32
Views
10
CrossRef citations to date
0
Altmetric
Original Article

Mutations Affecting the Delayed Rectifier Potassium Current in Drosophila

, &
Pages 107-123 | Received 14 Dec 1999, Published online: 11 Jul 2009
 

Abstract

Mutations and pharmacological agents have been used to resolve and analyze several K+ currents in Drosophila. Mutations that affect channels carrying the voltage-activated IA and the Ca2+-activated ICF have helped greatly in analyzing the structure, function and regulation of these channels. We now report mutations that selectively affect the delayed rectifier current, IR. Flies mutagenized with ethylmethanesulfonate were screened for temperature-induced paralysis. Paralytic mutants identified in the screen were examined for K+ currents in the larval body-wall muscles. The z66 mutant larvae showed a significant reduction in IK. The mutation did not affect other K+ currents (IA, ICF, or ICS) or the Ca2+ channel current in the muscles. Another mutation, z4, which showed reduced IK, failed to complement z66. Genetic analysis localized the gene disrupted by z66 and z4 to the left arm of chromosome 3, in the 63A1–63B6 region on polytene chromosomes. The z66 and the z4 mutations, which lie in the Shab K+ channel gene, provide an opportunity to undertake analysis of the functioning of these channels and to study the role of these channels in membrane excitability.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.