Isabela Tristan Lourenço‐Tessutti,Bruno Paes de Melo,Carolina Vianna Morgante,Alvaro Salles Filho,Camila Barrozo Jesus Lins,Gilanna Falcão Ferreira,Glênia Nunes Mello,Leonardo Lima Pepino de Macedo,Wagner Alexandre Lucena,Maria Cristina Mattar Silva,O. B. Oliveira-Neto,Maria Fátima Grossi‐de‐Sá
出处
期刊:Planta [Springer Science+Business Media]
卷期号:254 (2) 被引量:10
标识
DOI:10.1007/s00425-021-03666-5
摘要

The combined Agrobacterium- and biolistic-mediated methods of cotton transformation provide a straightforward and highly efficient protocol for obtaining transgenic cotton. Cotton (Gossypium spp.) is the most important crop for natural textile fiber production worldwide. Nonetheless, one of the main challenges in cotton production are the losses resulting from insect pests, pathogens, and abiotic stresses. One effective way to solve these issues is to use genetically modified (GM) varieties. Herein, we describe an improved protocol for straightforward and cost-effective genetic transformation of cotton embryo axes, merging biolistics and Agrobacterium. The experimental steps include (1) Agrobacterium preparation, (2) seed sterilization, (3) cotton embryo excision, (4) lesion of shoot-cells by tungsten bombardment, (5) Agrobacterium-mediated transformation, (6) embryo co-culture, (7) regeneration and selection of transgenic plants in vitro, and (8) molecular characterization of plants. Due to the high regenerative power of the embryonic axis and the exceptional ability of the meristem cells for plant regeneration through organogenesis in vitro, this protocol can be performed in approximately 4–10 weeks, with an average plant regeneration of about 5.5% (± 0.53) and final average transformation efficiency of 60% (± 0.55). The transgene was stably inherited, and most transgenic plants hold a single copy of the transgene, as desirable and expected in Agrobacterium-mediated transformation. Additionally, the transgene was stably expressed over generations, and transgenic proteins could be detected at high levels in the T2 generation of GM cotton plants. The T2 progeny showed no phenotypic or productivity disparity compared to wild-type plants. Collectively, the use of cotton embryo axes and the enhanced DNA-delivery system by combining particle bombardment and Agrobacterium infection enabled efficient transgenic plant recovery, overcoming usual limitations associated with the recalcitrance of several cotton genotypes subjected to somatic embryogenesis. The improved approach states this method’s success for cotton genetic modification, allowing us to obtain GM cotton plants carrying traits, which are of fundamental relevance for the advancement of global agribusiness.
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