Cargando…

Iterative editing of multiple genes using CRISPR/Cas9 in C. elegans

Certain sets of genes are derived from gene duplication and share substantial sequence similarity in C. elegans , presenting a significant challenge in determining the specific roles of each gene and their collective impact on cellular processes. Here, we show that a collection of genes can be disru...

Descripción completa

Detalles Bibliográficos
Autores principales: Pu, Longjun, Nilsson, Lars, Chen, Changchun, Wang, Jing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Caltech Library 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10685264/
https://www.ncbi.nlm.nih.gov/pubmed/38033425
http://dx.doi.org/10.17912/micropub.biology.000898
_version_ 1785151592251523072
author Pu, Longjun
Nilsson, Lars
Chen, Changchun
Wang, Jing
author_facet Pu, Longjun
Nilsson, Lars
Chen, Changchun
Wang, Jing
author_sort Pu, Longjun
collection PubMed
description Certain sets of genes are derived from gene duplication and share substantial sequence similarity in C. elegans , presenting a significant challenge in determining the specific roles of each gene and their collective impact on cellular processes. Here, we show that a collection of genes can be disrupted in a single animal via multiple rounds of CRISPR/Cas9 mediated genome editing. We found that up to three genes can be simultaneously disrupted in a single editing event with high efficiency. Our approach offers an opportunity to explore the genetic interaction and molecular underpinning of gene clusters with redundant function.
format Online
Article
Text
id pubmed-10685264
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Caltech Library
record_format MEDLINE/PubMed
spelling pubmed-106852642023-11-30 Iterative editing of multiple genes using CRISPR/Cas9 in C. elegans Pu, Longjun Nilsson, Lars Chen, Changchun Wang, Jing MicroPubl Biol New Method Certain sets of genes are derived from gene duplication and share substantial sequence similarity in C. elegans , presenting a significant challenge in determining the specific roles of each gene and their collective impact on cellular processes. Here, we show that a collection of genes can be disrupted in a single animal via multiple rounds of CRISPR/Cas9 mediated genome editing. We found that up to three genes can be simultaneously disrupted in a single editing event with high efficiency. Our approach offers an opportunity to explore the genetic interaction and molecular underpinning of gene clusters with redundant function. Caltech Library 2023-11-14 /pmc/articles/PMC10685264/ /pubmed/38033425 http://dx.doi.org/10.17912/micropub.biology.000898 Text en Copyright: © 2023 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 New Method
Pu, Longjun
Nilsson, Lars
Chen, Changchun
Wang, Jing
Iterative editing of multiple genes using CRISPR/Cas9 in C. elegans
title Iterative editing of multiple genes using CRISPR/Cas9 in C. elegans
title_full Iterative editing of multiple genes using CRISPR/Cas9 in C. elegans
title_fullStr Iterative editing of multiple genes using CRISPR/Cas9 in C. elegans
title_full_unstemmed Iterative editing of multiple genes using CRISPR/Cas9 in C. elegans
title_short Iterative editing of multiple genes using CRISPR/Cas9 in C. elegans
title_sort iterative editing of multiple genes using crispr/cas9 in c. elegans
topic New Method
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10685264/
https://www.ncbi.nlm.nih.gov/pubmed/38033425
http://dx.doi.org/10.17912/micropub.biology.000898
work_keys_str_mv AT pulongjun iterativeeditingofmultiplegenesusingcrisprcas9incelegans
AT nilssonlars iterativeeditingofmultiplegenesusingcrisprcas9incelegans
AT chenchangchun iterativeeditingofmultiplegenesusingcrisprcas9incelegans
AT wangjing iterativeeditingofmultiplegenesusingcrisprcas9incelegans