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Generation of a multiplex mutagenesis population via pooled CRISPR‐Cas9 in soya bean
The output of genetic mutant screenings in soya bean [Glycine max (L.) Merr.] has been limited by its paleopolypoid genome. CRISPR‐Cas9 can generate multiplex mutants in crops with complex genomes. Nevertheless, the transformation efficiency of soya bean remains low and, hence, remains the major obs...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004907/ https://www.ncbi.nlm.nih.gov/pubmed/31452351 http://dx.doi.org/10.1111/pbi.13239 |
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author | Bai, Mengyan Yuan, Juehui Kuang, Huaqin Gong, Pingping Li, Suning Zhang, Zhihui Liu, Bo Sun, Jiafeng Yang, Maoxiang Yang, Lan Wang, Dong Song, Shikui Guan, Yuefeng |
author_facet | Bai, Mengyan Yuan, Juehui Kuang, Huaqin Gong, Pingping Li, Suning Zhang, Zhihui Liu, Bo Sun, Jiafeng Yang, Maoxiang Yang, Lan Wang, Dong Song, Shikui Guan, Yuefeng |
author_sort | Bai, Mengyan |
collection | PubMed |
description | The output of genetic mutant screenings in soya bean [Glycine max (L.) Merr.] has been limited by its paleopolypoid genome. CRISPR‐Cas9 can generate multiplex mutants in crops with complex genomes. Nevertheless, the transformation efficiency of soya bean remains low and, hence, remains the major obstacle in the application of CRISPR‐Cas9 as a mutant screening tool. Here, we report a pooled CRISPR‐Cas9 platform to generate soya bean multiplex mutagenesis populations. We optimized the key steps in the screening protocol, including vector construction, sgRNA assessment, pooled transformation, sgRNA identification and gene editing verification. We constructed 70 CRISPR‐Cas9 vectors to target 102 candidate genes and their paralogs which were subjected to pooled transformation in 16 batches. A population consisting of 407 T0 lines was obtained containing all sgRNAs at an average mutagenesis frequency of 59.2%, including 35.6% lines carrying multiplex mutations. The mutation frequency in the T1 progeny could be increased further despite obtaining a transgenic chimera. In this population, we characterized gmric1/gmric2 double mutants with increased nodule numbers and gmrdn1‐1/1‐2/1‐3 triple mutant lines with decreased nodulation. Our study provides an advanced strategy for the generation of a targeted multiplex mutant population to overcome the gene redundancy problem in soya bean as well as in other major crops. |
format | Online Article Text |
id | pubmed-7004907 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70049072020-02-13 Generation of a multiplex mutagenesis population via pooled CRISPR‐Cas9 in soya bean Bai, Mengyan Yuan, Juehui Kuang, Huaqin Gong, Pingping Li, Suning Zhang, Zhihui Liu, Bo Sun, Jiafeng Yang, Maoxiang Yang, Lan Wang, Dong Song, Shikui Guan, Yuefeng Plant Biotechnol J Research Articles The output of genetic mutant screenings in soya bean [Glycine max (L.) Merr.] has been limited by its paleopolypoid genome. CRISPR‐Cas9 can generate multiplex mutants in crops with complex genomes. Nevertheless, the transformation efficiency of soya bean remains low and, hence, remains the major obstacle in the application of CRISPR‐Cas9 as a mutant screening tool. Here, we report a pooled CRISPR‐Cas9 platform to generate soya bean multiplex mutagenesis populations. We optimized the key steps in the screening protocol, including vector construction, sgRNA assessment, pooled transformation, sgRNA identification and gene editing verification. We constructed 70 CRISPR‐Cas9 vectors to target 102 candidate genes and their paralogs which were subjected to pooled transformation in 16 batches. A population consisting of 407 T0 lines was obtained containing all sgRNAs at an average mutagenesis frequency of 59.2%, including 35.6% lines carrying multiplex mutations. The mutation frequency in the T1 progeny could be increased further despite obtaining a transgenic chimera. In this population, we characterized gmric1/gmric2 double mutants with increased nodule numbers and gmrdn1‐1/1‐2/1‐3 triple mutant lines with decreased nodulation. Our study provides an advanced strategy for the generation of a targeted multiplex mutant population to overcome the gene redundancy problem in soya bean as well as in other major crops. John Wiley and Sons Inc. 2019-09-09 2020-03 /pmc/articles/PMC7004907/ /pubmed/31452351 http://dx.doi.org/10.1111/pbi.13239 Text en © 2019 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Research Articles Bai, Mengyan Yuan, Juehui Kuang, Huaqin Gong, Pingping Li, Suning Zhang, Zhihui Liu, Bo Sun, Jiafeng Yang, Maoxiang Yang, Lan Wang, Dong Song, Shikui Guan, Yuefeng Generation of a multiplex mutagenesis population via pooled CRISPR‐Cas9 in soya bean |
title | Generation of a multiplex mutagenesis population via pooled CRISPR‐Cas9 in soya bean |
title_full | Generation of a multiplex mutagenesis population via pooled CRISPR‐Cas9 in soya bean |
title_fullStr | Generation of a multiplex mutagenesis population via pooled CRISPR‐Cas9 in soya bean |
title_full_unstemmed | Generation of a multiplex mutagenesis population via pooled CRISPR‐Cas9 in soya bean |
title_short | Generation of a multiplex mutagenesis population via pooled CRISPR‐Cas9 in soya bean |
title_sort | generation of a multiplex mutagenesis population via pooled crispr‐cas9 in soya bean |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7004907/ https://www.ncbi.nlm.nih.gov/pubmed/31452351 http://dx.doi.org/10.1111/pbi.13239 |
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