Homing endonucleases catalyze double-stranded DNA breaks and somatic transgene excision in Aedes aegypti

被引:21
作者
Traver, B. E. [1 ]
Anderson, M. A. E. [1 ]
Adelman, Z. N. [1 ]
机构
[1] Virginia Polytech Inst & State Univ, Dept Entomol, Fralin Life Sci Inst 305, Blacksburg, VA 24061 USA
关键词
Aedes aegypti; homing endonuclease; Sindbis virus; gap repair; YELLOW-FEVER MOSQUITO; GREEN FLUORESCENT PROTEIN; TARGETED GENE KNOCKOUT; ZINC-FINGER NUCLEASES; HOMOLOGOUS RECOMBINATION; I-CREI; MAMMALIAN-CELLS; SINDBIS VIRUS; HIGH-EFFICIENCY; DROSOPHILA;
D O I
10.1111/j.1365-2583.2009.00905.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Aedes aegypti is a major vector of arthropod-borne viruses such as yellow fever virus and dengue viruses. Efforts to discern the function of genes involved in important behaviours, such as vector competence and host seeking through reverse genetics, would greatly benefit from the ability to generate targeted gene disruptions. Homing endonucleases are selfish elements which catalyze double-stranded DNA (dsDNA) breaks in a sequence-specific manner. In this report we demonstrate that the homing endonucleases I-PpoI, I-SceI, I-CreI and I-AniI are all able to induce dsDNA breaks in adult female Ae. aegypti chromosomes as well as catalyze the somatic excision of a transgene. These experiments provide evidence that homing endonucleases can be used to manipulate the genome of this important disease vector.
引用
收藏
页码:623 / 633
页数:11
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