Sec16 influences transitional ER sites by regulating rather than organizing COPII.
Sec16 influences transitional ER sites by regulating rather than organizing COPII.
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DOI:
10.1091/mbc.e13-04-0185
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发表时间:
2013-11
影响因子:
3.3
通讯作者:
Glick BS
中科院分区:
文献类型:
--
作者:
Bharucha N;Liu Y;Papanikou E;McMahon C;Esaki M;Jeffrey PD;Hughson FM;Glick BS
It has been proposed that during the budding of COPII vesicles from transitional ER (tER) sites, Sec16 plays two distinct roles: negatively regulating COPII turnover and organizing COPII assembly. New data suggest that Sec16 does not in fact organize COPII and that regulation of COPII turnover can explain the influence of Sec16 on tER sites. During the budding of coat protein complex II (COPII) vesicles from transitional endoplasmic reticulum (tER) sites, Sec16 has been proposed to play two distinct roles: negatively regulating COPII turnover and organizing COPII assembly at tER sites. We tested these ideas using the yeast Pichia pastoris. Redistribution of Sec16 to the cytosol accelerates tER dynamics, supporting a negative regulatory role for Sec16. To evaluate a possible COPII organization role, we dissected the functional regions of Sec16. The central conserved domain, which had been implicated in coordinating COPII assembly, is actually dispensable for normal tER structure. An upstream conserved region (UCR) localizes Sec16 to tER sites. The UCR binds COPII components, and removal of COPII from tER sites also removes Sec16, indicating that COPII recruits Sec16 rather than the other way around. We propose that Sec16 does not in fact organize COPII. Instead, regulation of COPII turnover can account for the influence of Sec16 on tER sites.