CRISPR/Cas9-based gene activation and base editing in Populus

被引:8
|
作者
Yao, Tao [1 ,2 ]
Yuan, Guoliang [1 ,2 ,3 ]
Lu, Haiwei [1 ,4 ]
Liu, Yang [1 ]
Zhang, Jin [1 ,5 ]
Tuskan, Gerald A. [1 ,2 ]
Muchero, Wellington [1 ,2 ]
Chen, Jin-Gui [1 ,2 ]
Yang, Xiaohan [1 ,2 ]
机构
[1] Oak Ridge Natl Lab, Biosci Div, Oak Ridge, TN 37831 USA
[2] Oak Ridge Natl Lab, Ctr Bioenergy Innovat, Oak Ridge, TN 37831 USA
[3] Pacific Northwest Natl Lab, Chem & Biol Proc Dev Grp, 902 Battelle Blvd, Richland, WA 99352 USA
[4] Cent Community Coll Hastings, Dept Acad Educ, Hastings, NE 68901 USA
[5] Zhejiang A&F Univ, Coll Forestry & Biotechnol, State Key Lab Subtrop Silviculture, Hangzhou 311300, Peoples R China
关键词
TARGETED MUTAGENESIS; GENOME; EXPRESSION; OVEREXPRESSION; SYSTEM;
D O I
10.1093/hr/uhad085
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The genus Populus has long been used for environmental, agroforestry and industrial applications worldwide. Today Populus is also recognized as a desirable crop for biofuel production and a model tree for physiological and ecological research. As such, various modern biotechnologies, including CRISPR/Cas9-based techniques, have been actively applied to Populus for genetic and genomic improvements for traits such as increased growth rate and tailored lignin composition. However, CRISPR/Cas9 has been primarily used as the active Cas9 form to create knockouts in the hybrid poplar clone "717-1B4" (P. tremula x P. alba clone INRA 717-1B4). Alternative CRISPR/Cas9-based technologies, e.g. those involving modified Cas9 for gene activation and base editing, have not been evaluated in most Populus species for their efficacy. Here we employed a deactivated Cas9 (dCas9)-based CRISPR activation (CRISPRa) technique to fine-tune the expression of two target genes, TPX2 and LecRLK-G which play important roles in plant growth and defense response, in hybrid poplar clone "717-1B4" and poplar clone "WV94" (P. deltoides "WV94"), respectively. We observed that CRISPRa resulted in 1.2-fold to 7.0-fold increase in target gene expression through transient expression in protoplasts and Agrobacterium-mediated stable transformation, demonstrating the effectiveness of dCas9-based CRISPRa system in Populus. In addition, we applied Cas9 nickase (nCas9)-based cytosine base editor (CBE) to precisely introduce premature stop codons via C-to-T conversion, with an efficiency of 13%-14%, in the target gene PLATZ which encodes a transcription factor involved in plant fungal pathogen response in hybrid poplar clone "717-1B4". Overall, we showcase the successful application of CRISPR/Cas-based technologies in gene expression regulation and precise gene engineering in two Populus species, facilitating the adoption of emerging genome editing tools in woody species.
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收藏
页数:9
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