Cargando…

Enhanced rice salinity tolerance via CRISPR/Cas9-targeted mutagenesis of the OsRR22 gene

Salinity is one of the most important abiotic stress affecting the world rice production. The cultivation of salinity-tolerant cultivars is the most cost-effective and environmentally friendly approach for salinity control. In recent years, CRISPR/Cas9 systems have been widely used for target-site g...

Descripción completa

Detalles Bibliográficos
Autores principales: Zhang, Anning, Liu, Yi, Wang, Feiming, Li, Tianfei, Chen, Zhihao, Kong, Deyan, Bi, Junguo, Zhang, Fenyun, Luo, Xingxing, Wang, Jiahong, Tang, Jinjuan, Yu, Xinqiao, Liu, Guolan, Luo, Lijun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7413041/
https://www.ncbi.nlm.nih.gov/pubmed/32803201
http://dx.doi.org/10.1007/s11032-019-0954-y
_version_ 1783568727279665152
author Zhang, Anning
Liu, Yi
Wang, Feiming
Li, Tianfei
Chen, Zhihao
Kong, Deyan
Bi, Junguo
Zhang, Fenyun
Luo, Xingxing
Wang, Jiahong
Tang, Jinjuan
Yu, Xinqiao
Liu, Guolan
Luo, Lijun
author_facet Zhang, Anning
Liu, Yi
Wang, Feiming
Li, Tianfei
Chen, Zhihao
Kong, Deyan
Bi, Junguo
Zhang, Fenyun
Luo, Xingxing
Wang, Jiahong
Tang, Jinjuan
Yu, Xinqiao
Liu, Guolan
Luo, Lijun
author_sort Zhang, Anning
collection PubMed
description Salinity is one of the most important abiotic stress affecting the world rice production. The cultivation of salinity-tolerant cultivars is the most cost-effective and environmentally friendly approach for salinity control. In recent years, CRISPR/Cas9 systems have been widely used for target-site genome editing; however, their application for the improvement of elite rice cultivars has rarely been reported. Here, we report the improvement of the rice salinity tolerance by engineering a Cas9-OsRR22-gRNA expressing vector, targeting the OsRR22 gene in rice. Nine mutant plants were identified from 14 T(0) transgenic plants. Sequencing showed that these plants had six mutation types at the target site, all of which were successfully transmitted to the next generations. Mutant plants without transferred DNA (T-DNA) were obtained via segregation in the T1 generations. Two T2 homozygous mutant lines were further examined for their salinity tolerance and agronomic traits. The results showed that, at the seedling stage, the salinity tolerance of T2 homozygous mutant lines was significantly enhanced compared to wild-type plants. Furthermore, no significantly different agronomic traits were found between T2 homozygous mutant lines and wild-type plants. Our results indicate CRISPR/ Cas9 as a useful approach to enhance the salinity tolerance of rice.
format Online
Article
Text
id pubmed-7413041
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Springer
record_format MEDLINE/PubMed
spelling pubmed-74130412020-08-13 Enhanced rice salinity tolerance via CRISPR/Cas9-targeted mutagenesis of the OsRR22 gene Zhang, Anning Liu, Yi Wang, Feiming Li, Tianfei Chen, Zhihao Kong, Deyan Bi, Junguo Zhang, Fenyun Luo, Xingxing Wang, Jiahong Tang, Jinjuan Yu, Xinqiao Liu, Guolan Luo, Lijun Mol Breed Article Salinity is one of the most important abiotic stress affecting the world rice production. The cultivation of salinity-tolerant cultivars is the most cost-effective and environmentally friendly approach for salinity control. In recent years, CRISPR/Cas9 systems have been widely used for target-site genome editing; however, their application for the improvement of elite rice cultivars has