An optimized CRISPRCas9-based gene editing system for efficiently generating homozygous edited plants in rubber tree ( Hevea brasiliensis) )
文献类型: 外文期刊
第一作者: Yang, Xianfeng
作者: Yang, Xianfeng;Lin, Qiufei;Udayabhanu, Jinu;Hua, Yuwei;Dai, Xuemei;Xin, Shichao;Wang, Xiaoyi;Huang, Huasun;Huang, Tiandai;Yang, Xianfeng;Xin, Shichao;Wang, Xiaoyi;Huang, Huasun;Huang, Tiandai;Yang, Xianfeng;Lin, Qiufei;Udayabhanu, Jinu;Dai, Xuemei;Xin, Shichao;Wang, Xiaoyi;Huang, Huasun;Huang, Tiandai
作者机构:
关键词: Rubber tree; CRISPR/Cas9; Genetic transformation; Gene editing; Embryo; Homozygous
期刊名称:INDUSTRIAL CROPS AND PRODUCTS ( 影响因子:6.2; 五年影响因子:6.2 )
ISSN: 0926-6690
年卷期: 2024 年 222 卷
页码:
收录情况: SCI
摘要: Previously, we have realized CRISPR/Cas9-RNP and plasmid-mediated genome editing in the rubber tree protoplast by transient transformation, but it is a challenge to generate editing plants hindered by low stable genetic transformation efficiency. In the present study, we firstly reported genome-edited rubber trees with expected phenotype, related works including demonstrated that 10 mg/L hygromycin is suitable for embryo screening, based on this foundation, CRISPR vector targeting the Phytoene desaturase gene ( HbPDS ) was transformed into embryos, the results showed that more than 90% of T0 edited embryos are chimeric, and the editing efficiency is 3.2%. In order to improve the homozygous embryo ratio, a T0 embryo with 9.8% edited cells was sliced into 33 small pieces for one more cycle embryogenesis to produce T1 generation embryos, it turns out the editing efficiency has been improved to nearly 90%, and 50% of T1 embryos were homozygous. At last, 8 plantlets were regenerated from the 29 T1 generation edited embryos, 4 chimeric and 4 homozygous albino plantlets, respectively. Next-generation sequencing demonstrated that, the threshold for the proportion of edited cells displaying expected albino phenotype is between 70 % and 85 %. Additionally, Tail-PCR' results, combined the different genotypes considered, the four homozygous plantlets can be confirmed as independently derived from different single transformed cells. Overall, this study presents a significant advancement in transgenic and gene editing for rubber trees, will be conducive to gene functional validation and accelerate the molecular breeding process of rubber tree.
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