Tip100转座子系统介导的medaka高效转基因。

IF 2 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Yoshitaka Tanaka, Takahide Seki, Atsushi Hoshino, Satoshi Ansai
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引用次数: 0

摘要

转座子介导的转基因是将外源DNA导入核基因组,建立稳定、高效表达遗传工具的转基因菌株的有效途径。虽然DNA转座子Tol2被广泛用于斑马鱼的转基因,但其内源性转座子活性可能导致非预期的转基因动员,使其不适合在米卡马(Oryzias latipes)中进行转基因。在这里,我们证明了DNA转座子Tip100,最初在常见的牵牛花(一种观赏植物)中发现,可以作为一个有用的转基因工具。当与Tip100转座酶mRNA共注射时,GFP转基因盒在注射鱼体细胞中的表达量显著增加。此外,被截断识别序列(每个截断100 bp)的转基因的表达水平与包含完整2.2 kb识别序列的原始载体相当。注射由种系特异性启动子驱动的转基因表明,注射Tip100 mRNA的鱼的种系传输率(42/68;62.7%)明显高于未注射该mRNA的鱼(13/62;21.0%)。我们成功地通过注射gfp阳性生殖细胞的异种杂交建立了转基因菌株(7/7;100%),并证明转基因基因被随机整合到medaka基因组中,在插入位点(hAT转座子超家族的插入标记)产生了8bp的重复。我们的研究结果表明,Tip100系统是一种很有前途的工具,可以在medaka和潜在的其他鱼类中产生稳定的表达各种遗传工具的转基因菌株。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Highly efficient transgenesis mediated by Tip100 transposon system in medaka.

Highly efficient transgenesis mediated by Tip100 transposon system in medaka.

Highly efficient transgenesis mediated by Tip100 transposon system in medaka.

Highly efficient transgenesis mediated by Tip100 transposon system in medaka.

Transgenesis mediated by transposon is an effective approach for introducing exogenous DNA into the nuclear genome and establishing stable transgenic strains that efficiently express genetic tools. Although the DNA transposon Tol2 is widely used for transgenesis in zebrafish, its endogenous transpositional activity can lead to unintended transgene mobilization, making it unsuitable for transgenesis in medaka (Oryzias latipes). Here, we demonstrated that the DNA transposon Tip100, originally identified in the common morning glory (Ipomoea purpurea), an ornamental plant, can serve as a useful tool for transgenesis in Japanese medaka. The GFP transgene cassette, when co-injected with Tip100 transposase mRNA, was expressed in significantly higher number of somatic cells in the injected fish. Furthermore, a transgene flanked by truncated recognition sequences (100 bp each) exhibited expression levels comparable to those of the original vector containing the full 2.2 kb recognition sequence. Injection of a transgene driven by a germline-specific promoter revealed that fish injected with Tip100 mRNA exhibited a significantly higher germline transmission rate (42/68; 62.7%) compared to those injected without the mRNA (13/62; 21.0%). We successfully established transgenic strains by outcrossing injected founders with GFP-positive germ cells (7/7; 100%) and demonstrated that the transgenes were randomly integrated into the medaka genome, generating 8-bp duplications at the insertional sites-an insertional signature of the hAT superfamily of transposons. Our findings indicate that the Tip100 system is a promising tool for generating stable transgenic strains that express various genetic tools in medaka and potentially other fish species.

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来源期刊
Transgenic Research
Transgenic Research 生物-生化研究方法
CiteScore
5.40
自引率
0.00%
发文量
38
审稿时长
4-8 weeks
期刊介绍: Transgenic Research focusses on transgenic and genome edited higher organisms. Manuscripts emphasizing biotechnological applications are strongly encouraged. Intellectual property, ethical issues, societal impact and regulatory aspects also fall within the scope of the journal. Transgenic Research aims to bridge the gap between fundamental and applied science in molecular biology and biotechnology for the plant and animal academic and associated industry communities. Transgenic Research publishes -Original Papers -Reviews: Should critically summarize the current state-of-the-art of the subject in a dispassionate way. Authors are requested to contact a Board Member before submission. Reviews should not be descriptive; rather they should present the most up-to-date information on the subject in a dispassionate and critical way. Perspective Reviews which can address new or controversial aspects are encouraged. -Brief Communications: Should report significant developments in methodology and experimental transgenic higher organisms
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