Cargando…
ErCas12a CRISPR-MAD7 for Model Generation in Human Cells, Mice, and Rats
MAD7 is an engineered class 2 type V-A CRISPR-Cas (Cas12a/Cpf1) system isolated from Eubacterium rectale. Analogous to Cas9, it is an RNA-guided nuclease with demonstrated gene editing activity in Escherichia coli and yeast cells. Here, we report that MAD7 is capable of generating indels and fluores...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Mary Ann Liebert, Inc., publishers
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7194332/ https://www.ncbi.nlm.nih.gov/pubmed/32315227 http://dx.doi.org/10.1089/crispr.2019.0068 |
_version_ | 1783528325792137216 |
---|---|
author | Liu, Zhenyi Schiel, John A. Maksimova, Elena Strezoska, Žaklina Zhao, Guojun Anderson, Emily M. Wu, Yumei Warren, Joe Bartels, Angela van Brabant Smith, Anja Lowe, Chris E. Forbes, Kevin P. |
author_facet | Liu, Zhenyi Schiel, John A. Maksimova, Elena Strezoska, Žaklina Zhao, Guojun Anderson, Emily M. Wu, Yumei Warren, Joe Bartels, Angela van Brabant Smith, Anja Lowe, Chris E. Forbes, Kevin P. |
author_sort | Liu, Zhenyi |
collection | PubMed |
description | MAD7 is an engineered class 2 type V-A CRISPR-Cas (Cas12a/Cpf1) system isolated from Eubacterium rectale. Analogous to Cas9, it is an RNA-guided nuclease with demonstrated gene editing activity in Escherichia coli and yeast cells. Here, we report that MAD7 is capable of generating indels and fluorescent gene tagging of endogenous genes in human HCT116 and U2OS cancer cell lines, respectively. In addition, MAD7 is highly proficient in generating indels, small DNA insertions (23 bases), and larger integrations ranging from 1 to 14 kb in size in mouse and rat embryos, resulting in live-born transgenic animals. Due to the different protospacer adjacent motif requirement, small-guide RNA, and highly efficient targeted gene disruption and insertions, MAD7 can expand the CRISPR toolbox for genome enginnering across different systems and model organisms. |
format | Online Article Text |
id | pubmed-7194332 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Mary Ann Liebert, Inc., publishers |
record_format | MEDLINE/PubMed |
spelling | pubmed-71943322020-05-04 ErCas12a CRISPR-MAD7 for Model Generation in Human Cells, Mice, and Rats Liu, Zhenyi Schiel, John A. Maksimova, Elena Strezoska, Žaklina Zhao, Guojun Anderson, Emily M. Wu, Yumei Warren, Joe Bartels, Angela van Brabant Smith, Anja Lowe, Chris E. Forbes, Kevin P. CRISPR J Research Articles MAD7 is an engineered class 2 type V-A CRISPR-Cas (Cas12a/Cpf1) system isolated from Eubacterium rectale. Analogous to Cas9, it is an RNA-guided nuclease with demonstrated gene editing activity in Escherichia coli and yeast cells. Here, we report that MAD7 is capable of generating indels and fluorescent gene tagging of endogenous genes in human HCT116 and U2OS cancer cell lines, respectively. In addition, MAD7 is highly proficient in generating indels, small DNA insertions (23 bases), and larger integrations ranging from 1 to 14 kb in size in mouse and rat embryos, resulting in live-born transgenic animals. Due to the different protospacer adjacent motif requirement, small-guide RNA, and highly efficient targeted gene disruption and insertions, MAD7 can expand the CRISPR toolbox for genome enginnering across different systems and model organisms. Mary Ann Liebert, Inc., publishers 2020-04-01 2020-04-21 /pmc/articles/PMC7194332/ /pubmed/32315227 http://dx.doi.org/10.1089/crispr.2019.0068 Text en © Zhenyi Liu et al. 2020; Published by Mary Ann Liebert, Inc. This Open Access article is distributed under the terms of the Creative Commons Attribution Noncommercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and the source are cited. |
spellingShingle | Research Articles Liu, Zhenyi Schiel, John A. Maksimova, Elena Strezoska, Žaklina Zhao, Guojun Anderson, Emily M. Wu, Yumei Warren, Joe Bartels, Angela van Brabant Smith, Anja Lowe, Chris E. Forbes, Kevin P. ErCas12a CRISPR-MAD7 for Model Generation in Human Cells, Mice, and Rats |
title | ErCas12a CRISPR-MAD7 for Model Generation in Human Cells, Mice, and Rats |
title_full | ErCas12a CRISPR-MAD7 for Model Generation in Human Cells, Mice, and Rats |
title_fullStr | ErCas12a CRISPR-MAD7 for Model Generation in Human Cells, Mice, and Rats |
title_full_unstemmed | ErCas12a CRISPR-MAD7 for Model Generation in Human Cells, Mice, and Rats |
title_short | ErCas12a CRISPR-MAD7 for Model Generation in Human Cells, Mice, and Rats |
title_sort | ercas12a crispr-mad7 for model generation in human cells, mice, and rats |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7194332/ https://www.ncbi.nlm.nih.gov/pubmed/32315227 http://dx.doi.org/10.1089/crispr.2019.0068 |
work_keys_str_mv | AT liuzhenyi ercas12acrisprmad7formodelgenerationinhumancellsmiceandrats AT schieljohna ercas12acrisprmad7formodelgenerationinhumancellsmiceandrats AT maksimovaelena ercas12acrisprmad7formodelgenerationinhumancellsmiceandrats AT strezoskazaklina ercas12acrisprmad7formodelgenerationinhumancellsmiceandrats AT zhaoguojun ercas12acrisprmad7formodelgenerationinhumancellsmiceandrats AT andersonemilym ercas12acrisprmad7formodelgenerationinhumancellsmiceandrats AT wuyumei ercas12acrisprmad7formodelgenerationinhumancellsmiceandrats AT warrenjoe ercas12acrisprmad7formodelgenerationinhumancellsmiceandrats AT bartelsangela ercas12acrisprmad7formodelgenerationinhumancellsmiceandrats AT vanbrabantsmithanja ercas12acrisprmad7formodelgenerationinhumancellsmiceandrats AT lowechrise ercas12acrisprmad7formodelgenerationinhumancellsmiceandrats AT forbeskevinp ercas12acrisprmad7formodelgenerationinhumancellsmiceandrats |