SeBLOS2 knockout via CRISPR/Cas9 leads to the loss of larval integument coloration in Spodoptera exigua (Lepidoptera: Noctuidae).
Jing ZhaoYiping JiangAry HoffmannYongan TanLiubin XiaoPublished in: Archives of insect biochemistry and physiology (2023)
CRISPR/Cas9 technology is a precise and powerful tool for functionally exploring insect genes. The present study tested CRISPR/Cas9 as a way of undertaking effective gene mutagenesis in an important agricultural pest, the beet armyworm Spodoptera exigua. Based on a S. exigua transcriptome database, the entire complementary DNA sequence of SeBLOS2 encoding 140 amino acid residues was cloned. The gene was highly expressed in late larval stages (L3-L5). Using the CRISPR/Cas9 method, SeBLOS2 was knocked out by altering two sites in the coding region. This resulted in 70%-74% of the G0 generation (L4-L5) larvae displaying mosaic translucent integument. Four different mutations occurred at SeBLOS2-specific target sites, as demonstrated by further polymerase chain reaction-based genotypic analysis. Homozygote mutant L3 larvae were obtained in the G1 generation, with complete loss of white stripes and spots on their larval integument. These results demonstrate a crucial role of SeBLOS2 in integument pigmentation and suggest that the gene can act as a suitable nonlethal marker for functional research on genes in S. exigua and other Lepidopteran pests.
Keyphrases
- crispr cas
- genome editing
- genome wide
- aedes aegypti
- genome wide identification
- drosophila melanogaster
- copy number
- amino acid
- dna methylation
- zika virus
- genome wide analysis
- gene expression
- transcription factor
- risk assessment
- heavy metals
- single cell
- emergency department
- bioinformatics analysis
- cell free
- circulating tumor
- rna seq
- data analysis
- circulating tumor cells