2024
DOI: 10.1002/ps.7992
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Identification and RNAi‐based function analysis of trehalase family genes in Frankliniella occidentalis (Pergande)

Xiaobin Zheng,
Jiangjiang Yuan,
Kanghua Qian
et al.

Abstract: BACKGROUNDInsects utilize trehalases (TREs) to regulate energy metabolism and chitin biosynthesis, which are essential for their growth, development, and reproduction. TREs can therefore be used as potential targets for future insecticide development. However, the roles of TREs in Frankliniella occidentalis (Pergande), a serious widespread agricultural pest, remain unclear.RESULTSThree TRE genes were identified in F. occidentalis and cloned, and their functions were then investigated via feeding RNA interferen… Show more

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Cited by 5 publications
(2 citation statements)
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“…The three new compounds-6d, 6e, and 6f-inhibited the trehalase activity in S. frugiperda larvae and downregulated the expression of both TRE1 and TRE2, consequently restricting the energy availability in the insects. Silencing the trehalase gene of Frankliniella occidentalis also led to significantly downregulated levels of enzymes associated with the energy metabolism pathway [44].…”
Section: Discussionmentioning
confidence: 99%
“…The three new compounds-6d, 6e, and 6f-inhibited the trehalase activity in S. frugiperda larvae and downregulated the expression of both TRE1 and TRE2, consequently restricting the energy availability in the insects. Silencing the trehalase gene of Frankliniella occidentalis also led to significantly downregulated levels of enzymes associated with the energy metabolism pathway [44].…”
Section: Discussionmentioning
confidence: 99%
“…The dsRNA primers (Table S1) targeting specific FoRab genes and the control gene (EGFP) were designed to minimize potential off-target effects using the Snapdragon tool (https://www.flyrnai.org/cgi-bin/RNAi_find_ primers.pl). RNAi experiments were performed according to protocols established in our laboratory, 52 and all dsRNAs were synthesized using the T7 Ribomax Express RNAi reagent (Promega, Madison). Approximately 400 first-instar nymphs were fed a 0.2 mL solution containing 0.5 μg/μL target gene dsRNA in a 10% sucrose solution for 24 h in a designated feeding chamber.…”
Section: ■ Materials and Methodsmentioning
confidence: 99%