Cargando…

CRISPR-Cas9 mediated targeted disruption of FAD2–2 microsomal omega-6 desaturase in soybean (Glycine max.L)

BACKGROUND: Recent innovation in the field of genome engineering encompasses numerous levels of plant genome engineering which attract the substantial excitement of plant biologist worldwide. RNA-guided CRISPR Cas9 system has appeared a promising tool in site-directed mutagenesis due to its innovati...

Descripción completa

Detalles Bibliográficos
Autores principales: al Amin, Noor, Ahmad, Naveed, Wu, Nan, Pu, Xiumin, Ma, Tong, Du, Yeyao, Bo, Xiaoxue, Wang, Nan, Sharif, Rahat, Wang, Piwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350355/
https://www.ncbi.nlm.nih.gov/pubmed/30691438
http://dx.doi.org/10.1186/s12896-019-0501-2
_version_ 1783390437303648256
author al Amin, Noor
Ahmad, Naveed
Wu, Nan
Pu, Xiumin
Ma, Tong
Du, Yeyao
Bo, Xiaoxue
Wang, Nan
Sharif, Rahat
Wang, Piwu
author_facet al Amin, Noor
Ahmad, Naveed
Wu, Nan
Pu, Xiumin
Ma, Tong
Du, Yeyao
Bo, Xiaoxue
Wang, Nan
Sharif, Rahat
Wang, Piwu
author_sort al Amin, Noor
collection PubMed
description BACKGROUND: Recent innovation in the field of genome engineering encompasses numerous levels of plant genome engineering which attract the substantial excitement of plant biologist worldwide. RNA-guided CRISPR Cas9 system has appeared a promising tool in site-directed mutagenesis due to its innovative utilization in different branches of biology. CRISPR-Cas9 nuclease system have supersedes all previously existed strategies and their associated pitfalls encountered with site-specific mutagenesis. RESULTS: Here we demonstrated an efficient sequence specific integration/mutation of FAD2–2 gene in soybean using CRISPR-Cas9 nuclease system. A single guided RNA sequence was designed with the help of a number of bioinformatics tools aimed to target distinct sites of FAD2–2 loci in soybean. The binary vector (pCas9-AtU6-sgRNA) has been successfully transformed into soybean cotyledon using Agrobacterium tumafacien. Taken together our findings complies soybean transgenic mutants subjected to targeted mutation were surprisingly detected in our target gene. Furthermore, the detection of Cas9 gene, BAR gene, and NOS terminator were carried out respectively. Southern blot analysis confirmed the stable transformation of Cas9 gene into soybean. Real time expression with qRT-PCR and Sanger sequencing analysis confirmed the efficient CRISPR-Cas9/sgRNA induced mutation within the target sequence of FAD2–2 loci. The integration of FAD2–2 target region in the form of substitution, deletions and insertions were achieved with notably high frequency and rare off-target mutagenesis. CONCLUSION: High frequent mutation efficiency was recorded as 21% out of all transgenic soybean plants subjected to targeted mutagenesis. Furthermore, Near-infrared spectroscopy (NIR) indicates the entire fatty acid profiling obtained from the mutants seeds of soybean. A considerable modulation in oleic acid content up to (65.58%) whereas the least level of linoleic acid is (16.08%) were recorded. Based on these finding CRISPR-Cas9 system can possibly sum up recent development and future challenges in producing agronomically important crops. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12896-019-0501-2) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6350355
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-63503552019-02-04 CRISPR-Cas9 mediated targeted disruption of FAD2–2 microsomal omega-6 desaturase in soybean (Glycine max.L) al Amin, Noor Ahmad, Naveed Wu, Nan Pu, Xiumin Ma, Tong Du, Yeyao Bo, Xiaoxue Wang, Nan Sharif, Rahat Wang, Piwu BMC Biotechnol Research Article BACKGROUND: Recent innovation in the field of genome engineering encompasses numerous levels of plant genome engineering which attract the substantial excitement of plant biologist worldwide. RNA-guided CRISPR Cas9 system has appeared a promising tool in site-directed mutagenesis due to its innovative utilization in different branches of biology. CRISPR-Cas9 nuclease system have supersedes all previously existed strategies and their associated