Golgi anti-apoptotic protein: a tale of camels, calcium, channels and cancer

Bibliographic Details
Title: Golgi anti-apoptotic protein: a tale of camels, calcium, channels and cancer
Authors: Guia Carrara, Maddy Parsons, Nuno Saraiva, Geoffrey L. Smith
Source: Open Biology, Vol 7, Iss 5 (2017)
Publisher Information: The Royal Society, 2017.
Publication Year: 2017
Collection: LCC:Biology (General)
Subject Terms: golgi anti-apoptotic protein, ion channel, calcium flux, cell adhesion and migration, bax inhibitor-1, tmbim, Biology (General), QH301-705.5
More Details: Golgi anti-apoptotic protein (GAAP), also known as transmembrane Bax inhibitor-1 motif-containing 4 (TMBIM4) or Lifeguard 4 (Lfg4), shares remarkable amino acid conservation with orthologues throughout eukaryotes, prokaryotes and some orthopoxviruses, suggesting a highly conserved function. GAAPs regulate Ca2+ levels and fluxes from the Golgi and endoplasmic reticulum, confer resistance to a broad range of apoptotic stimuli, promote cell adhesion and migration via the activation of store-operated Ca2+ entry, are essential for the viability of human cells, and affect orthopoxvirus virulence. GAAPs are oligomeric, multi-transmembrane proteins that are resident in Golgi membranes and form cation-selective ion channels that may explain the multiple functions of these proteins. Residues contributing to the ion-conducting pore have been defined and provide the first clues about the mechanistic link between these very different functions of GAAP. Although GAAPs are naturally oligomeric, they can also function as monomers, a feature that distinguishes them from other virus-encoded ion channels that must oligomerize for function. This review summarizes the known functions of GAAPs and discusses their potential importance in disease.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2046-2441
Relation: https://doaj.org/toc/2046-2441
DOI: 10.1098/rsob.170045
Access URL: https://doaj.org/article/512676182fc447bda4eedafbf773aa8c
Accession Number: edsdoj.512676182fc447bda4eedafbf773aa8c
Database: Directory of Open Access Journals
More Details
ISSN:20462441
DOI:10.1098/rsob.170045
Published in:Open Biology
Language:English