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

被引:75
作者
Flowers, G. Parker [1 ]
Timberlake, Andrew T. [1 ]
Mclean, Kaitlin C. [1 ]
Monaghan, James R. [2 ]
Crews, Craig M. [1 ,3 ,4 ]
机构
[1] Yale Univ, Dept Mol Cellular & Dev Biol, New Haven, CT 06511 USA
[2] Northeastern Univ, Dept Biol, Boston, MA 02115 USA
[3] Yale Univ, Dept Chem, New Haven, CT 06511 USA
[4] Yale Univ, Dept Pharmacol, New Haven, CT 06511 USA
来源
DEVELOPMENT | 2014年 / 141卷 / 10期
基金
美国国家卫生研究院;
关键词
Axolotl; CRISPR; Regeneration; Mutagenesis; GENE; LIMB; TRANSCRIPTION; IDENTIFICATION; REGENERATION; BRACHYURY; CELLS; PCR;
D O I
10.1242/dev.105072
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
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.
引用
收藏
页码:2165 / 2171
页数:7
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