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1.
Insect Mol Biol ; 31(5): 543-550, 2022 10.
Article in English | MEDLINE | ID: mdl-35429082

ABSTRACT

CRISPR/Cas9 genome editing has now expanded to many insect species, including Tribolium castaneum. However, compared to Drosophila melanogaster, the CRISPR toolkit of T. castaneum is limited. A particularly apparent gap is the lack of Cas9 transgenic animals, which generally offer higher editing efficiency. We address this by creating and testing transgenic beetles expressing Cas9. We generated two different constructs bearing basal heat shock promoter-driven Cas9, two distinct 3' UTRs, and one containing Cas9 fused to EGFP by a T2A peptide. Analyses of Cas9 activity in each transgenic line demonstrated that both designs are capable of inducing CRISPR- mediated changes in the genome in the absence of heat induction. Overall, these resources enhance the accessibility of CRISPR/Cas9 genome editing for the Tribolium research community and provide a benchmark against which to compare future transgenic Cas9 lines.


Subject(s)
Tribolium , Animals , Animals, Genetically Modified , CRISPR-Cas Systems , Drosophila melanogaster/genetics , Gene Editing , Tribolium/genetics
2.
PLoS One ; 13(4): e0195977, 2018.
Article in English | MEDLINE | ID: mdl-29649291

ABSTRACT

The red flour beetle, Tribolium castaneum, is an important model insect and agricultural pest. However, many standard genetic tools are lacking or underdeveloped in this system. Here, we present a set of new reagents to augment existing Tribolium genetic tools. We demonstrate a new GAL4 driver line that employs the promoter of a ribosomal protein gene to drive expression of a UAS responder in the fat body. We also present a novel dual fluorescent reporter that labels cell membranes and nuclei with different fluorophores for the analysis of cellular morphology. This approach also demonstrates the functionality of the viral T2A peptide for bicistronic gene expression in Tribolium. To facilitate classical genetic analysis, we created lines with visible genetic markers by CRISPR-mediated disruption of the yellow and ebony body color loci with a cassette carrying an attP site, enabling future φC31-mediated integration. Together, the reagents presented here will facilitate more robust genetic analysis in Tribolium and serve as a blueprint for the further development of this powerful model's genetic toolkit.


Subject(s)
Genetic Techniques , Tribolium/genetics , Animals , CRISPR-Cas Systems , Gene Expression , Gene Order , Gene Targeting , Genes, Reporter , Genetic Vectors/genetics , Phenotype , Promoter Regions, Genetic , Transgenes
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