昆虫学报 ›› 2024, Vol. 67 ›› Issue (4): 589-594.doi: 10.16380/j.kcxb.2024.04.015

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褐飞虱翅型分化调控机制的研究进展

陈孙杰, 徐海君*   

  1. (浙江大学昆虫科学研究所, 水稻生物育种国家重点实验室, 杭州 310058)
  • 出版日期:2024-04-20 发布日期:2024-05-24

Research progresses of the regulatory mechanisms of wing polyphenism in the brown planthopper, Nilaparvata lugens (Hemiptera: Delphacidae)

CHEN Sun-Jie, XU Hai-Jun*   

  1.  (State Key Laboratory of Rice Biology and Breeding, Institute of Insect Sciences, Zhejiang University, Hangzhou 310058, China)
  • Online:2024-04-20 Published:2024-05-24

摘要:  昆虫翅多型作为生物可塑性发育的典型代表,是昆虫对复杂多变环境适应进化的结果。褐飞虱Nilaparvata lugens是一种典型的翅多型昆虫,若虫可发育成短翅型或长翅型成虫,后者的远距离迁飞特性造成褐飞虱在亚洲稻区大面积为害。20世纪60年代以来,前人针对褐飞虱翅多型的发生机理进行了大量研究,发现种群密度、寄主植物质量、温度和光周期等诸多环境因子以及保幼激素均能够影响翅型比例。近20年来,得益于基因组学、 RNAi和基因编辑等生物技术的发展,褐飞虱翅型分化的分子机制研究取得了突破性进展,发现了褐飞虱翅型分化的开关基因FoxO,沉默或敲除FoxO会导致飞虱发育为长翅型;而胰岛素信号通路能够磷酸化FoxO抑制其进入细胞核,从而参与翅型分化调控;锌指转录因子Zfh1能够以启动子结合的方式调节FoxO的转录,与胰岛素信号通路平行调控翅型分化;另一个锌指转录因子Rotund能够与FoxO互作共同调控褐飞虱翅多型。此外,性别决定基因Transformer-2和c-Jun氨基末端激酶通路等也能够影响翅型分化,表明褐飞虱的翅型分化存在多样化的分子调控机制。鉴于半翅目不同亚目间的翅多型机制均有所不同,对褐飞虱翅型分化机制的解析远不足以阐明半翅目乃至整个昆虫纲的翅多型机制,但其研究成果能够引领未来对昆虫翅多型机制的探索研究,并加深人们对昆虫翅及组织可塑性发育与进化的理解。

关键词: 褐飞虱, 半翅目, 翅多型, 表型可塑性, 保幼激素, 转录因子

Abstract: Insect wing polyphenism, as a typical example of the developmental plasticity of organisms, is the result of evolutionary adaptation to complex and variable environments. The brown planthopper (BPH), Nilaparvata lugens, is a representative model of insect wing polyphenism, and its nymphs have the option of developing into shortwinged or longwinged adults. The ability of developing into longwinged morphs enables BPHs to migrate over long distances, causing an infestation over a wide geographic rice planting area in Asia. Since the 1960s, there has been extensive research into the mechanisms behind wing polyphenism in BPHs, revealing that numerous environmental factors such as population density, host plant quality, temperature and photoperiod, and juvenile hormone can all influence the proportion of wing morphs. In the past 20 years, facilitated by the rapid development of biotechnologies in genomics, RNAi and gene editing, a breakthrough finding has been achieved in wing polyphenism of BPHs. FoxO has been identified as a switch gene for wing polyphenism in BPHs, where silencing or knocking out FoxO leads to the development of long-winged adults. Meanwhile, the insulin signaling pathway can inhibit FoxO from entering the nucleus by phosphorylating it, thus participating in wing polyphenism regulation. The zinc finger transcription factor Zfh1 can regulate the transcription of FoxO through promoter binding, paralleling the insulin signaling pathway in controlling wing polyphenism. Another zinc finger transcription factor, Rotund, can interact with FoxO to co-regulate wing polyphenism of BPHs. Additionally, the sex determination gene Transformer-2 and the c-Jun N-terminal kinase pathway can also influence wing polyphenism, indicating the presence of diverse molecular regulatory mechanisms for wing polyphenism in BPHs. Given the differences in the mechanisms of wing polyphenism among different suborders of Hemiptera, the elucidation of mechanisms in BPHs is far from fully explaining the mechanisms of wing polymorphism in Hemiptera or even the entire class of insects. However, these findings position themselves at the edge of wing polyphenism in insects and deepen our understanding of developmental plasticity and evolution of insect wings as well as other tissues.

Key words: Nilaparvata lugens, Hemiptera, wing polyphenism, phenotypic plasticity, juvenile hormones, transcription factor