TY - JOUR
T1 - Streptothricin acetyl transferase 2 (Sat2)
T2 - A dominant selection marker for Caenorhabditis elegans genome editing
AU - Obinata, Hiroyuki
AU - Sugimoto, Asako
AU - Niwa, Shinsuke
N1 - Funding Information:
This work was supported by the Japan Society for the Promotion of Science, Grant numbers: 16H06536 and 17H05010 (https://www. jsps.go.jp); the Naito Foundation (https://www. naito-f.or.jp/jp/index.php); and the Brain Science Foundation (http://www.bs-f.jp/kenjo.html). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The authors wish to thank members of the Sugimoto laboratory at Tohoku University, Japan. We also thank Sandra Cheesman, PhD, from Edanz Group (www.edanzediting.com/ac) for editing a draft of this manuscript. The N2 strain was provided by the CGC, which is funded by the NIH Program P40 OD010440.
Publisher Copyright:
© 2018 Obinata et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
PY - 2018/5
Y1 - 2018/5
N2 - Studies on Caenorhabditis elegans would benefit from the introduction of new selectable markers to allow more complex types of experiments to be conducted with this model animal. We established a new antibiotic selection marker for C. elegans transformation based on nourseothricin (NTC) and its resistance-encoding gene, streptothricin-acetyl transferase 2 (Sat2). NTC was able to efficiently prevent worm development at very low concentrations, and the worms expressing Sat2 were able to survive on the selection plates without any developmental defects. Using CRISPR/Cas9 and NTC selection, we were able to easily insert a 13-kb expression cassette into a defined locus in C. elegans. The structure and spectrum of NTC differs from other antibiotics like hygromycin B and geneticin, making it possible to use NTC alongside them. Indeed, we confirmed NTC-sat2 selection could work with the hygromycin B selection system simultaneously. Thus, the new NTC–Sat2 system can act as a useful dominant marker for gene transfer and genome editing in C. elegans.
AB - Studies on Caenorhabditis elegans would benefit from the introduction of new selectable markers to allow more complex types of experiments to be conducted with this model animal. We established a new antibiotic selection marker for C. elegans transformation based on nourseothricin (NTC) and its resistance-encoding gene, streptothricin-acetyl transferase 2 (Sat2). NTC was able to efficiently prevent worm development at very low concentrations, and the worms expressing Sat2 were able to survive on the selection plates without any developmental defects. Using CRISPR/Cas9 and NTC selection, we were able to easily insert a 13-kb expression cassette into a defined locus in C. elegans. The structure and spectrum of NTC differs from other antibiotics like hygromycin B and geneticin, making it possible to use NTC alongside them. Indeed, we confirmed NTC-sat2 selection could work with the hygromycin B selection system simultaneously. Thus, the new NTC–Sat2 system can act as a useful dominant marker for gene transfer and genome editing in C. elegans.
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U2 - 10.1371/journal.pone.0197128
DO - 10.1371/journal.pone.0197128
M3 - Article
C2 - 29742140
AN - SCOPUS:85046806076
SN - 1932-6203
VL - 13
JO - PLoS ONE
JF - PLoS ONE
IS - 5
M1 - e0197128
ER -