Broad-Complex acts downstream of Met in juvenile hormone signaling to coordinate primitive holometabolan metamorphosis
Language English Country Great Britain, England Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
18171683
DOI
10.1242/dev.016097
PII: dev.016097
Knihovny.cz E-resources
- MeSH
- Metamorphosis, Biological * MeSH
- Models, Biological MeSH
- Coleoptera growth & development metabolism ultrastructure MeSH
- Insect Proteins chemistry genetics metabolism MeSH
- Juvenile Hormones metabolism MeSH
- Conserved Sequence MeSH
- Pupa ultrastructure MeSH
- Larva ultrastructure MeSH
- RNA, Messenger genetics metabolism MeSH
- Molecular Sequence Data MeSH
- Protein Isoforms chemistry genetics metabolism MeSH
- Receptors, Cell Surface genetics metabolism MeSH
- RNA Interference MeSH
- Amino Acid Sequence MeSH
- Signal Transduction * MeSH
- Tribolium growth & development ultrastructure MeSH
- Gene Expression Regulation, Developmental MeSH
- Animals MeSH
- Check Tag
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Insect Proteins MeSH
- Juvenile Hormones MeSH
- RNA, Messenger MeSH
- Protein Isoforms MeSH
- Receptors, Cell Surface MeSH
Metamorphosis of holometabolous insects, an elaborate change of form between larval, pupal and adult stages, offers an ideal system to study the regulation of morphogenetic processes by hormonal signals. Metamorphosis involves growth and differentiation, tissue remodeling and death, all of which are orchestrated by the morphogenesis-promoting ecdysteroids and the antagonistically acting juvenile hormone (JH), whose presence precludes the metamorphic changes. How target tissues interpret this combinatorial effect of the two hormonal cues is poorly understood, mainly because JH does not prevent larval-pupal transformation in the derived Drosophila model, and because the JH receptor is unknown. We have recently used the red flour beetle Tribolium castaneum to show that JH controls entry to metamorphosis via its putative receptor Methoprene-tolerant (Met). Here, we demonstrate that Met mediates JH effects on the expression of the ecdysteroid-response gene Broad-Complex (BR-C). Using RNAi and a classical mutant, we show that Tribolium BR-C is necessary for differentiation of pupal characters. Furthermore, heterochronic combinations of retarded and accelerated phenotypes caused by impaired BR-C function suggest that besides specifying the pupal fate, BR-C operates as a temporal coordinator of hormonally regulated morphogenetic events across epidermal tissues. Similar results were also obtained when using the lacewing Chrysopa perla (Neuroptera), a member of another holometabolous group with a primitive type of metamorphosis. The tissue coordination role of BR-C may therefore be a part of the Holometabola groundplan.
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