Family ties of gated pores: evolution of the sensor module

ABSTRACT The six‐transmembrane channels are thought to be composed of two modules: pore and sensor. Whereas the modular design of the pore has been established, the modularity of the sensor remains hypothetical. As a first step toward establishing the modularity of this region, we searched for genes...

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Veröffentlicht in:The FASEB journal 2002-10, Vol.16 (12), p.1623-1629
Hauptverfasser: Kuma'novics, Attila, Levin, Gal, Blount, Paul
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container_title The FASEB journal
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creator Kuma'novics, Attila
Levin, Gal
Blount, Paul
description ABSTRACT The six‐transmembrane channels are thought to be composed of two modules: pore and sensor. Whereas the modular design of the pore has been established, the modularity of the sensor remains hypothetical. As a first step toward establishing the modularity of this region, we searched for genes where the sensor is found independent of the pore and have identified new members of the sensor superfamily. Analysis of these sensors reveals a motif shared among not only these newly discovered members and voltage‐gated, transient receptor potential, and polycystin channel sensors, but also MscL, a bacterial mechanosensitive channel. Mutational analyses presented here and in previous studies demonstrate that highly conserved residues within this motif are required for normal channel activity; mutations of residues within this motif in different subfamilies lead to consistent channel phenotypes. Previous studies have demonstrated that peptides containing this motif and the adjacent conserved transmembrane domain elicit channel activities when reconstituted into lipid membranes. These data provide evidence for the modularity of the sensor, imply a model for its evolution, suggest a common origin for mechano‐and voltage‐sensing, and may offer a glimpse of the properties of the first sensor/channel.—Kumánovics, A., Levin, G., Blount, P. Family ties of gated pores: evolution of the sensor module. FASEB J. 16, 1623–1629 (2002)
doi_str_mv 10.1096/fj.02-0238hyp
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source MEDLINE; Wiley Online Library Journals Frontfile Complete; Alma/SFX Local Collection
subjects Amino Acid Sequence
Animals
Bacterial Proteins - chemistry
Bacterial Proteins - genetics
Bacterial Proteins - physiology
Evolution, Molecular
Humans
Ion Channel Gating - physiology
Ion Channels - chemistry
Ion Channels - genetics
Ion Channels - physiology
Mechanotransduction, Cellular - physiology
Models, Molecular
Molecular Sequence Data
MscL
Sequence Homology, Amino Acid
TPTE
transient receptor potential
tyrosine phosphatases
voltage‐gated channel
title Family ties of gated pores: evolution of the sensor module
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