Hiura Takeshi, Yoshida Hibiki, Miyata Umi, Asami Tadao, Suzuki Yoshihito
United Graduate School of Agricultural Science, Tokyo University of Agriculture and Technology, 3-5-8 Saiwai-cho, Fuchu-shi, Tokyo 183-0054, Japan.
Department of Food and Life Sciences, College of Agriculture, Ibaraki University, 3-21-1 Chuo, Ami-machi, Inashiki-gun, Ibaraki 300-0393, Japan.
Insects. 2023 Jul 2;14(7):598. doi: 10.3390/insects14070598.
Gall-inducing insects often contain high concentrations of phytohormones, such as auxin and cytokinin, which are suggested to be involved in gall induction, but no conclusive evidence has yet been obtained. There are two possible approaches to investigating the importance of phytohormones in gall induction: demonstrating either that high phytohormone productivity can induce gall-inducing ability in non-gall-inducing insects or that the gall-inducing ability is inhibited when phytohormone productivity in galling insects is suppressed. In this study, we show that the overexpression of , which encodes an aromatic aldehyde synthase (AAS) responsible for the rate-limiting step in indoleacetic acid (IAA) biosynthesis in a galling sawfly ( sp.) that contains high levels of endogenous IAA, conferred high IAA productivity on , as the model system. This result strongly suggests that PonAAS2 can also confer high IAA productivity on low-IAA-producing insects. We also successfully identified an inhibitor of PonAAS2 in a chemical library. This highly selective inhibitor showed stronger inhibitory activity against AAS than against aromatic amino acid decarboxylase, which belongs to the same superfamily as AAS. We also confirm that this inhibitor clearly inhibited IAA productivity in the high-IAA-producing engineered here.
致瘿昆虫通常含有高浓度的植物激素,如生长素和细胞分裂素,这些激素被认为与瘿瘤诱导有关,但尚未获得确凿证据。研究植物激素在瘿瘤诱导中重要性有两种可能的方法:一是证明高植物激素产生能力能诱导非致瘿昆虫产生致瘿能力,二是证明当致瘿昆虫的植物激素产生能力受到抑制时,其致瘿能力也会受到抑制。在本研究中,我们以一种含有高水平内源性吲哚乙酸(IAA)的致瘿叶蜂( 种)为模型系统,表明编码负责吲哚乙酸(IAA)生物合成限速步骤的芳香醛合酶(AAS)的 的过表达赋予了 高IAA产生能力。这一结果强烈表明,PonAAS2也能赋予低IAA产生昆虫高IAA产生能力。我们还在一个化学文库中成功鉴定出了PonAAS2的一种抑制剂。这种高度选择性的抑制剂对AAS的抑制活性比对与AAS属于同一超家族的芳香氨基酸脱羧酶更强。我们还证实,这种抑制剂在此处构建的高IAA产生的 中明显抑制了IAA产生能力。