Journal article
The Drosophila gene CheB42a is a novel modifier of Deg/ENaC channel function
PloS one, Vol.5(2), pp.e9395-e9395
02/24/2010
DOI: 10.1371/journal.pone.0009395
PMCID: PMC2827562
PMID: 20195381
Abstract
Degenerin/epithelial Na(+) channels (DEG/ENaC) represent a diverse family of voltage-insensitive cation channels whose functions include Na(+) transport across epithelia, mechanosensation, nociception, salt sensing, modification of neurotransmission, and detecting the neurotransmitter FMRFamide. We previously showed that the Drosophila melanogaster Deg/ENaC gene lounge lizard (llz) is co-transcribed in an operon-like locus with another gene of unknown function, CheB42a. Because operons often encode proteins in the same biochemical or physiological pathway, we hypothesized that CHEB42A and LLZ might function together. Consistent with this hypothesis, we found both genes expressed in cells previously implicated in sensory functions during male courtship. Furthermore, when coexpressed, LLZ coprecipitated with CHEB42A, suggesting that the two proteins form a complex. Although LLZ expressed either alone or with CHEB42A did not generate ion channel currents, CHEB42A increased current amplitude of another DEG/ENaC protein whose ligand (protons) is known, acid-sensing ion channel 1a (ASIC1a). We also found that CHEB42A was cleaved to generate a secreted protein, suggesting that CHEB42A may play an important role in the extracellular space. These data suggest that CHEB42A is a modulatory subunit for sensory-related Deg/ENaC signaling. These results are consistent with operon-like transcription of CheB42a and llz and explain the similar contributions of these genes to courtship behavior.
Details
- Title: Subtitle
- The Drosophila gene CheB42a is a novel modifier of Deg/ENaC channel function
- Creators
- Yehuda Ben-Shahar - Howard Hughes Medical Institute, Chevy Chase, Maryland, United States of AmericaBeika LuDaniel M CollierPeter M SnyderMikael SchnizlerMichael J Welsh
- Resource Type
- Journal article
- Publication Details
- PloS one, Vol.5(2), pp.e9395-e9395
- DOI
- 10.1371/journal.pone.0009395
- PMID
- 20195381
- PMCID
- PMC2827562
- NLM abbreviation
- PLoS One
- ISSN
- 1932-6203
- eISSN
- 1932-6203
- Publisher
- Public Library of Science; United States
- Grant note
- Howard Hughes Medical Institute P30 DK054759 / NIDDK NIH HHS R03 DC010244 / NIDCD NIH HHS DK54759 / NIDDK NIH HHS
- Language
- English
- Date published
- 02/24/2010
- Academic Unit
- Neurology; Molecular Physiology and Biophysics; Pulmonary, Critical Care, and Occupational Medicine; Cardiovascular Medicine; Neurosurgery; Medicine Administration; Internal Medicine
- Record Identifier
- 9984017737302771
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