High efficiency of targeted mutagenesis in arabidopsis via meiotic promoter-driven expression of Cas9 endonuclease
KAUST DepartmentBiological and Environmental Sciences and Engineering (BESE) Division
Desert Agriculture Initiative
Laboratory for Genome Engineering
Plant Science Program
Online Publication Date2016-05-28
Print Publication Date2016-07
Permanent link to this recordhttp://hdl.handle.net/10754/621397
MetadataShow full item record
AbstractKey message: The use of a meiosis I-specific promoter increased the efficiency of targeted mutagenesis and will facilitate the manipulation of homologous recombination. Abstract: The CRISPR/Cas9 system has been harnessed for targeted engineering of eukaryotic genomes, including plants; however, CRISPR/Cas9 efficiency varies considerably in different plant tissues and species. In Arabidopsis, the generation of homozygous or bi-allelic mutants in the first (T1) generation is inefficient. Here, we used specific promoters to drive the expression of Cas9 during meiosis to maximize the efficiency of recovering heritable mutants in T1 plants. Our data reveal that the use of a promoter active in meiosis I resulted in high-efficiency (28 %) recovery of targeted mutants in the T1 generation. Moreover, this method enabled efficient simultaneous targeting of three genes for mutagenesis. Taken together, our results show that the use of meiosis-specific promoters will improve methods for functional genomic analysis and studying the molecular underpinnings of homologous recombination. © 2016, Springer-Verlag Berlin Heidelberg.
CitationEid A, Ali Z, Mahfouz MM (2016) High efficiency of targeted mutagenesis in arabidopsis via meiotic promoter-driven expression of Cas9 endonuclease. Plant Cell Reports 35: 1555–1558. Available: http://dx.doi.org/10.1007/s00299-016-2000-4.
SponsorsWe thank Qi-Jun Chen, State Key Laboratory of Plant Physiology and Biochemistry China Agricultural University, for providing the pHEE2A-TRI vector backbone. We thank members of the Laboratory for Genome Engineering at King Abdullah University of Science and Technology for helpful discussions and comments. The study was supported by the King Abdullah University of Science and Technology.
JournalPlant Cell Reports
- Site-directed mutagenesis in Arabidopsis thaliana using dividing tissue-targeted RGEN of the CRISPR/Cas system to generate heritable null alleles.
- Authors: Hyun Y, Kim J, Cho SW, Choi Y, Kim JS, Coupland G
- Issue date: 2015 Jan
- A multiplex CRISPR/Cas9 platform for fast and efficient editing of multiple genes in Arabidopsis.
- Authors: Zhang Z, Mao Y, Ha S, Liu W, Botella JR, Zhu JK
- Issue date: 2016 Jul
- A Highly Efficient Cell Division-Specific CRISPR/Cas9 System Generates Homozygous Mutants for Multiple Genes in <i>Arabidopsis</i>.
- Authors: Feng Z, Zhang Z, Hua K, Gao X, Mao Y, Botella JR, Zhu JK
- Issue date: 2018 Dec 7
- Highly efficient heritable plant genome engineering using Cas9 orthologues from Streptococcus thermophilus and Staphylococcus aureus.
- Authors: Steinert J, Schiml S, Fauser F, Puchta H
- Issue date: 2015 Dec
- Pea early-browning virus-mediated genome editing via the CRISPR/Cas9 system in Nicotiana benthamiana and Arabidopsis.
- Authors: Ali Z, Eid A, Ali S, Mahfouz MM
- Issue date: 2018 Jan 15