Enhancements of the CRISPR-Cas System in the Silkworm Bombyx mori

被引:0
作者
Tsubota, Takuya [1 ]
Takasu, Yoko [2 ]
Yonemura, Naoyuki [1 ]
Sezutsu, Hideki [3 ]
机构
[1] Natl Agr & Food Res Org, Inst Agrobiol Sci, Silkworm Res Grp, Tsukuba, Ibaraki 3058634, Japan
[2] Natl Agr & Food Res Org, Inst Agrobiol Sci, Silk Mat Res Grp, Tsukuba, Japan
[3] Natl Agr & Food Res Org, Inst Agrobiol Sci, Div Silk Producing Insect Biotechnol, Tsukuba, Japan
来源
CRISPR JOURNAL | 2025年 / 8卷 / 02期
基金
日本科学技术振兴机构;
关键词
MESSENGER-RNA; GENOME; ZEBRAFISH;
D O I
10.1089/crispr.2024.0089
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The silkworm (Bombyx mori) is a lepidopteran model insect that has been utilized for basic research and industrial applications. In this species, transcription activator-like effector nucleases (TALENs) have been found to function efficiently, and we previously developed a TALEN-mediated genome editing system for knockout and knock-in experiments using plasmids and single-stranded oligodeoxynucleotides (ssODNs) as donors. By contrast, clustered regularly interspaced short palindromic repeats (CRISPR)-CRISPR-associated protein 9 (Cas9)-mediated genome editing, especially for gene integration, remains limited. In this study, we attempted to improve CRISPR-Cas systems to expand the utility of genome editing in the silkworm. Codon optimization of Cas9 improved genome editing efficiency, and single-guide RNA utilization also resulted in a higher genome editing efficiency than crRNA/tracrRNA when Cas9 messenger RNA (mRNA) was used. CRISPR-Cas12a-mediated genome editing and targeted sequence integration using ssODNs were both successfully performed. Overall, our study provides a robust technical platform that can facilitate basic and applied silkworm studies.
引用
收藏
页码:155 / 164
页数:10
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