Plant Genome Engineering with Sequence-Specific Nucleases

被引:290
作者
Voytas, Daniel F. [1 ,2 ]
机构
[1] Univ Minnesota, Dept Genet Cell Biol & Dev, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Ctr Genome Engn, Minneapolis, MN 55455 USA
来源
ANNUAL REVIEW OF PLANT BIOLOGY, VOL 64 | 2013年 / 64卷
基金
美国国家科学基金会;
关键词
zinc-finger nucleases; transcription activator-like effector nucleases; TALENs; meganucleases; nonhomologous end joining; homologous recombination; gene targeting; DOUBLE-STRAND BREAKS; ZINC-FINGER NUCLEASES; DNA-BINDING SPECIFICITY; TARGETED GENE ADDITION; HOMOLOGOUS RECOMBINATION; TAL EFFECTORS; T-DNA; EFFICIENT CONSTRUCTION; TRANSGENE INTEGRATION; HOMING ENDONUCLEASES;
D O I
10.1146/annurev-arplant-042811-105552
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Recent advances in genome engineering provide newfound control over a plant's genetic material. It is now possible for most bench scientists to alter DNA in living plant cells in a variety of ways, including introducing specific nucleotide substitutions in a gene that change a protein's amino acid sequence, deleting genes or chromosomal segments, and inserting foreign DNA at precise genomic locations. Such targeted DNA sequence modifications are enabled by sequence-specific nucleases that create double-strand breaks in the genomic loci to be altered. The repair of the breaks, through either homologous recombination or nonhomologous end joining, can be controlled to achieve the desired sequence modification. Genome engineering promises to advance basic plant research by linking DNA sequences to biological function. Further, genome engineering will enable plants' biosynthetic capacity to be harnessed to produce the many agricultural products required by an expanding world population.
引用
收藏
页码:327 / 350
页数:24
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