Fister Andrew S, Shi Zi, Zhang Yufan, Helliwell Emily E, Maximova Siela N, Guiltinan Mark J
The Huck Institutes of the Life Sciences, The Pennsylvania State University, 422 Life Sciences Building, University Park, PA 16802 USA.
Center for Applied Genetic Technologies, University of Georgia, Athens, GA 30602 USA.
Plant Methods. 2016 Mar 11;12:19. doi: 10.1186/s13007-016-0119-5. eCollection 2016.
Theobroma cacao L., the source of cocoa, is a crop of significant economic value around the world. To facilitate the study of gene function in cacao we have developed a rapid Agrobacterium-mediated transient genetic transformation protocol. Here we present a detailed methodology for our transformation assay, as well as an assay for inoculation of cacao leaves with pathogens.
Agrobacterium tumefaciens cultures are induced then vacuum-infiltrated into cacao leaves. Transformation success can be gauged 48 h after infiltration by observation of green fluorescent protein and by qRT-PCR. We clarify the characteristics of cacao leaf stages and demonstrate that our strategy efficiently transforms leaves of developmental stage C. The transformation protocol has high efficacy in stage C leaves of four of eight tested genotypes. We also present the functional analysis of cacao chitinase overexpression using the transient transformation system, which resulted in decreased pathogen biomass and lesion size after infection with Phytophthora tropicalis.
Leaves expressing transgenes of interest can be used in subsequent functional genetic assays such as pathogen bioassay, metabolic analysis, gene expression analysis etc. This transformation protocol can be carried out in 1 day, and the transgenes expressing leaf tissue can be maintained in petri dishes for 5-7 days, allowing sufficient time for performance of additional downstream gene functional analysis. Application of these methods greatly increases the rapidity with which candidate genes with roles in defense can be tested.
可可树(Theobroma cacao L.)是可可的来源,是一种在全球具有重要经济价值的作物。为了便于研究可可中的基因功能,我们开发了一种快速的农杆菌介导的瞬时遗传转化方案。在此,我们展示了转化测定的详细方法,以及用病原体接种可可叶片的测定方法。
诱导根癌农杆菌培养物,然后真空渗入可可叶片。在渗入后48小时,通过观察绿色荧光蛋白和定量逆转录聚合酶链反应(qRT-PCR)可以评估转化是否成功。我们阐明了可可叶片阶段的特征,并证明我们的策略能有效地转化发育阶段C的叶片。该转化方案在八个测试基因型中的四个的C阶段叶片中具有高效性。我们还展示了使用瞬时转化系统对可可几丁质酶过表达的功能分析,结果表明在用热带疫霉感染后,病原体生物量和病斑大小有所减少。
表达感兴趣的转基因的叶片可用于后续的功能遗传测定,如病原体生物测定、代谢分析、基因表达分析等。这种转化方案可以在一天内完成,表达转基因的叶片组织可以在培养皿中保存5至7天,为进行额外的下游基因功能分析留出足够的时间。这些方法的应用大大提高了对具有防御作用的候选基因进行测试的速度。