News section
home news forum careers events suppliers solutions markets resources directories advertise contacts
 

A highly efficient 'genetically modified gene-deletor' system to remove all functional transgenes from pollen, seed or both
January, 2007

Source: Plant Biotechnology Journal, Blackwell Synergy

'GM-gene-deletor': fused loxP-FRT recognition sequences dramatically improve the efficiency of FLP or CRE recombinase on transgene excision from pollen and seed of tobacco plants
Keming Luo, Hui Duan, Degang Zhao, Xuelian Zheng, Wei Deng, Yongqin Chen, C. Neal Stewart Jr, Richard McAvoy, Xiangning Jiang, Yanhong Wu, Aigong He, Yan Pei, Yi Li

Plant Biotechnology Journal (OnlineEarly Articles).
doi:10.1111/j.1467-7652.2006.00237.x
http://www.blackwell-synergy.com/doi/abs/10.1111/j.1467-7652.2006.00237.x

SUMMARY

Pollen- and seed-mediated transgene flow is a concern in plant biotechnology. We report here a highly efficient 'genetically modified (GM)-gene-deletor' system to remove all functional transgenes from pollen, seed or both. With the three pollen- and/or seed-specific gene promoters tested, the phage CRE/loxP or yeast FLP/FRT system alone was inefficient in excising transgenes from tobacco pollen and/or seed, with no transgenic event having 100% efficiency. When loxP-FRT fusion sequences were used as recognition sites, simultaneous expression of both FLP and CRE reduced the average excision efficiency, but the expression of FLP or CRE alone increased the average excision efficiency, with many transgenic events being 100% efficient based on more than 25 000 T1 progeny examined per event. The 'GM-gene-deletor' reported here may be used to produce 'non-transgenic' pollen and/or seed from transgenic plants and to provide a bioconfinement tool for transgenic crops and perennials, with special applicability towards vegetatively propagated plants and trees.

Article: http://www.blackwell-synergy.com/doi/abs/10.1111/j.1467-7652.2006.00237.x

News release

Other news from this source

18,260

Back to main news page

The news release or news item on this page is copyright © 2007 by the organization where it originated.
The content of the SeedQuest website is copyright © 1992-2007 by SeedQuest - All rights reserved
Fair Use Notice