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The Cbr-DPY-10(Arg92Cys) modification is a reliable co-conversion marker for CRISPR/Cas9 genome editing in Caenorhabditis briggsae

The maturation of genome editing techniques dramatically broadens the range of organisms amenable to mechanistic investigation. Caenorhabditis briggsae is a nematode species related to C. elegans and a favored target for comparative studies. Here, we expand the repertoire of co-conversion markers to...

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Autores principales: Toker, Itai Antoine, Hobert, Oliver
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Caltech Library 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9021883/
https://www.ncbi.nlm.nih.gov/pubmed/35622509
http://dx.doi.org/10.17912/micropub.biology.000554
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author Toker, Itai Antoine
Hobert, Oliver
author_facet Toker, Itai Antoine
Hobert, Oliver
author_sort Toker, Itai Antoine
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description The maturation of genome editing techniques dramatically broadens the range of organisms amenable to mechanistic investigation. Caenorhabditis briggsae is a nematode species related to C. elegans and a favored target for comparative studies. Here, we expand the repertoire of co-conversion markers to facilitate the screening and isolation of CRISPR/Cas9-edited lines in C. briggsae . Similar to its homologous C. elegans mutation, Cbr-dpy-10(Arg92Cys) is phenotypically easy to detect in its heterozygous form and is distinguishable from other combinations of Cbr-dpy- 10 alleles, a valuable feature for the reliable isolation of marker-free CRISPR/Cas9-edited animals.
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spelling pubmed-90218832022-04-22 The Cbr-DPY-10(Arg92Cys) modification is a reliable co-conversion marker for CRISPR/Cas9 genome editing in Caenorhabditis briggsae Toker, Itai Antoine Hobert, Oliver MicroPubl Biol Materials and Reagents The maturation of genome editing techniques dramatically broadens the range of organisms amenable to mechanistic investigation. Caenorhabditis briggsae is a nematode species related to C. elegans and a favored target for comparative studies. Here, we expand the repertoire of co-conversion markers to facilitate the screening and isolation of CRISPR/Cas9-edited lines in C. briggsae . Similar to its homologous C. elegans mutation, Cbr-dpy-10(Arg92Cys) is phenotypically easy to detect in its heterozygous form and is distinguishable from other combinations of Cbr-dpy- 10 alleles, a valuable feature for the reliable isolation of marker-free CRISPR/Cas9-edited animals. Caltech Library 2022-04-20 /pmc/articles/PMC9021883/ /pubmed/35622509 http://dx.doi.org/10.17912/micropub.biology.000554 Text en Copyright: © 2022 by the authors https://creativecommons.org/licenses/by/4.0/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.
spellingShingle Materials and Reagents
Toker, Itai Antoine
Hobert, Oliver
The Cbr-DPY-10(Arg92Cys) modification is a reliable co-conversion marker for CRISPR/Cas9 genome editing in Caenorhabditis briggsae
title The Cbr-DPY-10(Arg92Cys) modification is a reliable co-conversion marker for CRISPR/Cas9 genome editing in Caenorhabditis briggsae
title_full The Cbr-DPY-10(Arg92Cys) modification is a reliable co-conversion marker for CRISPR/Cas9 genome editing in Caenorhabditis briggsae
title_fullStr The Cbr-DPY-10(Arg92Cys) modification is a reliable co-conversion marker for CRISPR/Cas9 genome editing in Caenorhabditis briggsae
title_full_unstemmed The Cbr-DPY-10(Arg92Cys) modification is a reliable co-conversion marker for CRISPR/Cas9 genome editing in Caenorhabditis briggsae
title_short The Cbr-DPY-10(Arg92Cys) modification is a reliable co-conversion marker for CRISPR/Cas9 genome editing in Caenorhabditis briggsae
title_sort cbr-dpy-10(arg92cys) modification is a reliable co-conversion marker for crispr/cas9 genome editing in caenorhabditis briggsae
topic Materials and Reagents
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9021883/
https://www.ncbi.nlm.nih.gov/pubmed/35622509
http://dx.doi.org/10.17912/micropub.biology.000554
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