Directed, efficient, and versatile modifications of the Drosophila genome by genomic engineering

被引:373
作者
Huang, Juan [1 ]
Zhou, Wenke [1 ]
Dong, Wei [1 ]
Watson, Annie M. [1 ]
Hong, Yang [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Cell Biol & Physiol, Pittsburgh, PA 15261 USA
基金
美国国家卫生研究院;
关键词
cell polarity; ends-out targeting; homologous recombination; phiC31; integrase; MEDIATED CASSETTE EXCHANGE; HOMOLOGOUS RECOMBINATION; TRANSGENIC DROSOPHILA; TARGETED MUTAGENESIS; ENDS-OUT; MELANOGASTER; INTEGRASE; POLARITY; PHI-C31; CONSTRUCTION;
D O I
10.1073/pnas.0900641106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
070301 [无机化学]; 070403 [天体物理学]; 070507 [自然资源与国土空间规划学]; 090105 [作物生产系统与生态工程];
摘要
With the completion of genome sequences of major model organisms, increasingly sophisticated genetic tools are necessary for investigating the complex and coordinated functions of genes. Here we describe a genetic manipulation system termed "genomic engineering'' in Drosophila. Genomic engineering is a 2-step process that combines the ends-out (replacement) gene targeting with phage integrase phi C31-mediated DNA integration. First, through an improved and modified gene targeting method, a founder knockout line is generated by deleting the target gene and replacing it with an integration site of phi C31. Second, DNA integration by phi C31 is used to reintroduce modified target-gene DNA into the native locus in the founder knock-out line. Genomic engineering permits directed and highly efficient modifications of a chosen genomic locus into virtually any desired mutant allele. We have successfully applied the genomic engineering scheme on 6 different genes and have generated at their loci more than 70 unique alleles.
引用
收藏
页码:8284 / 8289
页数:6
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