Cloning and functional analysis of the chitin synthase in Frankliniella occidentalis
Author of the article:TANG Ying-Xi** ZHENG Xiao-Bin CAO Hong-Yi YUAN Jiang-Jiang CHEN Si-Rui WANG Jing WU Yu-Lei Z
Author's Workplace:State Key Laboratory of Vegetable Biobreeding, Institute of Vegetables and Flowers, Chinese Academy of Agricultural Sciences, Beijing 100081, China
Key Words:Frankliniella occidentalis; chitin synthetase; growth and development; RNAi
Abstract:
[Aim] To investigate the impact of chitin synthase
(CHS) on the growth and
development of Frankliniella occidentalis,
aiming to identify a potential target for controlling F. occidentalis. [Methods]
The CHS gene of F.
occidentalis was cloned and named Fochs,
and its function was investigated using RNA interference (RNAi) technology. [Results] The full-length open reading frame of the Fochs gene was 4 656 bp, encoding 1 551
amino acids, and the predicted molecular weight was 176.02 kD. The conserved
domain was Glyco-tranf-GTA-type superfamily. The phylogenetic tree indicated
that the Fochs had the closest
genetic relationship with the CHS of Thrips palmi. RT-qPCR results
demonstrated that the Fochs gene was
expressed at all stages of the growth and development of F. occidentalis, with the highest expression in the 2nd instar
nymphs, followed by the pro-pupae. After silencing Fochs for 120 h, the mortality rates of the 2nd instar nymphs and
pro-pupae was significantly increased (P < 0.01), while the pupation rate and eclosion
rate was significantly decreased (P <
0.01). Both nymphs and pupae exhibited morphological changes such
as wrinkled cuticle, reduced body size, and deformity, with almost no effect on
newly eclosed adults. [Conclusion]
The chitin synthase gene plays a significant role in the growth and
development of F. occidentalis, making it a potential target for
precise and environmentally friendly control through RNAi-mediated approaches.