| Autor: |
Cooper CA; CSIRO Health and Biosecurity, Australian Animal Health Laboratory, Geelong, VIC, Australia., Challagulla A; CSIRO Health and Biosecurity, Australian Animal Health Laboratory, Geelong, VIC, Australia., Jenkins KA; CSIRO Health and Biosecurity, Australian Animal Health Laboratory, Geelong, VIC, Australia., Wise TG; CSIRO Health and Biosecurity, Australian Animal Health Laboratory, Geelong, VIC, Australia., O'Neil TE; CSIRO Health and Biosecurity, Australian Animal Health Laboratory, Geelong, VIC, Australia., Morris KR; CSIRO Health and Biosecurity, Australian Animal Health Laboratory, Geelong, VIC, Australia., Tizard ML; CSIRO Health and Biosecurity, Australian Animal Health Laboratory, Geelong, VIC, Australia., Doran TJ; CSIRO Health and Biosecurity, Australian Animal Health Laboratory, Geelong, VIC, Australia. Timothy.Doran@csiro.au. |
| Abstrakt: |
Generating transgenic and gene edited mammals involves in vitro manipulation of oocytes or single cell embryos. Due to the comparative inaccessibility of avian oocytes and single cell embryos, novel protocols have been developed to produce transgenic and gene edited birds. While these protocols are relatively efficient, they involve two generation intervals before reaching complete somatic and germline expressing transgenic or gene edited birds. Most of this work has been done with chickens, and many protocols require in vitro culturing of primordial germ cells (PGCs). However, for many other bird species no methodology for long term culture of PGCs exists. Developing methodologies to produce germline transgenic or gene edited birds in the first generation would save significant amounts of time and resource. Furthermore, developing protocols that can be readily adapted to a wide variety of avian species would open up new research opportunities. Here we report a method using sperm as a delivery mechanism for gene editing vectors which we call sperm transfection assisted gene editing (STAGE). We have successfully used this method to generate GFP knockout embryos and chickens, as well as generate embryos with mutations in the doublesex and mab-3 related transcription factor 1 (DMRT1) gene using the CRISPR/Cas9 system. The efficiency of the method varies from as low as 0% to as high as 26% with multiple factors such as CRISPR guide efficiency and mRNA stability likely impacting the outcome. This straightforward methodology could simplify gene editing in many bird species including those for which no methodology currently exists. |
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