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利用 Cas9 RNA 引导的核酸酶在蝾螈中进行高效靶向诱变。

Highly efficient targeted mutagenesis in axolotl using Cas9 RNA-guided nuclease.

机构信息

Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT 06511, USA.

出版信息

Development. 2014 May;141(10):2165-71. doi: 10.1242/dev.105072. Epub 2014 Apr 24.

Abstract

Among tetrapods, only urodele salamanders, such as the axolotl Ambystoma mexicanum, can completely regenerate limbs as adults. The mystery of why salamanders, but not other animals, possess this ability has for generations captivated scientists seeking to induce this phenomenon in other vertebrates. Although many recent advances in molecular biology have allowed limb regeneration and tissue repair in the axolotl to be investigated in increasing detail, the molecular toolkit for the study of this process has been limited. Here, we report that the CRISPR-Cas9 RNA-guided nuclease system can efficiently create mutations at targeted sites within the axolotl genome. We identify individual animals treated with RNA-guided nucleases that have mutation frequencies close to 100% at targeted sites. We employ this technique to completely functionally ablate EGFP expression in transgenic animals and recapitulate developmental phenotypes produced by loss of the conserved gene brachyury. Thus, this advance allows a reverse genetic approach in the axolotl and will undoubtedly provide invaluable insight into the mechanisms of salamanders' unique regenerative ability.

摘要

在四足动物中,只有蝾螈,如墨西哥钝口螈 Ambystoma mexicanum,能够在成年时完全再生肢体。为什么蝾螈而不是其他动物具有这种能力,这个谜团让几代科学家着迷,他们试图在其他脊椎动物中诱导这种现象。尽管近年来分子生物学的许多进展使得能够更详细地研究蝾螈的肢体再生和组织修复,但用于研究这一过程的分子工具包一直受到限制。在这里,我们报告说,CRISPR-Cas9 RNA 引导的核酸酶系统可以有效地在蝾螈基因组中的靶向位点产生突变。我们鉴定出了个体动物,它们在靶向位点的突变频率接近 100%。我们利用这项技术在转基因动物中完全功能性地消除 EGFP 的表达,并重现了由保守基因 brachyury 缺失产生的发育表型。因此,这一进展使得在蝾螈中可以采用反向遗传学方法,无疑将为理解蝾螈独特再生能力的机制提供宝贵的见解。

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