Development of selectable marker-free transgenic rice plants with enhanced seed tocopherol content through FLP/FRT-mediated spontaneous auto-excision

23Citations
Citations of this article
26Readers
Mendeley users who have this article in their library.

Abstract

Development of marker-free transgenic plants is a technical alternative for avoiding concerns about the safety of selectable marker genes used in genetically modified (GM) crops. Here, we describe the construction of a spontaneous self-excision binary vector using an oxidative stress-inducible modified FLP/FRT system and its successful application to produce marker-free transgenic rice plants with enhanced seed tocopherol content. To generate selectable marker-free transgenic rice plants, we constructed a binary vector using the hpt selectable marker gene and the rice codon-optimized FLP (mFLP) gene under the control of an oxidative stress-inducible promoter between two FRT sites, along with multiple cloning sites for convenient cloning of genes of interest. Using this pCMF binary vector with the NtTC gene, marker-free T1 transgenic rice plants expressing NtTC were produced by Agrobacterium-mediated stable transformation using hygromycin as a selective agent, followed by segregation of selectable marker genes. Furthermore, α-, γ-, and total tocopherol levels were significantly increased in seeds of the marker-free transgenic TC line compared with those of wild-type plants. Thus, this spontaneous auto-excision system, incorporating an oxidative stress-inducible mFLP/FRT system to eliminate the selectable marker gene, can be easily adopted and used to efficiently generate marker-free transgenic rice plants. Moreover, nutritional enhancement of rice seeds through elevation of tocopherol content coupled with this marker-free strategy may improve human health and public acceptance of GM rice.

Figures

  • Fig 1. Schematic diagram of the T-DNA region of binary vectors for marker elimination and an DNA excised product. Restriction sites within the MCS were unique digestion sites in the vector. The structure of pCMF was the same to as of pHWMF except that the modified FLP gene was replaced with the native FLP gene. pCMF-TC was derived from inserting theNtTC gene, which is a tocopherol cyclase ortholog isolated from tobacco, into multiple cloning sites of pCMF. After gene excision, the CaMV 35S promoter was inserted adjacent to the NtTC coding region. P35SF, HPTR, and TCR primers were designed to detect the DNA excision. The PCR product amplified with P35SF/TCR would be 1.5 kb if DNA excision occurred and 5.7 kb otherwise. P35S, CaMV 35S gene promoter; hpt, hygromycin phosphotransferase gene; T35S, 35S CaMV gene terminator; Ppod, stress-inducible peroxidase gene promoter; FLP; recombinase gene from Saccharomyces cerevisiae; Tnos: Agrobacterium nopaline synthase gene terminator; MCS, multiple cloning site; LB, left border; RB, right border; NtTC, tocopherol cyclase gene isolated from tobacco; FRT, FLP recognition site.
  • Table 1. Differences in codon usage betweenOryza sativa, native FLP, and S. cerevisiae and codons used formFLP gene synthesis.
  • Fig 2. PCR and sequencing analysis for identification of transgenes and gene excision in transgenic T0 plants. (a) PCR results with the primer pair P35S/TCR using the genomic DNAs prepared from fresh leaves of transgenic plants after regeneration. (b) Sequence analysis to confirm gene excision from the genome of transgenic T0 plants. The PCR fragments amplified using the primers P35S and TCR were sequenced. (c) PCR results with the primer sets P35SF/HTPR and P35SF/TCR using genomic DNAs prepared from the mature leaves of five randomly selected transgenic T0 lines. M, molecular marker. Line numbers are indicated at the top of each lane.
  • Fig 3. Southern blot analysis of T1 progenies of the transgenic lines.Genomic DNA was digested with EcoRV, which created one cut in pCMF-TC, and hybridized with the DIG-labeled NtTC (a) or hpt (b) probe. M, DIG-labeled molecular marker; P, positive control; lanes 1–5, progenies of the TC2 line; lanes 6–8, progenies of the TC3 line.
  • Fig 4. Identification of the T-DNA in transgenic rice plants to select marker-free transgenic rice lines. (a) PCR analysis of T1 transgenic rice plants for marker excision. (b) RT-PCR analysis ofNtTC and hpt from leaves of T1 transgenic rice plants. The rice tubulin (tub) gene was used for normalization.
  • Fig 5. Germination test of T1 progenies derived from the transgenic lines. Seeds of the transgenic primary plants and nontransgenic wild-type plants were sown on germination medium containing hygromycin or without antibiotics.
  • Fig 6. Tocopherol contents from seeds of marker-free transgenic rice plants and wild-type rice plants. Black and gray bars correspond to transgenic TC3-1 plants and wild-type rice plants. Values are means ± SDs (n = 5), and student’s t tests were used to compare values obtained from transgenic lines to those of the wild-type plants. ** p < 0.01.
  • Fig 7. Schematic showing the production of selectable marker-free transgenic rice.

References Powered by Scopus

Rapid isolation of high molecular weight plant DNA

10455Citations
N/AReaders
Get full text

Vitamin E Consumption and the Risk of Coronary Disease in Women

1989Citations
N/AReaders
Get full text

Agrobacterium-mediated plant transformation: The biology behind the "gene-jockeying" tool

1055Citations
N/AReaders
Get full text

Cited by Powered by Scopus

Molecular breeding technologies and strategies for rust resistance in wheat (Triticum aestivum) for sustained food security

49Citations
N/AReaders
Get full text

A high-capacity gene stacking toolkit for the oleaginous microalga, Nannochloropsis oceanica CCMP1779

46Citations
N/AReaders
Get full text

The current status and development of insect-resistant genetically engineered poplar in china

40Citations
N/AReaders
Get full text

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Cite

CITATION STYLE

APA

Woo, H. J., Qin, Y., Park, S. Y., Park, S. K., Cho, Y. G., Shin, K. S., … Cho, H. S. (2015). Development of selectable marker-free transgenic rice plants with enhanced seed tocopherol content through FLP/FRT-mediated spontaneous auto-excision. PLoS ONE, 10(7). https://doi.org/10.1371/journal.pone.0132667

Readers over time

‘15‘16‘17‘18‘19‘20‘21‘22‘23‘24‘2501234

Readers' Seniority

Tooltip

PhD / Post grad / Masters / Doc 9

56%

Researcher 7

44%

Readers' Discipline

Tooltip

Agricultural and Biological Sciences 12

67%

Biochemistry, Genetics and Molecular Bi... 5

28%

Engineering 1

6%

Article Metrics

Tooltip
Social Media
Shares, Likes & Comments: 1

Save time finding and organizing research with Mendeley

Sign up for free
0