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Highly efficient Agrobacterium rhizogenes-mediated hairy root transformation for gene editing analysis in cotton
CRIPSR/Cas9 gene editing system is an effective tool for genome modification in plants. Multiple target sites are usually designed and the effective target sites are selected for editing. Upland cotton (Gossypium hirsutum L., hereafter cotton) is allotetraploid and is commonly considered as difficul...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832336/ https://www.ncbi.nlm.nih.gov/pubmed/36643290 http://dx.doi.org/10.3389/fpls.2022.1059404 |
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author | Zhou, Lili Wang, Yali Wang, Peilin Wang, Chunling Wang, Jiamin Wang, Xingfen Cheng, Hongmei |
author_facet | Zhou, Lili Wang, Yali Wang, Peilin Wang, Chunling Wang, Jiamin Wang, Xingfen Cheng, Hongmei |
author_sort | Zhou, Lili |
collection | PubMed |
description | CRIPSR/Cas9 gene editing system is an effective tool for genome modification in plants. Multiple target sites are usually designed and the effective target sites are selected for editing. Upland cotton (Gossypium hirsutum L., hereafter cotton) is allotetraploid and is commonly considered as difficult and inefficient to transform, it is important to select the effective target sites that could result in the ideal transgenic plants with the CRISPR-induced mutations. In this study, Agrobacterium rhizogenes-mediated hairy root method was optimized to detect the feasibility of the target sites designed in cotton phytoene desaturase (GhPDS) gene. A. rhizogenes showed the highest hairy root induction (30%) when the bacteria were cultured until OD(600) reached to 0.8. This procedure was successfully applied to induce hairy roots in the other three cultivars (TM–1, Lumian–21, Zhongmian–49) and the mutations were detected in GhPDS induced by CRISPR/Cas9 system. Different degrees of base deletions at two sgRNAs (sgRNA5 and sgRNA10) designed in GhPDS were detected in R15 hairy roots. Furthermore, we obtained an albino transgenic cotton seeding containing CRISPR/Cas9-induced gene editing mutations in sgRNA10. The hairy root transformation system established in this study is sufficient for selecting sgRNAs in cotton, providing a technical basis for functional genomics research of cotton. |
format | Online Article Text |
id | pubmed-9832336 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98323362023-01-12 Highly efficient Agrobacterium rhizogenes-mediated hairy root transformation for gene editing analysis in cotton Zhou, Lili Wang, Yali Wang, Peilin Wang, Chunling Wang, Jiamin Wang, Xingfen Cheng, Hongmei Front Plant Sci Plant Science CRIPSR/Cas9 gene editing system is an effective tool for genome modification in plants. Multiple target sites are usually designed and the effective target sites are selected for editing. Upland cotton (Gossypium hirsutum L., hereafter cotton) is allotetraploid and is commonly considered as difficult and inefficient to transform, it is important to select the effective target sites that could result in the ideal transgenic plants with the CRISPR-induced mutations. In this study, Agrobacterium rhizogenes-mediated hairy root method was optimized to detect the feasibility of the target sites designed in cotton phytoene desaturase (GhPDS) gene. A. rhizogenes showed the highest hairy root induction (30%) when the bacteria were cultured until OD(600) reached to 0.8. This procedure was successfully applied to induce hairy roots in the other three cultivars (TM–1, Lumian–21, Zhongmian–49) and the mutations were detected in GhPDS induced by CRISPR/Cas9 system. Different degrees of base deletions at two sgRNAs (sgRNA5 and sgRNA10) designed in GhPDS were detected in R15 hairy roots. Furthermore, we obtained an albino transgenic cotton seeding containing CRISPR/Cas9-induced gene editing mutations in sgRNA10. The hairy root transformation system established in this study is sufficient for selecting sgRNAs in cotton, providing a technical basis for functional genomics research of cotton. Frontiers Media S.A. 2022-12-23 /pmc/articles/PMC9832336/ /pubmed/36643290 http://dx.doi.org/10.3389/fpls.2022.1059404 Text en Copyright © 2022 Zhou, Wang, Wang, Wang, Wang, Wang and Cheng https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Plant Science Zhou, Lili Wang, Yali Wang, Peilin Wang, Chunling Wang, Jiamin Wang, Xingfen Cheng, Hongmei Highly efficient Agrobacterium rhizogenes-mediated hairy root transformation for gene editing analysis in cotton |
title | Highly efficient Agrobacterium rhizogenes-mediated hairy root transformation for gene editing analysis in cotton |
title_full | Highly efficient Agrobacterium rhizogenes-mediated hairy root transformation for gene editing analysis in cotton |
title_fullStr | Highly efficient Agrobacterium rhizogenes-mediated hairy root transformation for gene editing analysis in cotton |
title_full_unstemmed | Highly efficient Agrobacterium rhizogenes-mediated hairy root transformation for gene editing analysis in cotton |
title_short | Highly efficient Agrobacterium rhizogenes-mediated hairy root transformation for gene editing analysis in cotton |
title_sort | highly efficient agrobacterium rhizogenes-mediated hairy root transformation for gene editing analysis in cotton |
topic | Plant Science |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9832336/ https://www.ncbi.nlm.nih.gov/pubmed/36643290 http://dx.doi.org/10.3389/fpls.2022.1059404 |
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