Steroid Hormone Inactivation Is Required during the Juvenile-Adult Transition in Drosophila

Kim F. Rewitz, Naoki Yamanaka, Michael B O'Connor

Research output: Contribution to journalArticlepeer-review

60 Scopus citations

Abstract

Steroid hormones are systemic signaling molecules that regulate juvenile-adult transitions in both insects and mammals. In insects, pulses of the steroid hormone 20-hydroxyecdysone (20E) are generated by increased biosynthesis followed by inactivation/clearance. Although mechanisms that control 20E synthesis have received considerable recent attention, the physiological significance of 20E inactivation remains largely unknown. We show that the cytochrome P450 Cyp18a1 lowers 20E titer during the Drosophila prepupal to pupal transition. Furthermore, this reduction of 20E levels is a prerequisite to induce βFTZ-F1, a key factor in the genetic hierarchy that controls early metamorphosis. Resupplying βFTZ-F1 rescues Cyp18a1-deficient prepupae. Because Cyp18a1 is 20E-inducible, it appears that the increased production of steroid is responsible for its eventual decline, thereby generating the regulatory pulse required for proper temporal progression of metamorphosis. The coupling of hormone clearance to βFTZ-F1 expression suggests a general mechanism by which transient signaling drives unidirectional progression through a multistep process.

Original languageEnglish (US)
Pages (from-to)895-902
Number of pages8
JournalDevelopmental Cell
Volume19
Issue number6
DOIs
StatePublished - Dec 14 2010

Bibliographical note

Funding Information:
K.F.R. was supported by a postdoctoral fellowship from The Danish Natural Science Research Council (grant no. 272-07-0340). N.Y. is supported by a postdoctoral fellowship from the Japan Society for the Promotion of Science. M.B.O. was an investigator with the Howard Hughes Medical Institute for a portion of this work. Additional support was provided by NIH R01 GM093301. We are grateful to our collaborators, L. Gilbert, J.T. Warren, and R. Rybczynski for many stimulating discussions. We thank E. Bier for Cyp18a1 lines.

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