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Expanding the plant genome editing toolbox with recently developed CRISPR–Cas systems
https://tokushima-u.repo.nii.ac.jp/records/2009987
https://tokushima-u.repo.nii.ac.jp/records/200998799d26412-8249-454b-bb0d-b48c77bb98a3
名前 / ファイル | ライセンス | アクション |
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Item type | 文献 / Documents(1) | |||||||||||
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公開日 | 2022-06-15 | |||||||||||
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アクセス権 | open access | |||||||||||
資源タイプ | ||||||||||||
資源タイプ識別子 | http://purl.org/coar/resource_type/c_6501 | |||||||||||
資源タイプ | journal article | |||||||||||
出版社版DOI | ||||||||||||
識別子タイプ | DOI | |||||||||||
関連識別子 | https://doi.org/10.1093/plphys/kiac027 | |||||||||||
言語 | ja | |||||||||||
関連名称 | 10.1093/plphys/kiac027 | |||||||||||
出版タイプ | ||||||||||||
出版タイプ | VoR | |||||||||||
出版タイプResource | http://purl.org/coar/version/c_970fb48d4fbd8a85 | |||||||||||
タイトル | ||||||||||||
タイトル | Expanding the plant genome editing toolbox with recently developed CRISPR–Cas systems | |||||||||||
言語 | en | |||||||||||
タイトル別表記 | ||||||||||||
その他のタイトル | Plant genome editing by CRISPR–Cas systems | |||||||||||
言語 | en | |||||||||||
著者 |
和田, 直樹
× 和田, 直樹× 刑部, 敬史
WEKO
664
× 刑部, 祐里子 |
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抄録 | ||||||||||||
内容記述タイプ | Abstract | |||||||||||
内容記述 | Since its first appearance, CRISPR–Cas9 has been developed extensively as a programmable genome-editing tool, opening a new era in plant genome engineering. However, CRISPR–Cas9 still has some drawbacks, such as limitations of the protospacer-adjacent motif (PAM) sequence, target specificity, and the large size of the cas9 gene. To combat invading bacterial phages and plasmid DNAs, bacteria and archaea have diverse and unexplored CRISPR–Cas systems, which have the potential to be developed as a useful genome editing tools. Recently, discovery and characterization of additional CRISPR–Cas systems have been reported. Among them, several CRISPR–Cas systems have been applied successfully to plant and human genome editing. For example, several groups have achieved genome editing using CRISPR–Cas type I-D and type I-E systems, which had never been applied for genome editing previously. In addition to higher specificity and recognition of different PAM sequences, recently developed CRISPR–Cas systems often provide unique characteristics that differ from well-known Cas proteins such as Cas9 and Cas12a. For example, type I CRISPR–Cas10 induces small indels and bi-directional long-range deletions ranging up to 7.2 kb in tomatoes (Solanum lycopersicum L.). Type IV CRISPR–Cas13 targets RNA, not double-strand DNA, enabling highly specific knockdown of target genes. In this article, we review the development of CRISPR–Cas systems, focusing especially on their application to plant genome engineering. Recent CRISPR–Cas tools are helping expand our plant genome engineering toolbox. | |||||||||||
言語 | en | |||||||||||
書誌情報 |
en : Plant Physiology 巻 188, 号 4, p. 1825-1837, 発行日 2022-01-31 |
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収録物識別子タイプ | ISSN | |||||||||||
収録物識別子 | 15322548 | |||||||||||
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収録物識別子タイプ | ISSN | |||||||||||
収録物識別子 | 00320889 | |||||||||||
出版者 | ||||||||||||
出版者 | Oxford University Press | |||||||||||
言語 | en | |||||||||||
出版者 | ||||||||||||
出版者 | American Society of Plant Biologists | |||||||||||
言語 | en | |||||||||||
権利情報 | ||||||||||||
言語 | en | |||||||||||
権利情報 | This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial reuse, please contact journals.permissions@oup.com | |||||||||||
EID | ||||||||||||
識別子 | 384428 | |||||||||||
識別子タイプ | URI | |||||||||||
言語 | ||||||||||||
言語 | eng |