AI Article Synopsis

  • A large number of potassium channels are conserved through evolution, but their functions in living organisms are not well understood.
  • The study focuses on the tobacco hornworm, Manduca sexta, which serves as an effective model to analyze specific neurons involved in simple behaviors and hormonal regulation during metamorphosis.
  • The researchers successfully cloned a potassium channel called Manduca sexta ether à-go-go (Mseag), demonstrating its voltage-dependent properties and suggesting its expression is influenced by steroid hormones during development.

Article Abstract

A very large number of evolutionarily conserved potassium channels have been identified but very little is known about their function or modulation in vivo. Metamorphosis of the tobacco hornworm, Manduca sexta, is a compelling model system for such studies because it permits analysis to be conducted at the level of identified neurons whose roles in simple behaviors and endocrine regulation are known. We present here the characterization of the first ion channel to be cloned from this animal. Partial genomic sequence for Manduca sexta ether à-go-go (Mseag) and a cDNA clone encoding the Mseag open reading frame were obtained. Genomic Southern analysis indicates that Manduca contains a single member of the eag subfamily per haploid genome. When expressed in Xenopus oocytes, MsEag channels conduct a voltage-dependent, K+ selective outward current with an inactivating component that closely resembles the Drosophila eag current. Mseag transcripts were restricted to the nervous system, adult antenna, and one set of larval skeletal muscles. Steroid hormonal regulation of Mseag expression is suggested by the temporal correlation of developmental changes in transcript expression with the changing steroid titers that promote metamorphosis. These results provide the foundation for functional and modulatory studies of the Eag family of K+ channels in Manduca, which will complement the genetic analysis in Drosophila.

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Source
http://dx.doi.org/10.1002/neu.10188DOI Listing

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