Targeted mutagenesis in the silkworm Bombyx mori using zinc finger nuclease mRNA injection

被引:141
作者
Takasu, Yoko [1 ,2 ,3 ]
Kobayashi, Isao [3 ]
Beumer, Kelly [4 ]
Uchino, Keiro [3 ]
Sezutsu, Hideki [3 ]
Sajwan, Suresh [1 ,2 ]
Carroll, Dana [4 ]
Tamura, Toshiki [3 ]
Zurovec, Michal [1 ,2 ]
机构
[1] Univ S Bohemia, Ctr Biol, Acad Sci, Ceske Budejovice 37005, Czech Republic
[2] Univ S Bohemia, Fac Nat Sci, Ceske Budejovice 37005, Czech Republic
[3] Natl Inst Agrobiol Sci, Tsukuba, Ibaraki 3058634, Japan
[4] Univ Utah, Sch Med, Dept Biochem, Salt Lake City, UT 84112 USA
关键词
Gene targeting; Nonhomologous end joining; Lepidoptera; BmBLOS2; Bm1; element; CAENORHABDITIS-ELEGANS; RESTRICTION ENZYMES; DROSOPHILA; CLEAVAGE; TRANSFORMATION; DOMAINS; REPAIR; WHITE;
D O I
10.1016/j.ibmb.2010.07.012
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
Targeted mutagenesis is one of the key methods for functional gene analysis. A simplified variant of gene targeting uses direct microinjection of custom-designed Zinc Finger Nuclease (ZFN) mRNAs into Drosophila embryos. To evaluate the applicability of this method to gene targeting in another insect, we mutagenized the Bombyx mori epidermal color marker gene BmBLOS2, which controls the formation of uric acid granules in the larval epidermis. Our results revealed that ZFN mRNA injection is effective to induce somatic, as well as germline, mutations in a targeted gene by non-homologous end joining (NHEJ). The ZFN-induced NHEJ mutations lack end-filling and blunt ligation products, and include mainly 7 bp or longer deletions, as well as single nucleotide insertions. These observations suggest that the B. moti double-strand break repair system relies on microhomologies rather than on a canonical ligase IV-dependent mechanism. The frequency of germline mutants in G(1) was sufficient to be used for gene targeting relying on a screen based solely on molecular methods. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:759 / 765
页数:7
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