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  5. Developing biocontainment strategies to suppress transgene escape via pollen dispersal from transgenic plants
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Developing biocontainment strategies to suppress transgene escape via pollen dispersal from transgenic plants

Date Issued
August 1, 2011
Author(s)
Moon, Hong Seok
Advisor(s)
C. Neal Stewart, Jr.
Additional Advisor(s)
Robert M. Augé
Arnold M. Saxton
Zong-Ming Cheng
Feng Chen
Permanent URI
https://trace.tennessee.edu/handle/20.500.14382/19190
Abstract

Genetic engineering is important to enhance crop characteristics and certain traits. Genetically engineered crop cultivation brings environmental and ecological concerns with the potential of unwanted transgene escape and introgression. Transgene escape has been considered as a major environmental and regulatory concern. This concern could be alleviated by appropriate biocontainment strategies. Therefore, it is important to develop efficient and reliable biocontainment strategies.


Removing transgenes from pollen has been known to be the most environmentally friendly biocontainment strategy. A transgene excision vector containing a codon optimized serine resolvase CinH recombinase (CinH) and its recognition sites RS2 were constructed and transformed into tobacco (Nicotiana tabacum cv. Xanthi). In this system, the pollen-specific LAT52 promoter from tomato was employed to control the expression of CinH recombinase. Loss of expression of a green fluorescent protein (GFP) gene under the control of the LAT59 promoter from tomato was used as an indicator of transgene excision. Efficiency of transgene excision from pollen was determined by flow cytometry (FCM)-based pollen screening. While a transgenic event in the absence of CinH recombinase contained about 70% of GFP-synthesizing pollen, three single-copy transgene events contained less than 1% of GFP-synthesizing pollen based on 30,000 pollen grains analyzed per event. This suggests that CinH-RS2 recombination system could be effectively utilized for transgene biocontainment.

A novel approach for selective male sterility in pollen was developed and evaluated as a biocontainment strategy. Overexpression of the EcoRI restriction endonuclease caused pollen ablation and/or infertility in tobacco, but exhibited normal phenotypes when compared to non-transgenic tobacco. Three EcoRI contained 0% GFP positive pollen, while GFP control plants contained 64% GFP positive pollen based on 9,000 pollen grains analyzed by flow cytometry-based transgenic pollen screening method. However, seven EcoRI events appeared to have 100% efficiency on selective male sterility based on the test-crosses. The results suggested that this selective male sterility could be used as a highly efficient and reliable biocontainment strategy for genetically engineered crop cultivation.

Subjects

Biocontainment

Pollen

Transgene excision

Site-Specific Recombi...

Selective Male Steril...

Restriction Endonucle...

Disciplines
Plant Biology
Degree
Doctor of Philosophy
Major
Plants, Soils, and Insects
Embargo Date
December 1, 2011
File(s)
Thumbnail Image
Name

MoonHongSeokdissertation.pdf

Size

7.6 MB

Format

Adobe PDF

Checksum (MD5)

15a1203b180ebe46a2fee072af3642e2

Thumbnail Image
Name

Moon_Dissertation.doc

Size

4.36 MB

Format

Microsoft Word

Checksum (MD5)

dba2970aaeddbc5050817e3c974a623d


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