The widely used Nicotiana benthamiana 16c line has an unusual T-DNA integration pattern including a transposon sequence

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Abstract

Nicotiana benthamiana is employed around the world for many types of research and one transgenic line has been used more extensively than any other. This line, 16c, expresses the Aequorea Victoria green fluorescent protein (GFP), highly and constitutively, and has been a major resource for visualising the mobility and actions of small RNAs. Insights into the mechanisms studied at a molecular level in N. benthamiana 16c are likely to be deeper and more accurate with a greater knowledge of the GFP gene integration site. Therefore, using next generation sequencing, genome mapping and local alignment, we identified the location and characteristics of the integrated T-DNA. As suggested from previous molecular hybridisation and inheritance data, the transgenic line contains a single GFP-expressing locus. However, the GFP coding sequence differs from that originally reported. Furthermore, a 3.2 kb portion of a transposon, appears to have co-integrated with the T-DNA. The location of the integration mapped to a region of the genome represented by Nbv0.5scaffold4905 in the www.benthgenome.com assembly, and with less integrity to Niben101Scf03641 in the www.solgenomics.net assembly. The transposon is not endogenous to laboratory strains of N. benthamiana or Agrobacterium tumefaciens strain GV3101 (MP90), which was reportedly used in the generation of line 16c. However, it is present in the popular LBA4404 strain. The integrated transposon sequence includes its 5' terminal repeat and a transposase gene, and is immediately adjacent to the GFP gene. This unexpected genetic arrangement may contribute to the characteristics that have made the 16c line such a popular research tool and alerts researchers, taking transgenic plants to commercial release, to be aware of this genomic hitchhiker.

Figures

  • Table 1. List of primers used in this study.
  • Fig 1. Schematic of pBIN19-mGFP-ER and Tn5393 and their integration site in 16c. (A–B) Schematic of genes within the T-DNA and transposon integrated in 16c genome. The sequence junctions between N. benthamiana genome-T-DNA-transposon-N. benthamiana genome are highlighted, GenBank accession number KY464890. (C) Log scale density plot of sequence reads aligning to T-DNA, transposon and flanking N. benthamiana genomic regions. (D) Location of primers used for amplification of various regions to confirm site of integration. (E) Log scale density plot of RNAseq reads aligning to T-DNA and transposon. (F) Gel image showing the endpoint (35 cycles) PCR amplicons of the T-DNA insert in 16c with LAB N. benthamiana used as a control. Expected sizes with primer pair B+E is 4174 nt and D+F is 4167 nt. NTC, no template control, 1 kb DNA Ladder (GeneRuler™). (G) Leaves of N. benthamiana 16c photographed under UV light, showing mobile silencing, 14 days after local induction of RNAi at a lower leaf. Abbreviations are: RB: Right Border, pNOS: nopaline synthase promoter, NPTII: neomycin phosphotransferase II encoding gene, tNOS: nopaline synthase terminator, p35S: Cauliflower mosaic virus 35S promoter. IR: inverted terminal repeat, tnpA transposase gene, res: recombination region, tnpR resolvase gene, IS1133: an insertion element, strA and strB: streptomycin resistance genes, Nb Genome: Flanking DNA of N. benthamiana.
  • Fig 2. Schematic showing the alignment of Sanger sequences to scaffolds in benthgenome.com and solgenomics.net.

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Philips, J. G., Naim, F., Lorenc, M. T., Dudley, K. J., Hellens, R. P., & Waterhouse, P. M. (2017). The widely used Nicotiana benthamiana 16c line has an unusual T-DNA integration pattern including a transposon sequence. PLoS ONE, 12(2). https://doi.org/10.1371/journal.pone.0171311

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