TY - JOUR
T1 - Formation and dissociation of proteasome storage granules are regulated by cytosolic pH
AU - Peters Lee Zeev, Z.
AU - Hazan, Rotem
AU - Breker, Michal
AU - Schuldiner, Maya
AU - Ben-Aroya, Shay
N1 - Human Frontier Science Program career development award [00005/2010]; Israeli Cancer Research Fund career development [2011-713]; European Research Council [26039]The work was supported in part by Human Frontier Science Program career development award grant (career development award 00005/2010) and Israeli Cancer Research Fund career development grant (research career development award 2011-713) to S. Ben-Aroya. M. Schuldiner was funded by a European Research Council grant (starting grant 26039).
PY - 2013/5/27
Y1 - 2013/5/27
N2 - The 26S proteasome is the major protein degradation machinery of the cell and is regulated at many levels. One mode of regulation involves accumulation of proteasomes in proteasome storage granules (PSGs) upon glucose depletion. Using a systematic robotic screening approach in yeast, we identify trans-acting proteins that regulate the accumulation of proteasomes in PSGs. Our dataset was enriched for subunits of the vacuolar adenosine triphosphatase (V-ATPase) complex, a proton pump required for vacuole acidification. We show that the impaired ability of V-ATPase mutants to properly govern intracellular pH affects the kinetics of PSG formation. We further show that formation of other protein aggregates upon carbon depletion also is triggered in mutants with impaired activity of the plasma membrane proton pump and the V-ATPase complex. We thus identify cytosolic pH as a specific cellular signal involved both in the glucose sensing that mediates PSG formation and in a more general mechanism for signaling carbon source exhaustion.
AB - The 26S proteasome is the major protein degradation machinery of the cell and is regulated at many levels. One mode of regulation involves accumulation of proteasomes in proteasome storage granules (PSGs) upon glucose depletion. Using a systematic robotic screening approach in yeast, we identify trans-acting proteins that regulate the accumulation of proteasomes in PSGs. Our dataset was enriched for subunits of the vacuolar adenosine triphosphatase (V-ATPase) complex, a proton pump required for vacuole acidification. We show that the impaired ability of V-ATPase mutants to properly govern intracellular pH affects the kinetics of PSG formation. We further show that formation of other protein aggregates upon carbon depletion also is triggered in mutants with impaired activity of the plasma membrane proton pump and the V-ATPase complex. We thus identify cytosolic pH as a specific cellular signal involved both in the glucose sensing that mediates PSG formation and in a more general mechanism for signaling carbon source exhaustion.
UR - http://www.scopus.com/inward/record.url?scp=84878560423&partnerID=8YFLogxK
U2 - 10.1083/jcb.201211146
DO - 10.1083/jcb.201211146
M3 - مقالة
C2 - 23690178
SN - 0021-9525
VL - 201
SP - 663
EP - 671
JO - Journal of Cell Biology
JF - Journal of Cell Biology
IS - 5
ER -