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Expanding the scope of plant genome engineering with Cas12a orthologs and highly multiplexable editing systems

文献类型: 外文期刊

作者: Zhang, Yingxiao 1 ; Ren, Qiurong 2 ; Tang, Xu 2 ; Liu, Shishi 2 ; Malzahn, Aimee A. 1 ; Zhou, Jianping 2 ; Wang, Jiahe 1 ;

作者机构: 1.Univ Maryland, Dept Plant Sci & Landscape Architecture, College Pk, MD 20742 USA

2.Univ Elect Sci & Technol China, Ctr Informat Biol, Sch Life Sci & Technol, Dept Biotechnol, Chengdu, Peoples R China

3.Hubei Acad Agr Sci, Food Crop Inst, Wuhan, Hubei, Peoples R China

4.Nanjing Agr Univ, Coll Agr, Nanjing, Jiangsu, Peoples R China

5.Univ Maryland, Ctr Bioinformat & Computat Biol, College Pk, MD 20742 USA

6.Univ Maryland, Dept Cell Biol & Mol Genet, College Pk, MD 20742 USA

7.Syngenta, Res Triangle Pk, NC USA

8.Univ Maryland, Inst Biosci & Biotechnol Res, Rockville, MD USA

期刊名称:NATURE COMMUNICATIONS ( 影响因子:12.121; 五年影响因子:13.61 )

ISSN: 2041-1723

年卷期: 2021 年 12 卷 1 期

页码:

收录情况: SCI

摘要: CRISPR-Cas12a is a promising genome editing system for targeting AT-rich genomic regions. Comprehensive genome engineering requires simultaneous targeting of multiple genes at defined locations. Here, to expand the targeting scope of Cas12a, we screen nine Cas12a orthologs that have not been demonstrated in plants, and identify six, ErCas12a, Lb5Cas12a, BsCas12a, Mb2Cas12a, TsCas12a and MbCas12a, that possess high editing activity in rice. Among them, Mb2Cas12a stands out with high editing efficiency and tolerance to low temperature. An engineered Mb2Cas12a-RVRR variant enables editing with more relaxed PAM requirements in rice, yielding two times higher genome coverage than the wild type SpCas9. To enable large-scale genome engineering, we compare 12 multiplexed Cas12a systems and identify a potent system that exhibits nearly 100% biallelic editing efficiency with the ability to target as many as 16 sites in rice. This is the highest level of multiplex edits in plants to date using Cas12a. Two compact single transcript unit CRISPR-Cas12a interference systems are also developed for multi-gene repression in rice and Arabidopsis. This study greatly expands the targeting scope of Cas12a for crop genome engineering. CRISPR-Cas12a is a promising system for targeting AT-rich regions of the genome. Here the authors identify Cas12a orthologs with expanded targeting scope and develop a highly multiplexable editing system in rice.

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