K+ currents inDrosophila muscles have been resolved into two voltage-activated currents (I A andI K) and two Ca2+-activated currents (I CF and I CS). Mutations that affect IA (Shaker) andI CF (slowpoke) have helped greatly in the analysis of these currents and their role in membrane excitability. Lack of mutations that specifically affect channels for the delayed rectifier current (I K) has made their genetic and functional identity difficult to elucidate. With the help of mutations in the Shab K+ channel gene, we show that this gene encodes the delayed rectifier K+channels in Drosophila. Three mutant alleles with a temperature-sensitive paralytic phenotype were analyzed. Analysis of the ionic currents from mutant larval body wall muscles showed a specific effect on delayed rectifier K+ current (I K). Two of the mutant alleles contain missense mutations, one in the amino-terminal region of the channel protein and the other in the pore region of the channel. The third allele contains two deletions in the amino-terminal region and is a null allele. These observations identity the channels that carry the delayed rectifier current and provide an in vivophysiological role for the Shab-encoded K+channels in Drosophila. The availability of mutations that affect I K opens up possibilities for studyingI K and its role in larval muscle excitability.
Mutational Analysis of the Shab-encoded Delayed Rectifier K+ Channels in Drosophila *
Priti Hegde,Gang-Gou Gu,Dong Chen,S. Free,Satpal Singh
Published 1999 in Journal of Biological Chemistry
ABSTRACT
PUBLICATION RECORD
- Publication year
1999
- Venue
Journal of Biological Chemistry
- Publication date
1999-07-30
- Fields of study
Biology, Medicine
- Identifiers
- External record
- Source metadata
Semantic Scholar, PubMed
CITATION MAP
EXTRACTION MAP
CLAIMS
- No claims are published for this paper.
CONCEPTS
- No concepts are published for this paper.
REFERENCES
Showing 1-48 of 48 references · Page 1 of 1
CITED BY
Showing 1-30 of 30 citing papers · Page 1 of 1