Broad-Complex acts downstream of Met in juvenile hormone signaling to coordinate primitive holometabolan metamorphosis
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
18171683
DOI
10.1242/dev.016097
PII: dev.016097
Knihovny.cz E-zdroje
- MeSH
- biologická proměna * MeSH
- biologické modely MeSH
- brouci růst a vývoj metabolismus ultrastruktura MeSH
- hmyzí proteiny chemie genetika metabolismus MeSH
- juvenilní hormony metabolismus MeSH
- konzervovaná sekvence MeSH
- kukla ultrastruktura MeSH
- larva ultrastruktura MeSH
- messenger RNA genetika metabolismus MeSH
- molekulární sekvence - údaje MeSH
- protein - isoformy chemie genetika metabolismus MeSH
- receptory buněčného povrchu genetika metabolismus MeSH
- RNA interference MeSH
- sekvence aminokyselin MeSH
- signální transdukce * MeSH
- Tribolium růst a vývoj ultrastruktura MeSH
- vývojová regulace genové exprese MeSH
- zvířata MeSH
- Check Tag
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- hmyzí proteiny MeSH
- juvenilní hormony MeSH
- messenger RNA MeSH
- protein - isoformy MeSH
- receptory buněčného povrchu 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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