Evidence map›Paper›PMID 38315256›Full record

ArticleMolecular genetics and genomics : MGG2024

CRISPR/Cas9-mediated efficient white genome editing in the black soldier fly Hermetia illucens.

Zhuoxiao Sui, Qi Wu, Jin Geng, Jinhua Xiao, Dawei Huang

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Article in Molecular genetics and genomics : MGG, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Zhuoxiao SuiCollege of Life Sciences, Nankai University, Tianjin, 300071, China.
Qi WuCollege of Life Sciences, Nankai University, Tianjin, 300071, China.
Jin GengCollege of Life Sciences, Nankai University, Tianjin, 300071, China.
Jinhua XiaoCollege of Life Sciences, Nankai University, Tianjin, 300071, China. xiaojh@nankai.edu.cn.ORCID http://orcid.org/0000-0001-6105-8976
Dawei HuangCollege of Life Sciences, Nankai University, Tianjin, 300071, China. huangdw@nankai.edu.cn.

Funding

National Natural Science Foundation of China 31830084National Natural Science Foundation of China 31970440
6 · The paper itself

Abstract

The CRISPR/Cas9 system is the most straightforward genome-editing technology to date, enabling genetic engineering in many insects, including the black soldier fly, Hermetia illucens. The white gene plays a significant role in the multifarious life activities of insects, especially the pigmentation of the eyes. In this study, the white gene of H. illucens (Hiwhite) was cloned, identified, and bioinformatically analysed for the first time. Using quantitative real-time polymerase chain reaction (qPCR), we found that the white gene was expressed in the whole body of the adult flies, particularly in Malpighian tubules and compound eyes. Furthermore, we utilised CRISPR/Cas9-mediated genome-editing technology to successfully generate heritable Hiwhite mutants using two single guide RNAs. During Hiwhite genome editing, we determined the timing, method, and needle-pulling parameters for embryo microinjection by observing early embryonic developmental features. We used the CasOT program to obtain highly specific guide RNAs (gRNAs) at the genome-wide level. According to the phenotypes of Hiwhite knockout strains, the pigmentation of larval stemmata, imaginal compound eyes, and ocelli differed from those of the wild type. These phenotypes were similar to those observed in other insects harbouring white gene mutations. In conclusion, our results described a detailed white genome editing process in black soldier flies, which lays a solid foundation for intensive research on the pigmentation pathway of the eyes and provides a methodological basis for further genome engineering applications in black soldier flies.

Indexed as

DipteraGene EditingAnimalsCRISPR-Cas SystemsMutationRNA, Guide, CRISPR-Cas SystemsRNA, Guide, CRISPR-Cas SystemsCas9CRISPREmbryo microinjectionHermetia illucensSpecific single guide RNAWhite

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.