生物
基因敲除
血淋巴
RNA干扰
寄主(生物学)
蛹
基因沉默
非翻译区
抄写(语言学)
寄生
转录因子
RNA沉默
细胞生物学
下调和上调
三素数非翻译区
小发夹RNA
信使核糖核酸
遗传学
RNA结合蛋白
小干扰RNA
核糖核酸
分子生物学
模式生物
免疫
生殖器鳞翅目
作者
Yurong Zhang,Yan Du,Yipei Dong,Qian Wang,Yuanshi Cai,Jian Hu
标识
DOI:10.1111/1744-7917.70209
摘要
Abstract Parasitic wasps have evolved intricate strategies to manipulate host development for the benefit of their offspring. In the lepidopteran host Ostrinia furnacalis , parasitism by Macrocentrus cingulum leads to pupation failure; however, the molecular mechanisms remain unclear. Here, we demonstrate that miR‐281a‐5p, upregulated in the hemolymph of parasitized host larvae, inhibits pupation by directly targeting ecdysone‐induced protein 93F ( OfE93 ), a crucial transcription factor involved in metamorphosis. A dual‐luciferase assay confirmed that miR‐281a‐5p binds to the 3′ untranslated region of OfE93 . Moreover, injection of agomiR‐281a‐5p significantly reduced both transcript and protein levels of OfE93 in O. furnacalis larvae. RNA interference‐mediated knockdown of OfE93 partially replicated the effects of parasitism, causing pupation arrest in approximately 20% of O. furnacalis larvae. These findings reveal a microRNA‐based mechanism by which M. cingulum disrupts the host's endocrine‐driven metamorphosis, providing new insights into the molecular interactions between parasitoids and their hosts.
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