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CRISPR/Cas9-mediated targeted mutagenesis of GmSPL9 genes alters plant architecture in soybean

BACKGROUND: The plant architecture has significant effects on grain yield of various crops, including soybean (Glycine max), but the knowledge on optimization of plant architecture in order to increase yield potential is still limited. Recently, CRISPR/Cas9 system has revolutionized genome editing,...

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Autores principales: Bao, Aili, Chen, Haifeng, Chen, Limiao, Chen, Shuilian, Hao, Qingnan, Guo, Wei, Qiu, Dezhen, Shan, Zhihui, Yang, Zhonglu, Yuan, Songli, Zhang, Chanjuan, Zhang, Xiaojuan, Liu, Baohui, Kong, Fanjiang, Li, Xia, Zhou, Xinan, Tran, Lam-Son Phan, Cao, Dong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454688/
https://www.ncbi.nlm.nih.gov/pubmed/30961525
http://dx.doi.org/10.1186/s12870-019-1746-6
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author Bao, Aili
Chen, Haifeng
Chen, Limiao
Chen, Shuilian
Hao, Qingnan
Guo, Wei
Qiu, Dezhen
Shan, Zhihui
Yang, Zhonglu
Yuan, Songli
Zhang, Chanjuan
Zhang, Xiaojuan
Liu, Baohui
Kong, Fanjiang
Li, Xia
Zhou, Xinan
Tran, Lam-Son Phan
Cao, Dong
author_facet Bao, Aili
Chen, Haifeng
Chen, Limiao
Chen, Shuilian
Hao, Qingnan
Guo, Wei
Qiu, Dezhen
Shan, Zhihui
Yang, Zhonglu
Yuan, Songli
Zhang, Chanjuan
Zhang, Xiaojuan
Liu, Baohui
Kong, Fanjiang
Li, Xia
Zhou, Xinan
Tran, Lam-Son Phan
Cao, Dong
author_sort Bao, Aili
collection PubMed
description BACKGROUND: The plant architecture has significant effects on grain yield of various crops, including soybean (Glycine max), but the knowledge on optimization of plant architecture in order to increase yield potential is still limited. Recently, CRISPR/Cas9 system has revolutionized genome editing, and has been widely utilized to edit the genomes of a diverse range of crop plants. RESULTS: In the present study, we employed the CRISPR/Cas9 system to mutate four genes encoding SQUAMOSA PROMOTER BINDING PROTEIN-LIKE (SPL) transcription factors of the SPL9 family in soybean. These four GmSPL9 genes are negatively regulated by GmmiR156b, a target for the improvement of soybean plant architecture and yields. The soybean Williams 82 was transformed with the binary CRISPR/Cas9 plasmid, assembled with four sgRNA expression cassettes driven by the Arabidopsis thaliana U3 or U6 promoter, targeting different sites of these four SPL9 genes via Agrobacterium tumefaciens-mediated transformation. A 1-bp deletion was detected in one target site of the GmSPL9a and one target site of the GmSPL9b, respectively, by DNA sequencing analysis of two T0-generation plants. T2-generation spl9a and spl9b homozygous single mutants exhibited no obvious phenotype changes; but the T2 double homozygous mutant spl9a/spl9b possessed shorter plastochron length. In T4 generation, higher-order mutant plants carrying various combinations of mutations showed increased node number on the main stem and branch number, consequently increased total node number per plants at different levels. In addition, the expression levels of the examined GmSPL9 genes were higher in the spl9b-1 single mutant than wild-type plants, which might suggest a feedback regulation on the expression of the investigated GmSPL9 genes in soybean. CONCLUSIONS: Our results showed that CRISPR/Cas9-mediated targeted mutagenesis of four GmSPL9 genes in different combinations altered plant architecture in soybean. The findings demonstrated that GmSPL9a, GmSPL9b, GmSPL9c and GmSPL9 function as redundant transcription factors in regulating plant architecture in soybean. