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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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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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)</description><identifier>ISSN: 0892-6638</identifier><identifier>EISSN: 1530-6860</identifier><identifier>DOI: 10.1096/fj.02-0238hyp</identifier><identifier>PMID: 12374785</identifier><language>eng</language><publisher>United States</publisher><subject>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</subject><ispartof>The FASEB journal, 2002-10, Vol.16 (12), p.1623-1629</ispartof><rights>FASEB</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c438P-fa822475e63642dad2f94c5cd2cca711ee9c04210df357e257efc81dae3fa90a3</citedby><cites>FETCH-LOGICAL-c438P-fa822475e63642dad2f94c5cd2cca711ee9c04210df357e257efc81dae3fa90a3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1096%2Ffj.02-0238hyp$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1096%2Ffj.02-0238hyp$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12374785$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kuma'novics, Attila</creatorcontrib><creatorcontrib>Levin, Gal</creatorcontrib><creatorcontrib>Blount, Paul</creatorcontrib><title>Family ties of gated pores: evolution of the sensor module</title><title>The FASEB journal</title><addtitle>FASEB J</addtitle><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. 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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)</abstract><cop>United States</cop><pmid>12374785</pmid><doi>10.1096/fj.02-0238hyp</doi><tpages>7</tpages></addata></record> |
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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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