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SUMOylation and calcium signalling: potential roles in the brain and beyond
Author(s) -
Letícia Coelho-Silva,
Gary J. Stephens,
Helena Cimarosti
Publication year - 2017
Publication title -
neuronal signaling
Language(s) - English
Resource type - Journals
ISSN - 2059-6553
DOI - 10.1042/ns20160010
Subject(s) - sumo protein , microbiology and biotechnology , endoplasmic reticulum , calcium signaling , biology , extracellular , neurotransmission , proteome , second messenger system , neuroscience , chemistry , intracellular , ubiquitin , biochemistry , receptor , gene
Small ubiquitin-like modifier (SUMO) conjugation (or SUMOylation) is a post-translational protein modification implicated in alterations to protein expression, localization and function. Despite a number of nuclear roles for SUMO being well characterized, this process has only started to be explored in relation to membrane proteins, such as ion channels. Calcium ion (Ca 2+ ) signalling is crucial for the normal functioning of cells and is also involved in the pathophysiological mechanisms underlying relevant neurological and cardiovascular diseases. Intracellular Ca 2+ levels are tightly regulated; at rest, most Ca 2+ is retained in organelles, such as the sarcoplasmic reticulum, or in the extracellular space, whereas depolarization triggers a series of events leading to Ca 2+ entry, followed by extrusion and reuptake. The mechanisms that maintain Ca 2+ homoeostasis are candidates for modulation at the post-translational level. Here, we review the effects of protein SUMOylation, including Ca 2+ channels, their proteome and other proteins associated with Ca 2+ signalling, on vital cellular functions, such as neurotransmission within the central nervous system (CNS) and in additional systems, most prominently here, in the cardiac system.

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