Highly efficient targeted mutagenesis in axolotl using Cas9 RNA-guided nuclease
Author(s) -
G. Parker Flowers,
Andrew T. Timberlake,
Kaitlin C. McLean,
James R. Monaghan,
Craig M. Crews
Publication year - 2014
Publication title -
development
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.15
H-Index - 36
eISSN - 1477-9129
pISSN - 0950-1991
DOI - 10.1242/dev.105072
Subject(s) - axolotl , biology , ambystoma mexicanum , brachyury , crispr , cas9 , genome editing , genetics , regeneration (biology) , zebrafish , mutagenesis , transcription activator like effector nuclease , rna , computational biology , microbiology and biotechnology , gene , mutation , embryonic stem cell , mesoderm
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.
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