Directed genome engineering for genome optimization

被引:8
作者
D'Halluin, Kathleen [1 ]
Ruiter, Rene [1 ]
机构
[1] Bayer CropSci NV, B-9052 Ghent, Belgium
关键词
DNA double strand break induction and repair; site-specific nuclease; genome editing; crop improvement; DOUBLE-STRAND BREAKS; HOMOLOGOUS RECOMBINATION; TRANSGENE EXPRESSION; TARGETED MUTAGENESIS; GENE INTEGRATION; PLANT-CELLS; DNA; RNA; FREQUENCY; TRANSFORMATION;
D O I
10.1387/ijdb.130217kd
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The ability to develop nucleases with tailor-made activities for targeted DNA double-strand break induction at will at any desired position in the genome has been a major breakthrough to make targeted genome optimization feasible in plants. The development of site specific nucleases for precise genome modification has expanded the repertoire of tools for the development and optimization of traits, already including mutation breeding, molecular breeding and transgenesis. Through directed genome engineering technology, the huge amount of information provided by genomics and systems biology can now more effectively be used for the creation of plants with improved or new traits, and for the dissection of gene functions. Although still in an early phase of deployment, its utility has been demonstrated for engineering disease resistance, herbicide tolerance, altered metabolite profiles, and for molecular trait stacking to allow linked transmission of transgenes. In this article, we will briefly review the different approaches for directed genome engineering with the emphasis on double strand break (DSB)-mediated engineering towards genome optimization for crop improvement and towards the acceleration of functional genomics.
引用
收藏
页码:621 / 627
页数:7
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