PUBLICATION
Zebrafish acid-sensing ion channel (ASIC) 4: Characterization of homo- and heteromeric channels and identification of regions important for activation by H+
- Authors
- Chen, X., Polleichtner, G., Kadurin, I., and Grunder, S.
- ID
- ZDB-PUB-070813-24
- Date
- 2007
- Source
- The Journal of biological chemistry 282(42): 30406-30413 (Journal)
- Registered Authors
- Keywords
- none
- MeSH Terms
-
- Acid Sensing Ion Channels
- Animals
- Dimerization
- Female
- Gene Expression
- Ion Channel Gating/physiology*
- Membrane Proteins/genetics
- Membrane Proteins/metabolism*
- Models, Biological
- Multigene Family
- Nerve Tissue Proteins/genetics
- Nerve Tissue Proteins/metabolism*
- Neurons/metabolism*
- Protein Structure, Tertiary/physiology
- Protons*
- Sodium Channels/genetics
- Sodium Channels/metabolism*
- Xenopus laevis
- Zebrafish/genetics
- Zebrafish/metabolism*
- Zebrafish Proteins/genetics
- Zebrafish Proteins/metabolism*
- PubMed
- 17686779 Full text @ J. Biol. Chem.
Citation
Chen, X., Polleichtner, G., Kadurin, I., and Grunder, S. (2007) Zebrafish acid-sensing ion channel (ASIC) 4: Characterization of homo- and heteromeric channels and identification of regions important for activation by H+. The Journal of biological chemistry. 282(42):30406-30413.
Abstract
There are four genes for Acid-Sensing Ion Channels (ASICs) in the genome of mammalian species. Whereas ASIC1 to ASIC3 form functional H+-gated Na+ channels, ASIC4 is not gated by H+ and its function is unknown. Zebrafish has two ASIC4 paralogs: zASIC4.1 and zASIC4.2. Whereas zASIC4.1 is gated by extracellular H+, zASIC4.2 is not. This differential response to H+ makes zASIC4 paralogs a good model to study the properties of this ion channel. In this study, we found that surface expression of homomeric zASIC4.2 is higher than that of zASIC4.1. Surface expression of zASIC4.1 was much increased by formation of heteromeric channels, suggesting that zASIC4.1 contributes to heteromeric ASICs in zebrafish neurons. Robust surface expression of H+-insensitive zASIC4.2 suggests that zASIC4.2 functions as a homomer and is gated by an as yet unknown stimulus, different from H+. Moreover, we identified a small region just distal to the first transmembrane domain that is crucial for the differential H+ response of the two paralogs. This post-TM1 domain may have a general role in gating of members of this gene family.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping