Maturation of late Golgi cisternae into RabE(RAB11) exocytic post-Golgi carriers visualized in vivo.
Maturation of late Golgi cisternae into RabE(RAB11) exocytic post-Golgi carriers visualized in vivo.
复制标题
晚期高尔基体池成熟为 RabE(RAB11) 胞吐后高尔基体载体,在体内可视化。
DOI:
10.1091/mbc.e14-02-0710
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发表时间:
2014-08-15
影响因子:
3.3
通讯作者:
Peñalva MA
中科院分区:
文献类型:
--
作者:
Pantazopoulou A;Pinar M;Xiang X;Peñalva MA
Maturation of Golgi cisternae into post-Golgi carriers is directly visualized using the Aspergillus nidulans Ypt31/RAB11 homologue RabE as a reporter of post-Golgi identity. A microtubule-based conveyor belt fuels carriers to actin microfilaments radiating from the apex, which carry out the membrane-proximal transport step of exocytosis. The mechanism(s) by which proteins traverse and exit the Golgi are incompletely understood. Using Aspergillus nidulans hyphae, we show that late Golgi cisternae undergo changes in composition to gradually lose Golgi identity while acquiring post-Golgi RabERAB11 identity. This behavior of late Golgi cisternae is consistent with the cisternal maturation model. Post-Golgi RabERAB11 carriers travel to, and accumulate at, the apex, indicating that fusion is rate limiting for exocytosis. These carriers, which are loaded with kinesin, dynein, and MyoEMYO5, move on a microtubule-based bidirectional conveyor belt relaying them to actin, which ultimately focuses exocytosis at the apex. Dynein drags RabERAB11 carriers away if engagement of MyoEMYO5 to actin cables fails. Microtubules seemingly cooperating with F-actin capture can sustain secretion if MyoEMYO5 is absent. Thus, filamentous fungal secretion involving post-Golgi carriers is remarkably similar, mechanistically, to the transport of melanosomes in melanocyte dendrites, even though melanosome biogenesis involves lysosomes rather than Golgi.