Enhancements of the CRISPR-Cas System in the Silkworm <i>Bombyx mori</i>

The silkworm (<i>Bombyx mori</i>) 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.

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Publication Details

Journal
The CRISPR Journal
Published
2025-03-28
DOI
https://doi.org/10.1089/crispr.2024.0089
Citations
4
Primary Topic
CRISPR and Genetic Engineering
Type
article
Field-Weighted Citation Impact
3.22
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article

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

Yoko Takasu, Takuya Tsubota, Naoyuki Yonemura, Hideki Sezutsu
4 citations
The CRISPR Journal
CRISPR and Genetic Engineering
3.22
article

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

Yoko Takasu, Takuya Tsubota, Naoyuki Yonemura, Hideki Sezutsu
article en
4 citations

Abstract

The silkworm (<i>Bombyx mori</i>) 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.

The CRISPR JournalVol. 8(2)
National Agriculture and Food Research Organization (JP), Institute of Agrobiological Sciences (JP)
Zero hunger
Openalex Percentile: Top 9%
CRISPR and Genetic Engineering
3.22
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