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利用瞬时转录激活样效应核酸酶进行无基因马铃薯基因组编辑,并通过感染促进再生基因表达。

Integrated gene-free potato genome editing using transient transcription activator-like effector nucleases and regeneration-promoting gene expression by infection.

作者信息

Umemoto Naoyuki, Yasumoto Shuhei, Yamazaki Muneo, Asano Kenji, Akai Kotaro, Lee Hyoung Jae, Akiyama Ryota, Mizutani Masaharu, Nagira Yozo, Saito Kazuki, Muranaka Toshiya

机构信息

RIKEN Center for Sustainable Resource Science, Kanagawa 230-0045, Japan.

Graduate School of Engineering, Osaka University, Osaka 565-0871, Japan.

出版信息

Plant Biotechnol (Tokyo). 2023 Sep 25;40(3):211-218. doi: 10.5511/plantbiotechnology.23.0530a.

DOI:10.5511/plantbiotechnology.23.0530a
PMID:38420569
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10901161/
Abstract

Genome editing is highly useful for crop improvement. The method of expressing genome-editing enzymes using a transient expression system in , called agrobacterial mutagenesis, is a shortcut used in genome-editing technology to improve elite varieties of vegetatively propagated crops, including potato. However, with this method, edited individuals cannot be selected. The transient expression of regeneration-promoting genes can result in shoot regeneration from plantlets, while the constitutive expression of most regeneration-promoting genes does not result in normally regenerated shoots. Here, we report that we could obtain genome-edited potatoes by positive selection. These regenerated shoots were obtained via a method that combined a regeneration-promoting gene with the transient expression of a genome-editing enzyme gene. Moreover, we confirmed that the genome-edited potatoes obtained using this method did not contain the sequence of the binary vector used in . Our data have been submitted to the Japanese regulatory authority, the Ministry of Education, Culture, Sports, Science and Technology (MEXT), and we are in the process of conducting field tests for further research on these potatoes. Our work presents a powerful method for regarding regeneration and acquisition of genome-edited crops through transient expression of regeneration-promoting gene.

摘要

基因组编辑对作物改良非常有用。在植物中使用瞬时表达系统来表达基因组编辑酶的方法,即农杆菌诱变,是基因组编辑技术中用于改良包括马铃薯在内的无性繁殖作物优良品种的一条捷径。然而,用这种方法无法筛选出经过编辑的个体。促进再生的基因的瞬时表达可使植株再生出芽,而大多数促进再生的基因的组成型表达并不会产生正常再生的芽。在此,我们报告通过正向选择能够获得基因组编辑的马铃薯。这些再生芽是通过将促进再生的基因与基因组编辑酶基因的瞬时表达相结合的方法获得的。此外,我们证实使用这种方法获得的基因组编辑马铃薯不包含所用二元载体的序列。我们的数据已提交给日本监管机构文部科学省(MEXT),并且我们正在对这些马铃薯进行田间试验以开展进一步研究。我们的工作提出了一种通过促进再生基因的瞬时表达来实现基因组编辑作物再生和获得编辑作物的强大方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dee/10901161/decc547cc2bb/plantbiotechnology-40-3-23.0530a-figure04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dee/10901161/95083b714f48/plantbiotechnology-40-3-23.0530a-figure01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dee/10901161/8d0b6bfe5f54/plantbiotechnology-40-3-23.0530a-figure02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dee/10901161/e418ebf40329/plantbiotechnology-40-3-23.0530a-figure03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dee/10901161/decc547cc2bb/plantbiotechnology-40-3-23.0530a-figure04.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dee/10901161/95083b714f48/plantbiotechnology-40-3-23.0530a-figure01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dee/10901161/8d0b6bfe5f54/plantbiotechnology-40-3-23.0530a-figure02.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dee/10901161/e418ebf40329/plantbiotechnology-40-3-23.0530a-figure03.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5dee/10901161/decc547cc2bb/plantbiotechnology-40-3-23.0530a-figure04.jpg

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Preface to the special issue "Current Status and Future Prospects for the Development of Crop Varieties and Breeding Materials Using Genome Editing Technology".
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