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Kr-h1, a Cornerstone Gene in Insect Life History

Journal

FRONTIERS IN PHYSIOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fphys.2022.905441

Keywords

Kr-h1; metamorphosis; reproduction; juvenile hormone; ecdysone; behavioral plastisity; neuronal morphogenesis; embryogenesis

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Funding

  1. National Natural Science Foundation of China [31970465]
  2. University Nursing Program for Young Scholars with Creative Talents in Heilongjiang Province [UNPYSCT-2018080]
  3. Scientific Research Foundation for Postdoctors in Heilongjiang Province of China [LBH-Q19165]

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The insect life cycle is regulated by hormones and their downstream effectors. Kruppel homolog1 (Kr-h1) is an important effector that mediates the actions of juvenile hormone (JH) and 20-hydroxyecdysone (20E) in insects. The expression of Kr-h1 fluctuates during insect development and is closely linked to its function in different stages of the insect's life, including antimetamorphic effects, promotion of ovarian development and vitellogenesis, regulation of behavioral plasticity and caste identity, neuronal morphogenesis, maturation of sexual behavior, embryogenesis, and metabolic homeostasis.
Insect life cycle is coordinated by hormones and their downstream effectors. Kruppel homolog1 (Kr-h1) is one of the crucial effectors which mediates the actions of the two critical hormones of insects, the juvenile hormone (JH) and 20-hydroxyecdysone (20E). It is a transcription factor with a DNA-binding motif of eight C2H2 zinc fingers which is found to be conserved among insect orders. The expression of Kr-h1 is fluctuant during insect development with high abundance in juvenile instars and lower levels in the final instar and pupal stage, and reappearance in adults, which is governed by the coordination of JH, 20E, and miRNAs. The dynamic expression pattern of Kr-h1 is closely linked to its function in the entire life of insects. Over the past several years, accumulating studies have advanced our understanding of the role of Kr-h1 during insect development. It acts as a universal antimetamorphic factor in both hemimetabolous and holometabolous species by directly inhibiting the transcription of 20E signaling genes Broad-Complex (Br-C) and Ecdysone induced protein 93F (E93), and steroidogenic enzyme genes involved in ecdysone biosynthesis. Meanwhile, it promotes vitellogenesis and ovarian development in the majority of studied insects. In addition, Kr-h1 regulates insect behavioral plasticity and caste identity, neuronal morphogenesis, maturation of sexual behavior, as well as embryogenesis and metabolic homeostasis. Hence, Kr-h1 acts as a cornerstone regulator in insect life.

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