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TALEN 电穿孔介导的组织特异性和普遍基因敲除为研究海鞘基因功能提供了新方法。

Tissue-specific and ubiquitous gene knockouts by TALEN electroporation provide new approaches to investigating gene function in Ciona.

机构信息

Shimoda Marine Research Center, University of Tsukuba, Shimoda, Shizuoka, 415-0025, Japan.

出版信息

Development. 2014 Jan;141(2):481-7. doi: 10.1242/dev.099572. Epub 2013 Dec 18.

Abstract

Custom designed nucleases can simplify gene targeting experiments and have the potential to allow these techniques to be performed in a wide range of organisms. Transcriptional activator-like effector nucleases (TALENs) are starting to fulfill this potential with the advantages of low cost and fast construction times. Here, we report that TALENs are highly effective at inducing mutations in specific genomic loci in the ascidian chordate Ciona intestinalis. In Ciona there are well-established methods to introduce exogenous DNA by electroporation, and we show that this method can be used to introduce constructs that can express TALENs ubiquitously or in specific tissues. Our current protocols enable the rapid analysis of hundreds of TALEN-induced mutants. TALEN electroporations result in a high rate of mutations. These mutations can result in gene knockouts that recapitulate previously described functions of Fgf3 and Hox12. We show that TALENs can work efficiently to cause tissue-specific knockouts and demonstrate this by knocking out Hox12 in the epidermis and Fgf3 in neural tissues. We also use tissue-specific knockouts to reveal a new function of Fgf3 during ascidian larval metamorphosis.

摘要

定制设计的核酸酶可以简化基因靶向实验,并有可能使这些技术在广泛的生物体中得以实施。转录激活子样效应核酸酶(TALENs)具有成本低和构建时间快的优势,开始发挥这种潜力。在这里,我们报告 TALENs 在诱导环节动物海鞘的特定基因组位点突变方面非常有效。在海鞘中,通过电穿孔引入外源 DNA 的方法已经建立,我们表明这种方法可用于引入可在全身或特定组织中表达 TALEN 的构建体。我们目前的方案使快速分析数百个 TALEN 诱导的突变体成为可能。TALEN 电穿孔导致突变率很高。这些突变可以导致基因敲除,重现先前描述的 Fgf3 和 Hox12 功能。我们表明 TALENs 可以有效地进行组织特异性敲除,并通过在表皮中敲除 Hox12 和在神经组织中敲除 Fgf3 来证明这一点。我们还利用组织特异性敲除来揭示 Fgf3 在环节动物幼虫变态过程中的新功能。

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