Application of CRISPR/Cas9 genome editing system for molecular breeding of orchids

Q4 Environmental Science
E. Semiarti, S. Nopitasari, Y. Setiawati, M. D. Lawrie, A. Purwantoro, J. Widada, Y. Yoshioka, S. Matsumoto, K. Ninomiya, Yuuki Asano
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引用次数: 7

Abstract

Orchid is an important ornamental plant in Indonesia due to their natural beauty of flowers. In the tropical forest, orchids are being acquired for trading and commercial market. Thus, the effort is required to proliferate orchid in large quantities for conservation and improve the floral variation for plant breeding. The purpose of this study is to develop a firmed methodology of molecular breeding of orchids using CRISPR/Cas9 KO system. The plant material used was Phalaenopsis amabilis protocorms growth on NP medium+pepton (2 g/L). Protocorm were submerged in the culture of Agrobacterium tumefaciens that Ti‐plasmid had been filled with a T‐DNA construct of a pRGEB32 vector harboring sgRNA with PDS3 sequence. Detection for transformants was confirmed by PCR using HPT primers (545 bp), Cas9 primers (402 bp), PDS primers (280 bp) and trnL‐F (1200 bp) as an internal control. The results showed that 0.96% PDS transformants were obtained from PDS3T2 lines. Several transformant showed pale leaf color compared to non‐transformant plants. This study suggests that the target gene has successfully edited by CRISPR/Cas9 system and could be applied for that functional gene editing in orchids.
CRISPR/Cas9基因组编辑系统在兰花分子育种中的应用
兰花是印度尼西亚一种重要的观赏植物,因为它的花很自然。在热带森林中,兰花被收购用于贸易和商业市场。因此,需要努力大量繁殖兰花以进行保护,并改善植物育种的花变异。本研究的目的是利用CRISPR/Cas9-KO系统开发一种确定的兰花分子育种方法。所用的植物材料是在NP培养基+pepton(2g/L)上生长的蝴蝶兰原球茎。将原球茎浸没在根癌农杆菌的培养物中,其中Ti‐质粒填充有pRGEB32载体的T‐DNA构建体,该载体携带具有PDS3序列的sgRNA。使用HPT引物(545 bp)、Cas9引物(402 bp)、PDS引物(280 bp)和trnL‐F(1200 bp)作为内部对照,通过PCR确认对转化体的检测。结果表明,从PDS3T2系中获得了0.96%的PDS转化体。与非转化植株相比,一些转化植株的叶片颜色较浅。本研究表明,该靶基因已被CRISPR/Cas9系统成功编辑,可用于兰花的功能性基因编辑。
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来源期刊
Indonesian Journal of Biotechnology
Indonesian Journal of Biotechnology Environmental Science-Environmental Science (miscellaneous)
CiteScore
1.00
自引率
0.00%
发文量
20
审稿时长
12 weeks
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