TY - JOUR
T1 - The GET Complex Mediates Insertion of Tail-Anchored Proteins into the ER Membrane
AU - Schuldiner, Maya
AU - Metz, Jutta
AU - Schmid, Volker
AU - Denic, Vladimir
AU - Rakwalska, Magdalena
AU - Schmitt, Hans Dieter
AU - Schwappach, Blanche
AU - Weissman, Jonathan S.
PY - 2008/8/22
Y1 - 2008/8/22
N2 - Tail-anchored (TA) proteins, defined by the presence of a single C-terminal transmembrane domain (TMD), play critical roles throughout the secretory pathway and in mitochondria, yet the machinery responsible for their proper membrane insertion remains poorly characterized. Here we show that Get3, the yeast homolog of the TA-interacting factor Asna1/Trc40, specifically recognizes TMDs of TA proteins destined for the secretory pathway. Get3 recognition represents a key decision step, whose loss can lead to misinsertion of TA proteins into mitochondria. Get3-TA protein complexes are recruited for endoplasmic reticulum (ER) membrane insertion by the Get1/Get2 receptor. In vivo, the absence of Get1/Get2 leads to cytosolic aggregation of Get3-TA complexes and broad defects in TA protein biogenesis. In vitro reconstitution demonstrates that the Get proteins directly mediate insertion of newly synthesized TA proteins into ER membranes. Thus, the GET complex represents a critical mechanism for ensuring efficient and accurate targeting of TA proteins. © 2008 Elsevier Inc. All rights reserved.
AB - Tail-anchored (TA) proteins, defined by the presence of a single C-terminal transmembrane domain (TMD), play critical roles throughout the secretory pathway and in mitochondria, yet the machinery responsible for their proper membrane insertion remains poorly characterized. Here we show that Get3, the yeast homolog of the TA-interacting factor Asna1/Trc40, specifically recognizes TMDs of TA proteins destined for the secretory pathway. Get3 recognition represents a key decision step, whose loss can lead to misinsertion of TA proteins into mitochondria. Get3-TA protein complexes are recruited for endoplasmic reticulum (ER) membrane insertion by the Get1/Get2 receptor. In vivo, the absence of Get1/Get2 leads to cytosolic aggregation of Get3-TA complexes and broad defects in TA protein biogenesis. In vitro reconstitution demonstrates that the Get proteins directly mediate insertion of newly synthesized TA proteins into ER membranes. Thus, the GET complex represents a critical mechanism for ensuring efficient and accurate targeting of TA proteins. © 2008 Elsevier Inc. All rights reserved.
KW - CELLBIO
KW - PROTEINS
U2 - 10.1016/j.cell.2008.06.025
DO - 10.1016/j.cell.2008.06.025
M3 - Article
SN - 1097-4172
VL - 134
SP - 634
EP - 645
JO - Cell
JF - Cell
IS - 4
ER -