RNA interference-mediated knockdown of a GATA factor reveals a link to anautogeny in the mosquito Aedes aegypti

  1. Geoffrey M. Attardo*,,
  2. Stephen Higgs,
  3. Kimberley A. Klingler,
  4. Dana L. Vanlandingham, and
  5. Alexander S. Raikhel*,§
  1. *Department of Entomology, University of California, Riverside, CA 92521; Graduate Program in Genetics, Michigan State University, East Lansing, MI 48824; and University of Texas Medical Branch, Galveston, TX 77555
  1. Communicated by John H. Law, University of Arizona, Tucson, AZ, September 3, 2003 (received for review April 29, 2003)

Abstract

Blood feeding tightly regulates the reproductive cycle in anautogenous mosquitoes. Vitellogenesis (the synthesis of yolk protein precursors) is a key event in the mosquito reproductive cycle and is activated in response to a blood meal. Before blood feeding, Aedes aegypti is in a state of reproductive arrest during which the yolk protein precursor genes (YPPs) are repressed. The regulatory region of the major YPP gene vitellogenin (Vg) has multiple GATA-binding sites required for the high expression level of this gene. However, a GATA factor (AaGATAr) likely acts as a repressor, preventing activation of this gene before a blood meal. Here we report in vivo data confirming the role of AaGATAr as a repressor of the Vg gene at the state of previtellogenic arrest. Using an RNA interference (RNAi)-mediated technique in conjunction with the Sindbis viral expression system, we show that knockdown of the AaGATAr gene results in an increased basal level of expression of the Vg gene and an elevated response to the steroid hormone 20-hydroxyecdysone in mosquitoes in a state of arrest. These experiments have revealed a component in the molecular mechanism by which anautogeny is maintained in A. aegypti.

Footnotes

  • § To whom correspondence should be addressed. E-mail: alexander.raikhel{at}ucr.edu.

  • Abbreviations: Vg, vitellogenin; 20E, 20-hydroxyecdysone; EcR, ecdysone receptor; USP, Ultraspiracle; YPP, yolk protein precursor; RNAi, RNA interference.

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