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Cas12a和MAD7,用于育种的基因组编辑工具。

Cas12a and MAD7, genome editing tools for breeding.

作者信息

Hozumi Shunya, Chen Yi-Chen, Takemoto Tatsuya, Sawatsubashi Shun

机构信息

Setsuro Tech Inc., Fujii Memorial Institute of Medical Sciences, 3-18-15 Kuramoto-cho, Tokushima 770-8503, Japan.

Laboratory for Embryology, Institute for Advanced Medical Sciences, Tokushima University, 3-18-15 Kuramoto-cho, Tokushima 770-8503, Japan.

出版信息

Breed Sci. 2024 Mar;74(1):22-31. doi: 10.1270/jsbbs.23049. Epub 2024 Feb 22.

DOI:10.1270/jsbbs.23049
PMID:39246434
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11375424/
Abstract

Food shortages due to population growth and climate change are expected to occur in the near future as a problem that urgently requires solutions. Conventional breeding techniques, notably crossbreeding and mutation breeding, are known for being inefficient and time-consuming in obtaining seeds and seedlings with desired traits. Thus, there is an urgent need for novel methods for efficient plant breeding. Breeding by genome editing is receiving substantial attention because it can efficiently modify the target gene to obtain desired traits compared with conventional methods. Among the programmable sequence-specific nucleases that have been developed for genome editing, CRISPR-Cas12a and CRISPR-MAD7 nucleases are becoming more broadly adopted for the application of genome editing in grains, vegetables and fruits. Additionally, ST8, an improved variant of MAD7, has been developed to enhance genome editing efficiency and has potential for application to breeding of crops.

摘要

由于人口增长和气候变化导致的粮食短缺预计在不久的将来会成为一个迫切需要解决的问题。传统育种技术,特别是杂交育种和诱变育种,在获得具有所需性状的种子和幼苗方面效率低下且耗时。因此,迫切需要高效植物育种的新方法。基因组编辑育种受到了广泛关注,因为与传统方法相比,它可以有效地修饰目标基因以获得所需性状。在已开发用于基因组编辑的可编程序列特异性核酸酶中,CRISPR-Cas12a和CRISPR-MAD7核酸酶在谷物、蔬菜和水果的基因组编辑应用中越来越广泛地被采用。此外,MAD7的改进变体ST8已被开发出来以提高基因组编辑效率,并具有应用于作物育种的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01a3/11375424/c759ec3b4dc2/74_022-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01a3/11375424/c08b58cc8b2a/74_022-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01a3/11375424/e419036713e5/74_022-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01a3/11375424/c759ec3b4dc2/74_022-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01a3/11375424/c08b58cc8b2a/74_022-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01a3/11375424/e419036713e5/74_022-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/01a3/11375424/c759ec3b4dc2/74_022-g003.jpg

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CRISPR/Cas9 gene editing technology: a precise and efficient tool for crop quality improvement.CRISPR/Cas9 基因编辑技术:一种用于改善作物品质的精确高效工具。
Planta. 2023 Jul 3;258(2):36. doi: 10.1007/s00425-023-04187-z.
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Boosting genome editing efficiency in human cells and plants with novel LbCas12a variants.利用新型 LbCas12a 变体提高人类细胞和植物中的基因组编辑效率。
Genome Biol. 2023 Apr 30;24(1):102. doi: 10.1186/s13059-023-02929-6.
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Front Plant Sci. 2023 Mar 13;14:1133036. doi: 10.3389/fpls.2023.1133036. eCollection 2023.
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A MAD7-based genome editing system for Escherichia coli.基于 MAD7 的大肠杆菌基因组编辑系统。
Microb Biotechnol. 2023 May;16(5):1000-1010. doi: 10.1111/1751-7915.14234. Epub 2023 Mar 16.
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