Sexual dimorphism of diapause regulation in the hemipteran bug Pyrrhocoris apterus
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
35007710
DOI
10.1016/j.ibmb.2022.103721
PII: S0965-1748(22)00003-0
Knihovny.cz E-zdroje
- Klíčová slova
- Allatectomy, Corpus allatum, Juvenile hormone, Mating, Methoprene-tolerant, Photoperiod, Reproductive diapause, Seasonality, Taiman,
- MeSH
- corpora allata MeSH
- diapauza hmyzu * MeSH
- diapauza * MeSH
- Heteroptera * fyziologie MeSH
- juvenilní hormony MeSH
- methopren MeSH
- pohlavní dimorfismus MeSH
- rozmnožování MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- juvenilní hormony MeSH
- methopren MeSH
Diapause is one of the major strategies for insects to prepare for and survive harsh seasons. In females, the absence of juvenile hormone (JH) is a hallmark of adult reproductive diapause, a developmental arrest, which is much less characterized in males. Here we show that juvenile hormone III skipped bisepoxide (JHSB3) titers in hemolymph remarkably differ between reproductive males and females of the linden bug Pyrrhocoris apterus, whereas no JH was detected in diapausing adults of both sexes. Like in females, ectopic application of JH mimic effectively terminated male diapause through the canonical JH receptor components, Methoprene-tolerant and Taiman. In contrast to females, long photoperiod induced reproduction even in males with silenced JH reception or in males with removed corpus allatum (CA), the JH-producing gland. JHSB3 was detected in the accessory glands (MAG) of reproductive males, unexpectedly, even in males without CA. If there is a source of JHSB3 outside CA or a long-term storage of JHSB3 in MAGs remains to be elucidated. These sex-related idiosyncrasies are further manifested in different dynamics of diapause termination in P. apterus by low temperature. We would like to propose that this sexual dimorphism of diapause regulation might be explained by the different reproductive costs for each sex.
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