转录组
马尔皮基亚小管系统
生物
异型生物质的
基因
基因敲除
基因表达
中肠
转基因
遗传学
实时聚合酶链反应
基因表达谱
基因组
细胞生物学
计算生物学
代谢途径
鉴定(生物学)
RNA干扰
芳香烃受体
RNA序列
戒毒(替代医学)
基因表达调控
代谢组学
聚合酶链反应
核糖核酸
功能基因组学
毒理基因组学
候选基因
超家族
模式生物
作者
Long Jin,Cheng-Cheng Fan,Pengjun Xun,Zhixin Zhang,Haoran Kong,Haizheng Zhao,Yiou Pan,Qing-Li Shang
标识
DOI:10.1021/acs.jafc.5c12376
摘要
As a global pest, Spodoptera litura causes significant economic losses annually, making it imperative to investigate its metabolic detoxification mechanisms. The solute carrier (SLC) gene constitutes a superfamily of genes that can directly or indirectly influence the metabolic detoxification functions of insects. In this study, 108 SLC genes were identified via the S. litura genome database (ASM270686v3), and their expression patterns were analyzed through transcriptome analysis. Three candidate SLC genes with inducible expression characteristics in different tissues, namely, SLC22A5, SLC52A3, and SLC12A4, were selected for further experimental studies. The quantitative real-time polymerase chain reaction results indicated that following exposure to xenobiotics, SLC52A3 was expressed in both the midgut and Malpighian tubules, SLC22A5 expression was induced in the Malpighian tubules, and SLC12A4 was expressed in the midgut. Overexpression of SLC22A5, SLC52A3, and SLC12A4 in transgenic Drosophila conferred tolerance to xenobiotics. Furthermore, following the knockdown of SLC52A3 via RNA interference, the tolerance of S. litura to both cyantraniliprole and chlorantraniliprole significantly decreased. These results suggest that SLC genes may play roles in driving the development of xenobiotic tolerance in S. litura.
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