rarely been reported. Here, we report the improvement of the rice salinity tolerance by engineering a Cas9-OsRR22-gRNA expressing vector, targeting the OsRR22 gene in rice. Nine mutant plants were identified from 14 T(0) transgenic plants. Sequencing showed that these plants had six mutation types at the target site, all of which were successfully transmitted to the next generations. Mutant plants without transferred DNA (T-DNA) were obtained via segregation in the T1 generations. Two T2 homozygous mutant lines were further examined for their salinity tolerance and agronomic traits. The results showed that, at the seedling stage, the salinity tolerance of T2 homozygous mutant lines was significantly enhanced compared to wild-type plants. Furthermore, no significantly different agronomic traits were found between T2 homozygous mutant lines and wild-type plants. Our results indicate CRISPR/ Cas9 as a useful approach to enhance the salinity tolerance of rice. Springer 2019-03-09 2019 /pmc/articles/PMC7413041/ /pubmed/32803201 http://dx.doi.org/10.1007/s11032-019-0954-y Text en © The Author(s) 2019 http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Zhang, Anning
Liu, Yi
Wang, Feiming
Li, Tianfei
Chen, Zhihao
Kong, Deyan
Bi, Junguo
Zhang, Fenyun
Luo, Xingxing
Wang, Jiahong
Tang, Jinjuan
Yu, Xinqiao
Liu, Guolan
Luo, Lijun
Enhanced rice salinity tolerance via CRISPR/Cas9-targeted mutagenesis of the OsRR22 gene
title Enhanced rice salinity tolerance via CRISPR/Cas9-targeted mutagenesis of the OsRR22 gene
title_full Enhanced rice salinity tolerance via CRISPR/Cas9-targeted mutagenesis of the OsRR22 gene
title_fullStr Enhanced rice salinity tolerance via CRISPR/Cas9-targeted mutagenesis of the OsRR22 gene
title_full_unstemmed Enhanced rice salinity tolerance via CRISPR/Cas9-targeted mutagenesis of the OsRR22 gene
title_short Enhanced rice salinity tolerance via CRISPR/Cas9-targeted mutagenesis of the OsRR22 gene
title_sort enhanced rice salinity tolerance via crispr/cas9-targeted mutagenesis of the osrr22 gene
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7413041/
https://www.ncbi.nlm.nih.gov/pubmed/32803201
http://dx.doi.org/10.1007/s11032-019-0954-y
work_keys_str_mv AT zhanganning enhancedricesalinitytoleranceviacrisprcas9targetedmutagenesisoftheosrr22gene
AT liuyi enhancedricesalinitytoleranceviacrisprcas9targetedmutagenesisoftheosrr22gene
AT wangfeiming enhancedricesalinitytoleranceviacrisprcas9targetedmutagenesisoftheosrr22gene
AT litianfei enhancedricesalinitytoleranceviacrisprcas9targetedmutagenesisoftheosrr22gene
AT chenzhihao enhancedricesalinitytoleranceviacrisprcas9targetedmutagenesisoftheosrr22gene
AT kongdeyan enhancedricesalinitytoleranceviacrisprcas9targetedmutagenesisoftheosrr22gene
AT bijunguo enhancedricesalinitytoleranceviacrisprcas9targetedmutagenesisoftheosrr22gene
AT zhangfenyun enhancedricesalinitytoleranceviacrisprcas9targetedmutagenesisoftheosrr22gene
AT luoxingxing enhancedricesalinitytoleranceviacrisprcas9targetedmutagenesisoftheosrr22gene
AT wangjiahong enhancedricesalinitytoleranceviacrisprcas9targetedmutagenesisoftheosrr22gene
AT tangjinjuan enhancedricesalinitytoleranceviacrisprcas9targetedmutagenesisoftheosrr22gene
AT yuxinqiao enhancedricesalinitytoleranceviacrisprcas9targetedmutagenesisoftheosrr22gene
AT liuguolan enhancedricesalinitytoleranceviacrisprcas9targetedmutagenesisoftheosrr22gene
AT luolijun enhancedricesalinitytoleranceviacrisprcas9targetedmutagenesisoftheosrr22gene