4.6 Article

The Roles of E93 and Kr-h1 in Metamorphosis of Nilaparvata lugens

期刊

FRONTIERS IN PHYSIOLOGY
卷 9, 期 -, 页码 -

出版社

FRONTIERS MEDIA SA
DOI: 10.3389/fphys.2018.01677

关键词

E93; Kr-h1; Nilaparvata lugens; metamorphosis; RNAi

资金

  1. National Natural Science Foundation of China [31501637]
  2. Rice Pest Management Research Group of the Agricultural Science and Technology Innovation Program of Chinese Academy of Agricultural Sciences
  3. China National Rice Industrial Technology System [CARS-01-35]
  4. National Key Research and Development Program of China
  5. National Key R&D Program of China [2016YFD0200801]
  6. Fundamental Research Funds of the Central Public Welfare Research Institute [2017RG005]

向作者/读者索取更多资源

Metamorphosis is a crucial process in insect development. Ecdysone-induced protein 93 (E93) is a determinant that promotes adult metamorphosis in both hemimetabolous and holometabolous insects. Kruppel-homolog 1 (Kr-h1), an early juvenile hormone (JH)-inducible gene, participates in JH signaling pathway controlling insect metamorphosis. In the current study, an E93 cDNA (NlE93) and two Kr-h1 cDNA variants (NlKr-h1-a and NlKr-h1-b) were cloned from Nilaparvata lugens (Stal), one of the most destructive hemimetabolous insect pests on rice. Multiple sequence alignment showed that both NlE93 and NlKr-h1 share high identity with their orthologs from other insects. The expression patterns revealed that decreasing NlKr-h1 mRNA levels were correlated with increasing NlE93 mRNA levels and vice versa. Moreover, RNA interference (RNAi) assays showed that the knockdown of one of the two genes resulted in significantly upregulated expression of the other. Correspondingly, phenotypical observation of the RNAi insects revealed that depletion of NlE93 prevented nymph-adult transition (causing a supernumerary nymphal instar), while depletion of NlKr-h1 triggered precocious formation of incomplete adult features. The results suggest that Nlkr-h1 and NlE93 are mutual repressors, fitting into the MEKRE93 pathway. The balance between these two genes plays a critical role in the metamorphosis of N. lugens determining the proper timing for activating metamorphosis during the nymphal stage.

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