pitfalls encountered with site-specific mutagenesis. RESULTS: Here we demonstrated an efficient sequence specific integration/mutation of FAD2–2 gene in soybean using CRISPR-Cas9 nuclease system. A single guided RNA sequence was designed with the help of a number of bioinformatics tools aimed to target distinct sites of FAD2–2 loci in soybean. The binary vector (pCas9-AtU6-sgRNA) has been successfully transformed into soybean cotyledon using Agrobacterium tumafacien. Taken together our findings complies soybean transgenic mutants subjected to targeted mutation were surprisingly detected in our target gene. Furthermore, the detection of Cas9 gene, BAR gene, and NOS terminator were carried out respectively. Southern blot analysis confirmed the stable transformation of Cas9 gene into soybean. Real time expression with qRT-PCR and Sanger sequencing analysis confirmed the efficient CRISPR-Cas9/sgRNA induced mutation within the target sequence of FAD2–2 loci. The integration of FAD2–2 target region in the form of substitution, deletions and insertions were achieved with notably high frequency and rare off-target mutagenesis. CONCLUSION: High frequent mutation efficiency was recorded as 21% out of all transgenic soybean plants subjected to targeted mutagenesis. Furthermore, Near-infrared spectroscopy (NIR) indicates the entire fatty acid profiling obtained from the mutants seeds of soybean. A considerable modulation in oleic acid content up to (65.58%) whereas the least level of linoleic acid is (16.08%) were recorded. Based on these finding CRISPR-Cas9 system can possibly sum up recent development and future challenges in producing agronomically important crops. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12896-019-0501-2) contains supplementary material, which is available to authorized users. BioMed Central 2019-01-28 /pmc/articles/PMC6350355/ /pubmed/30691438 http://dx.doi.org/10.1186/s12896-019-0501-2 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
al Amin, Noor
Ahmad, Naveed
Wu, Nan
Pu, Xiumin
Ma, Tong
Du, Yeyao
Bo, Xiaoxue
Wang, Nan
Sharif, Rahat
Wang, Piwu
CRISPR-Cas9 mediated targeted disruption of FAD2–2 microsomal omega-6 desaturase in soybean (Glycine max.L)
title CRISPR-Cas9 mediated targeted disruption of FAD2–2 microsomal omega-6 desaturase in soybean (Glycine max.L)
title_full CRISPR-Cas9 mediated targeted disruption of FAD2–2 microsomal omega-6 desaturase in soybean (Glycine max.L)
title_fullStr CRISPR-Cas9 mediated targeted disruption of FAD2–2 microsomal omega-6 desaturase in soybean (Glycine max.L)
title_full_unstemmed CRISPR-Cas9 mediated targeted disruption of FAD2–2 microsomal omega-6 desaturase in soybean (Glycine max.L)
title_short CRISPR-Cas9 mediated targeted disruption of FAD2–2 microsomal omega-6 desaturase in soybean (Glycine max.L)
title_sort crispr-cas9 mediated targeted disruption of fad2–2 microsomal omega-6 desaturase in soybean (glycine max.l)
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350355/
https://www.ncbi.nlm.nih.gov/pubmed/30691438
http://dx.doi.org/10.1186/s12896-019-0501-2
work_keys_str_mv AT alaminnoor crisprcas9mediatedtargeteddisruptionoffad22microsomalomega6desaturaseinsoybeanglycinemaxl
AT ahmadnaveed crisprcas9mediatedtargeteddisruptionoffad22microsomalomega6desaturaseinsoybeanglycinemaxl
AT wunan crisprcas9mediatedtargeteddisruptionoffad22microsomalomega6desaturaseinsoybeanglycinemaxl
AT puxiumin crisprcas9mediatedtargeteddisruptionoffad22microsomalomega6desaturaseinsoybeanglycinemaxl
AT matong crisprcas9mediatedtargeteddisruptionoffad22microsomalomega6desaturaseinsoybeanglycinemaxl
AT duyeyao crisprcas9mediatedtargeteddisruptionoffad22microsomalomega6desaturaseinsoybeanglycinemaxl
AT boxiaoxue crisprcas9mediatedtargeteddisruptionoffad22microsomalomega6desaturaseinsoybeanglycinemaxl
AT wangnan crisprcas9mediatedtargeteddisruptionoffad22microsomalomega6desaturaseinsoybeanglycinemaxl
AT sharifrahat crisprcas9mediatedtargeteddisruptionoffad22microsomalomega6desaturaseinsoybeanglycinemaxl
AT wangpiwu crisprcas9mediatedtargeteddisruptionoffad22microsomalomega6desaturaseinsoybeanglycinemaxl