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-019-1746-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-64546882019-04-19 CRISPR/Cas9-mediated targeted mutagenesis of GmSPL9 genes alters plant architecture in soybean Bao, Aili Chen, Haifeng Chen, Limiao Chen, Shuilian Hao, Qingnan Guo, Wei Qiu, Dezhen Shan, Zhihui Yang, Zhonglu Yuan, Songli Zhang, Chanjuan Zhang, Xiaojuan Liu, Baohui Kong, Fanjiang Li, Xia Zhou, Xinan Tran, Lam-Son Phan Cao, Dong BMC Plant Biol Research Article BACKGROUND: The plant architecture has significant effects on grain yield of various crops, including soybean (Glycine max), but the knowledge on optimization of plant architecture in order to increase yield potential is still limited. Recently, CRISPR/Cas9 system has revolutionized genome editing, and has been widely utilized to edit the genomes of a diverse range of crop plants. RESULTS: In the present study, we employed the CRISPR/Cas9 system to mutate four genes encoding SQUAMOSA PROMOTER BINDING PROTEIN-LIKE (SPL) transcription factors of the SPL9 family in soybean. These four GmSPL9 genes are negatively regulated by GmmiR156b, a target for the improvement of soybean plant architecture and yields. The soybean Williams 82 was transformed with the binary CRISPR/Cas9 plasmid, assembled with four sgRNA expression cassettes driven by the Arabidopsis thaliana U3 or U6 promoter, targeting different sites of these four SPL9 genes via Agrobacterium tumefaciens-mediated transformation. A 1-bp deletion was detected in one target site of the GmSPL9a and one target site of the GmSPL9b, respectively, by DNA sequencing analysis of two T0-generation plants. T2-generation spl9a and spl9b homozygous single mutants exhibited no obvious phenotype changes; but the T2 double homozygous mutant spl9a/spl9b possessed shorter plastochron length. In T4 generation, higher-order mutant plants carrying various combinations of mutations showed increased node number on the main stem and branch number, consequently increased total node number per plants at different levels. In addition, the expression levels of the examined GmSPL9 genes were higher in the spl9b-1 single mutant than wild-type plants, which might suggest a feedback regulation on the expression of the investigated GmSPL9 genes in soybean. CONCLUSIONS: Our results showed that CRISPR/Cas9-mediated targeted mutagenesis of four GmSPL9 genes in different combinations altered plant architecture in soybean. The findings demonstrated that GmSPL9a, GmSPL9b, GmSPL9c and GmSPL9 function as redundant transcription factors in regulating plant architecture in soybean. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12870-019-1746-6) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-08 /pmc/articles/PMC6454688/ /pubmed/30961525 http://dx.doi.org/10.1186/s12870-019-1746-6 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
Bao, Aili
Chen, Haifeng
Chen, Limiao
Chen, Shuilian
Hao, Qingnan
Guo, Wei
Qiu, Dezhen
Shan, Zhihui
Yang, Zhonglu
Yuan, Songli
Zhang, Chanjuan
Zhang, Xiaojuan
Liu, Baohui
Kong, Fanjiang
Li, Xia
Zhou, Xinan
Tran, Lam-Son Phan
Cao, Dong
CRISPR/Cas9-mediated targeted mutagenesis of GmSPL9 genes alters plant architecture in soybean
title CRISPR/Cas9-mediated targeted mutagenesis of GmSPL9 genes alters plant architecture in soybean
title_full CRISPR/Cas9-mediated targeted mutagenesis of GmSPL9 genes alters plant architecture in soybean
title_fullStr CRISPR/Cas9-mediated targeted mutagenesis of GmSPL9 genes alters plant architecture in soybean
title_full_unstemmed CRISPR/Cas9-mediated targeted mutagenesis of GmSPL9 genes alters plant architecture in soybean
title_short CRISPR/Cas9-mediated targeted mutagenesis of GmSPL9 genes alters plant architecture in soybean
title_sort crispr/cas9-mediated targeted mutagenesis of gmspl9 genes alters plant architecture in soybean
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6454688/
https://www.ncbi.nlm.nih.gov/pubmed/30961525
http://dx.doi.org/10.1186/s12870-019-1746-6
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