Detoxification gene families at the genome-wide level of Rhus gall aphid Schlechtendalia chinensis
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Abstract
The Rhus gall aphid Schlechtendalia chinensis uses the species Rhus chinensis as its primary host plant, on which galls are produced. The galls have medicinal properties and can be used in various situations due to their high tannin content. Detoxification enzymes play significant roles in the insect lifecycle. In this study, we focused on five detoxification gene families, i.e., glutathione-Stransferase (GST), ABC transporter (ABC), Carboxylesterase (CCE), cyto-chrome P450 (CYP), and UDP-glycosyltransferase (UDP), and manually annotated 144 detoxification genes of S. chinensis using genome-wide techniques. The detoxification genes appeared mostly on chromosome 1, where a total of two pair genes were identified to show tandem duplications. There were 38 gene pairs between genomes of S. chinensis and Acyrthosiphon pisum in the detoxification gene families by collinear comparison. Ka/Ks ratios showed that detoxification genes of S. chinensis were mainly affected by purification selection during evolution. The gene expression numbers of P450s and ABCs by transcriptome sequencing data were greater, while gene expression of CCEs was the highest, suggesting they might be important in the detoxification process. Our study has firstly identified the genes of the different detoxification gene families in the S. chinensis genome, and then analyzed their general features and expression, demonstrating the importance of the detoxification genes in the aphid and providing new information for further research.Citation
He H, Crabbe MJC, Ren Z (2022) 'Detoxification gene families at the genome-wide level of Rhus gall aphid Schlechtendalia chinensis', Genes, 13 (9) 1627Publisher
MDPIJournal
GenesPubMed ID
36140795PubMed Central ID
PMC9498883Additional Links
https://www.mdpi.com/2073-4425/13/9/1627https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9498883/
Type
ArticleLanguage
enISSN
2073-4425EISSN
2073-4425Sponsors
This study was partially supported by The National Natural Science Foundation of China (31870366), Shanxi International Science and Technology Cooperation Project (201803D421051), Research Project Supported by Shanxi Scholarship Council of China (2020-018), the National High Technology Research and Development “863” Program (2014AA021802).ae974a485f413a2113503eed53cd6c53
10.3390/genes13091627
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