2001
DOI: 10.1016/s0022-1910(01)00063-4
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Vitellogenesis in diapausing and mutant Drosophila melanogaster: further evidence for the relative roles of ecdysteroids and juvenile hormones

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Cited by 96 publications
(59 citation statements)
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“…Also, cpo is highly expressed in the ring gland (29), the primary endocrine structure in Drosophila; this is particularly interesting because diapause is under neuroendocrine control. We also identified a series of cpo ecdysone response elements, suggesting that the effects of cpo on diapause in D. melanogaster may be mediated by ecdysteroids (30). Loss-of-function cpo mutations are lethal, and partial loss-offunction mutations generate a variety of behavioral phenotypes (23) and neurological abnormalities (31).…”
Section: Discussionmentioning
confidence: 94%
“…Also, cpo is highly expressed in the ring gland (29), the primary endocrine structure in Drosophila; this is particularly interesting because diapause is under neuroendocrine control. We also identified a series of cpo ecdysone response elements, suggesting that the effects of cpo on diapause in D. melanogaster may be mediated by ecdysteroids (30). Loss-of-function cpo mutations are lethal, and partial loss-offunction mutations generate a variety of behavioral phenotypes (23) and neurological abnormalities (31).…”
Section: Discussionmentioning
confidence: 94%
“…Exogenous application of juvenile hormone analogs also breaks diapause, and the diapause response is associated with a reduced rate of juvenile hormone synthesis in the corpora allata ). Studies by Richard et al (1998Richard et al ( , 2001) also implicated a role for ecdysteroids in mediating vitello- genesis and the diapause response and further supported that D. melanogaster diapause is under neuroendocrine control. The expression of diapause was shown to vary both among laboratory strains and natural populations (Williams and Sokolowski 1993).…”
Section: Variance For the Diapause Phenotypementioning
confidence: 91%
“…During the reproductive phase of the fruit-fly, JH controls the early synthesis of yolk proteins (YPs) by the fat bodies and the ovarian follicle cells, and YPs are taken up by the developing egg chambers. JH also induces the ovaries to produce 20-hydroxyecdysone (20-OH Ecd), which sustains late vitellogenesis, by inducing the synthesis and uptake of YPs by the fat bodies [72][73][74][75]. However, an excess of 20-OH Ecd induces apoptosis in nurse cells of stage 9 egg chambers, during early vitellogenesis.…”
Section: Larval and Adult Diapause Are Regulated By Jh And Ecdmentioning
confidence: 99%