The insect brain regulates the activity of the prothoracic glands to secrete ecdysteroids, which affect growth, molting, and metamorphosis. Here we report the identification of a novel prothoracicostatic factor and its receptor in the silkworm Bombyx mori. The prothoracicostatic factor purified from pupal brains of B. mori is a decapeptide with the conserved structure of an insect myosuppressin and thus named Bommo-myosuppressin. Bommo-myosuppressin dose dependently suppressed the cAMP level and inhibited ecdysteroidogenesis in the larval prothoracic glands at much lower concentrations than the prothoracicostatic peptide, the other prothoracicostatic factor reported previously. In vitro analyses using a prothoracic gland incubation method revealed that Bommo-myosuppressin and prothoracicostatic peptide regulate the prothoracic gland activity via different receptors. In situ hybridization and immunohistochemistry revealed the existence of Bommo-myosuppressin in the brain neurosecretory cells projecting to neurohemal organs in which it is stored. We also identified and functionally characterized a specific receptor for Bommo-myosuppressin and showed its high expression in the prothoracic glands. All these results suggest that Bommo-myosuppressin functions as a prothoracicostatic hormone and plays an important role in controlling insect development.
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http://dx.doi.org/10.1074/jbc.M500308200 | DOI Listing |
Front Physiol
December 2024
School of Agriculture and Biotechnology, Shenzhen Campus of Sun Yat-sen University, Shenzhen, China.
Introduction: The juvenile hormone (JH) and 20-hydroxyecdysone (20E) are the central regulating hormones of insect development. The timing of their secretion usually leads to developmental transitions.
Methods: The developmental transitions were evaluated via the starvation treatment and the expressions of two key metamorphosis inducing factor in .
Background: Parasitic wasps manipulate host development for successful parasitization. When the host Ostrinia furnacalis is parasitized by the parasitoid Macrocentrus cingulum, its larvae fail to pupate and are consumed as nutrition by the wasp larvae. However, the mechanism by which M.
View Article and Find Full Text PDFInsect Biochem Mol Biol
December 2024
Guangdong Provincial Key Laboratory of Insect Developmental Biology and Applied Technology, Guangzhou Key Laboratory of Insect Development Regulation and Application Research, Institute of Insect Science and Technology, School of Life Sciences, South China Normal University, Guangzhou, 510000, China; Guangmeiyuan R&D Center, Guangdong Provincial Key Laboratory of Insect Developmental Biology and Applied Technology, South China Normal University, Meizhou, 514000, China. Electronic address:
The evolution of insect metamorphosis has profoundly influenced their successful adaptation and diversification. Two key physiological processes during insect metamorphosis are notable: wing maturation and prothoracic gland (PG) histolysis. The ecdysone-induced protein 93 (E93) is a transcription factor indispensable for metamorphosis.
View Article and Find Full Text PDFbioRxiv
October 2024
Department of Genetics, Cell Biology and Development, University of Minnesota, Minneapolis, MN 55455.
Toys are us (Trus) is the ortholog of mammalian Programmed Cell Death 2-Like (PDCD2L), a protein that has been implicated in ribosome biogenesis, cell cycle regulation, and oncogenesis. In this study, we examined the function of Trus during development. CRISPR/Cas9 generated null mutations in lead to partial embryonic lethality, significant larval developmental delay, and complete pre-pupal lethality.
View Article and Find Full Text PDFPestic Biochem Physiol
November 2024
College of Agriculture, Guangxi University, Nanning, Guangxi 530004, PR China; Guangxi Key Laboratory of Agro-Environment and Agric-Products Safety, National Demonstration Center for Experimental Plant Science Education, College of Agriculture, Guangxi University, Nanning, Guangxi 530004, PR China. Electronic address:
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