Udandarao Naga Jyothi, Yamashita Yuki, Ushima Ryo, Tsuchida Tsutomu, Bessho-Uehara Kanako
Graduate School of Life Sciences Tohoku University Sendai Miyagi Japan.
Graduate School of Science and Engineering for Education University of Toyama Toyama Toyama Japan.
Plant Direct. 2025 Aug 20;9(8):e70099. doi: 10.1002/pld3.70099. eCollection 2025 Aug.
Gall-inducing insects manipulate host plant development, redirecting cellular fate and physiological processes to form novel structures. This phenomenon is even more intriguing when the host itself is a holoparasitic plant with minimal photosynthetic capacity. In the stem of , the weevil forms galls that unexpectedly activate photosynthesis, in contrast to the typical suppression of photosynthetic activity observed in leaf-derived galls. This reversal of the usual source-to-sink transition highlights a unique form of insect-induced organogenesis. To elucidate the underlying mechanisms, we performed transcriptomic, histological, and physiological analyses of these galls. RNA-seq across four developmental stages identified differentially expressed genes and associated gene ontology terms. Consistent with histological observations, genes related to cell division and the cell cycle were upregulated in early stage but decreased as the gall matured. Similar to leaf-derived galls, we found high expression of and meristem-related homeobox genes in early gall development, suggesting that induction of cell division is involved in various gall types. Interestingly, the expression of genes related to floral organ development increased through gall development. However, their expression patterns showed a marked temporal shift: Floral organ identity genes were highly expressed at the initial gall stage, whereas floral transition genes were activated later. This suggests that the weevil triggers ectopic activation of the flowering pathway in non-floral tissues, potentially redirecting the typical flowering cascade to drive gall formation. Consistent with previous findings, photosynthesis-related genes were highly expressed in later stage of galls, despite the host being a holoparasitic plant. Shading experiments confirmed that photosynthesis is crucial for both gall and the weevil growth. This study highlights how gall-inducers can co-opt host resources and genetic pathways, offering new insights into the complexity of plant-insect interactions.
致瘿昆虫操控宿主植物的发育,改变细胞命运和生理过程以形成新的结构。当宿主本身是光合能力极低的全寄生植物时,这种现象就更具吸引力了。在 的茎中,象鼻虫形成的瘿意外地激活了光合作用,这与在叶瘿中观察到的典型光合活性抑制形成对比。这种通常的源 - 库转换的逆转突出了一种独特的昆虫诱导器官发生形式。为了阐明潜在机制,我们对这些瘿进行了转录组学、组织学和生理学分析。对四个发育阶段进行的RNA测序确定了差异表达基因及相关的基因本体术语。与组织学观察结果一致,与细胞分裂和细胞周期相关的基因在早期上调,但随着瘿的成熟而减少。与叶瘿相似,我们发现在瘿发育早期 和分生组织相关的同源框基因高表达,表明细胞分裂的诱导参与了各种瘿类型。有趣的是,与花器官发育相关的基因在瘿发育过程中表达增加。然而,它们的表达模式显示出明显的时间变化:花器官特征基因在瘿形成初期高表达,而花转变基因在后期被激活。这表明象鼻虫在非花组织中触发了开花途径的异位激活,可能重定向典型的开花级联反应以驱动瘿的形成。与之前的研究结果一致,尽管宿主是全寄生植物,但与光合作用相关的基因在瘿的后期高表达。遮光实验证实光合作用对瘿和象鼻虫的生长都至关重要。这项研究突出了致瘿者如何利用宿主资源和遗传途径,为植物 - 昆虫相互作用的复杂性提供了新的见解。