The Enigmatic Cytoplasmic Regions of KCNH Channels. Issue 1 (16th January 2015)
- Record Type:
- Journal Article
- Title:
- The Enigmatic Cytoplasmic Regions of KCNH Channels. Issue 1 (16th January 2015)
- Main Title:
- The Enigmatic Cytoplasmic Regions of KCNH Channels
- Authors:
- Morais-Cabral, João H.
Robertson, Gail A. - Abstract:
- Abstract: KCNH channels are expressed across a vast phylogenetic and evolutionary spectrum. In humans, they function in a wide range of tissues and serve as biomarkers and targets for diseases such as cancer and cardiac arrhythmias. These channels share a general architecture with other voltage-gated ion channels but are distinguished by the presence of an N-terminal PAS ( P er- A rnt- S im) domain and a C-terminal domain with homology to cyclic nucleotide binding domains (referred to as the CNBh domain). Cytosolic regions outside these domains show little conservation between KCNH families but are strongly conserved across species within a family, likely reflecting variability that confers specificity to individual channel types. PAS and CNBh domains participate in channel gating, but at least twice in evolutionary history, the PAS domain has been lost and it is omitted by alternate transcription to create a distinct channel subunit in one family. In this focused review, we present current knowledge of the structure and function of these cytosolic regions, discuss their evolution as modular domains and provide our perspective on the important questions moving forward. Graphical abstract: Highlights: Aberrant KCNH function is associated with cardiac arrhythmia, epilepsy and cancer. Structural and functional studies show that PAS and CNBh domains interact. Disruption of PAS or CNBh domain alters channel gating. PAS domains are absent in some lineages and in some KCNH subunitAbstract: KCNH channels are expressed across a vast phylogenetic and evolutionary spectrum. In humans, they function in a wide range of tissues and serve as biomarkers and targets for diseases such as cancer and cardiac arrhythmias. These channels share a general architecture with other voltage-gated ion channels but are distinguished by the presence of an N-terminal PAS ( P er- A rnt- S im) domain and a C-terminal domain with homology to cyclic nucleotide binding domains (referred to as the CNBh domain). Cytosolic regions outside these domains show little conservation between KCNH families but are strongly conserved across species within a family, likely reflecting variability that confers specificity to individual channel types. PAS and CNBh domains participate in channel gating, but at least twice in evolutionary history, the PAS domain has been lost and it is omitted by alternate transcription to create a distinct channel subunit in one family. In this focused review, we present current knowledge of the structure and function of these cytosolic regions, discuss their evolution as modular domains and provide our perspective on the important questions moving forward. Graphical abstract: Highlights: Aberrant KCNH function is associated with cardiac arrhythmia, epilepsy and cancer. Structural and functional studies show that PAS and CNBh domains interact. Disruption of PAS or CNBh domain alters channel gating. PAS domains are absent in some lineages and in some KCNH subunit isoforms. Functional roles of KCNH cytoplasmic domains remain elusive. … (more)
- Is Part Of:
- Journal of molecular biology. Volume 427:Issue 1(2015:Jan. 01)
- Journal:
- Journal of molecular biology
- Issue:
- Volume 427:Issue 1(2015:Jan. 01)
- Issue Display:
- Volume 427, Issue 1 (2015)
- Year:
- 2015
- Volume:
- 427
- Issue:
- 1
- Issue Sort Value:
- 2015-0427-0001-0000
- Page Start:
- 67
- Page End:
- 76
- Publication Date:
- 2015-01-16
- Subjects:
- KCNH -- PAS -- potassium channels -- ether-à-go-go -- CNBh domains
Molecular biology -- Periodicals
Biology -- Periodicals
Biochemistry -- Periodicals
Bacteriology -- Periodicals
Molecular Biology -- Periodicals
Biochemistry -- Periodicals
Biologie moléculaire -- Périodiques
Biologie -- Périodiques
Biochimie -- Périodiques
Moleculaire biologie
Biochemistry
Biology
Molecular biology
Periodicals
572.805 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00222836 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.jmb.2014.08.008 ↗
- Languages:
- English
- ISSNs:
- 0022-2836
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5020.700000
British Library DSC - BLDSS-3PM
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- 21113.xml