| Literature DB >> 29226588 |
Zhiming Yu1, Qiyuan Chen1, Weiwei Chen1, Xian Zhang1, Fengling Mei1, Pengcheng Zhang1, Mei Zhao1, Xiaohong Wang1, Nongnong Shi1, Stephen Jackson2, Yiguo Hong1,2,3.
Abstract
We report that a solo single-guide RNA (sgRNA) seed is capable of guiding Clustered Regularly Interspaced Short Palindromic Repeats (CRISPR)/CRISPR -associated 9 (CRISRP/Cas9) to simultaneously edit multiple genes AtRPL10A, AtRPL10B and AtRPL10C in Arabidopsis. Our results also demonstrate that it is possible to use CRISPR/Cas9 technology to create AtRPL10 triple mutants which otherwise cannot be generated by conventional genetic crossing. Compared to other conventional multiplex CRISPR/Cas systems, a single sgRNA seed has the advantage of reducing off-target gene-editing. Such a gene editing system might be also applicable to modify other homologous genes, or even less-homologous sequences for multiple gene-editing in plants and other organisms.Entities:
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Year: 2018 PMID: 29226588 DOI: 10.1111/jipb.12622
Source DB: PubMed Journal: J Integr Plant Biol ISSN: 1672-9072 Impact factor: 7.061