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Simple, rapid and efficient transformation of genotype Nisqually-1: a basic tool for the first sequenced model tree

Genotype Nisqually-1 is the first model woody plant with an available well-annotated genome. Nevertheless, a simple and rapid transformation of Nisqually-1 remains to be established. Here, we developed a novel shoot regeneration method for Nisqually-1 using leaf petiole and stem segment explants. Nu...

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Detalles Bibliográficos
Autores principales: Li, Shujuan, Zhen, Cheng, Xu, Wenjing, Wang, Chong, Cheng, Yuxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5453977/
https://www.ncbi.nlm.nih.gov/pubmed/28572673
http://dx.doi.org/10.1038/s41598-017-02651-x
Descripción
Sumario:Genotype Nisqually-1 is the first model woody plant with an available well-annotated genome. Nevertheless, a simple and rapid transformation of Nisqually-1 remains to be established. Here, we developed a novel shoot regeneration method for Nisqually-1 using leaf petiole and stem segment explants. Numerous shoots formed in the incision of explants within two weeks. The optimized shoot regeneration medium (SRM) contained 0.03 mg l(−1) 6-benzylaminopurine, 0.02 mg l(−1) indole-3-butyric acid and 0.0008 mg l(−1) thidiazuron. Based on this, Agrobacterium-mediated genetic transformation of stem explants was examined using the vector pBI(121) that contains the β-glucuronidase (GUS) as a reporter gene. Consequently, factors affecting transformation frequency of GUS-positive shoots were optimized as follows: Agrobacteria cell suspension with an OD(600) of 0.4, 20 min infection time, 2 days of co-cultivation duration and the addition of 80 µM acetosyringone into Agrobacteria infective suspension and co-cultivation SRM. Using this optimized method, transgenic plantlets of Nisqually-1 – with an average transformation frequency of 26.7% – were obtained with 2 months. Southern blot and GUS activity staining confirmed the integration of the foreign GUS gene into Nisqually-1. This novel transformation system for Nisqually-1 was rapid, efficient, and simple to operate and will improve more genetic applications in this model tree.