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Potassium translocation in plants is accomplished by a large variety of transport systems. Most of the available molecular information on these proteins concerns voltage-gated potassium channels (Kv channels). The Arabidopsis genome comprises nine genes encoding alpha-subunits of Kv channels. Based on knowledge of their animal homologues, and on biochemical investigations, it is broadly admitted that four such polypeptides must assemble to yield a functional Kv channel. The intrinsic functional properties of Kv channel alpha-subunits have been described by expressing them in suitable heterologous contexts where homo-tetrameric channels could be characterized. However, due to the high similarity of both the polypeptidic sequence and the structural scheme of Kv channel alpha-subunits, formation of heteromeric Kv channels by at least two types of alpha-subunits is conceivable. Several examples of such heteromeric plant Kv channels have been studied in heterologous expression systems and evidence that heteromerization actually occurs in planta has now been published. It is therefore challenging to uncover the physiological role of this heteromerization. Fine tuning of Kv channels by heteromerisation could be relevant not only to potassium transport but also to electrical signaling within the plant.
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http://dx.doi.org/10.4161/psb.3.9.6209 | DOI Listing |
bioRxiv
August 2025
Department of Biological Sciences, Southern Methodist University, Dallas, TX.
The leading cause of epilepsy-related mortality is sudden unexpected death in epilepsy (SUDEP), resulting from seizure-induced cardiorespiratory arrest by mechanisms that remain unresolved. Mutations in ion channel genes expressed in both brain and heart represent SUDEP risk factors because they can disrupt neural and cardiac rhythms, providing a unified explanation for seizures and lethal arrhythmias. However, the relative contributions of brain-driven mechanisms, heart-intrinsic processes, and seizures to cardiac dysfunction in epilepsy remain unclear.
View Article and Find Full Text PDFEuropace
August 2025
Translational Cardiology, Institute of Physiology and Department of Cardiology, University of Bern, Switzerland.
Background And Aims: Loss-of-function mutations in KCNQ1 and KCNH2 (α-subunits of the slow delayed IKs and rapid delayed IKr-conducting repolarising K+ channels) lead to long QT syndrome type 1 (LQT1) and 2 (LQT2), respectively. These channelopathies present with longer action potential duration (APD) and prolonged QT interval on ECG, which can ultimately lead to deadly arrhythmias. Here we investigated the therapeutic potential of the polyunsaturated fatty acid docosahexaenoyl glycine (DHA-gly) in normalizing APD and QT interval in LQT2 by increasing IKs.
View Article and Find Full Text PDFChannels (Austin)
December 2025
Department of Physiology, University of Maryland School of Medicine, Baltimore, MD, USA.
Seventy-five unique variants in the gene have been identified from individuals with neurological disorders. However, variant pathogenicity and evidence for disease causality are lacking in most cases. In this study, the variants N999S and E656A (rs886039469 and rs149000684, respectively) were investigated from two individuals presenting with neurological disorders.
View Article and Find Full Text PDFEur J Pharmacol
October 2025
Department of Cardiovascular Medicine of the First Affiliated Hospital of Bengbu Medical University, Bengbu, Anhui, 233000, PR China; Key Laboratory of Basic and Clinical Cardiovascular and Cerebrovascular Diseases, Bengbu Medical University, Bengbu, Anhui Province, 233004, PR China. Electronic addr
Salidroside (Sal) is a natural active ingredient extracted from Crassulaceae plants, which has pharmacological effects such as anti-tumor, anti-oxidation, and cardiovascular protection. Potassium channel function in pulmonary artery smooth muscle cells (PASMCs) is crucial in the development of pulmonary arterial hypertension (PAH). This study explored the effects of Sal on large-conductance calcium-activated potassium channels (BKCa) in these cells, focusing on the mechanisms underlying its protective effect in PAH.
View Article and Find Full Text PDFBiochem Genet
July 2025
Laboratory of Anesthesia and Critical Care Medicine, National-Local Joint Engineering Research Centre of Translational Medicine of Anesthesiology, West China Hospital, Sichuan University, Chengdu, Sichuan, China.
The KCNE gene family is crucial for physiological and pathological processes in the body and encodes small transmembrane proteins that function as auxiliary subunits to regulate voltage-gated potassium channels (K channels). This family includes five members, KCNE1, KCNE2, KCNE3, KCNE4, and KCNE5, whose encoded proteins are referred to as MinK and MinK-related peptides (MiRPs), which influence the properties and localization of K. When KCNE is coexpressed with Kv, it can alter the conductance, gating kinetics, and pharmacology of the channel.
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