scispace - formally typeset
Open AccessJournal ArticleDOI

Induction of translatable mRNA for dopa decarboxylase in Drosophila: an early response to ecdysterone.

TLDR
Exogenous feeding of ecdysterone to these larvae results in a rapid synthesis of dopa decarboxylase in the epidermal cells, which may be a primary response of these target cells to ecdystersone.
Abstract
Ecdysteroid titer and dopa decarboxylase (aromatic-L-amino-acid carboxy-lyase, EC 4.1.1.28) activity were determined throughout the life cycle of Drosophila melanogaster. Five peaks in the amount of hormone were observed, which preceeded five dopa decarboxylase peaks by times ranging from 5 to 58 hr. Late in the third instar the hormone and enzyme maxima are nearly coincident. The increase in enzyme activity observed at this time is paralleled by an increase in translatable dopa decarboxylase mRNA. To obtain evidence that ecdysterone induces the appearance of this mRNA we made use of the temperature-sensitive ecd1 mutant. Garen et al. [Garen, A., Kauvar, L. & Lepesant, J.-A. (1977) Proc. Natl, Acad. Sci. USA 74, 5099-5103] have shown that when third instar mutant larvae are kept at 29 degrees C, the ecdysteroid titer remains low. In such larvae we show that the normal increase in dopa decarboxylase activity fails to appear, and no translatable dopa decarboxylase mRNA can be detected. Exogenous feeding of ecdysterone to these larvae results in a rapid synthesis of dopa decarboxylase in the epidermal cells. In addition, a parallel increase in translatable dopa decarboxylase mRNA occurs, which may be a primary response of these target cells to ecdysterone.

read more

Citations
More filters
Book ChapterDOI

Cellular and Molecular Actions of Juvenile Hormone I. General Considerations and Premetamorphic Actions

TL;DR: This chapter describes the premetamorphic actions and general consideration of cellular and molecular actions of juvenile hormone (JH) and the present understanding of the molecular basis of this action.
Book ChapterDOI

The Genetics Of Biogenic Amine Metabolism, Sclerotization, And Melanization In Drosophila Melanogaster*

TL;DR: The availability of mutations that interrupt biogenic-amine metabolism in an experimentally suitable organism such as Drosophila should provide powerful analytical tools for neurochemists, neurophysiologists, and behavioral biologists.
Journal ArticleDOI

Broad specifies pupal development and mediates the ‘status quo’ action of juvenile hormone on the pupal-adult transformation in Drosophila and Manduca

TL;DR: The 'status quo' action of JH on the pupal-adult transformation is mediated by the JH-induced re-expression of BR, and the BR isoforms during adult development of Drosophila suppressed bristle and hair formation when induced early or redirected cuticle production toward the pupa program when induced late.
Journal ArticleDOI

Phantom encodes the 25-hydroxylase of Drosophila melanogaster and Bombyx mori: a P450 enzyme critical in ecdysone biosynthesis.

TL;DR: The identity of the Drosophila gene phantom (phm), located at 17D1 of the X chromosome, as encoding the microsomal 25-hydroxylase (Cyp306a1) is reported, and in situ developmental gene analysis, in addition to northern, western and RT-PCR techniques, are consistent with this identification.
Journal ArticleDOI

Spatial and temporal patterns of E74 transcription during Drosophila development

TL;DR: The E74 gene occupies one of the early puff loci central to the Ashburner model for the ecdysone-induced puffing pattern in Drosophila, and it is shown that the E74A promoter is directly activated by ecDysone and is subsequently repressed by Ecdys one-induced proteins.
Related Papers (5)