首页> 美国卫生研究院文献>Journal of Experimental Botany >Stacks off tracks: a role for the golgin AtCASP in plant endoplasmic reticulum-Golgi apparatus tethering
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Stacks off tracks: a role for the golgin AtCASP in plant endoplasmic reticulum-Golgi apparatus tethering

机译:偏离轨道:高尔金AtCASP在植物内质网-高尔基体系留系中的作用

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摘要

The plant Golgi apparatus modifies and sorts incoming proteins from the endoplasmic reticulum (ER) and synthesizes cell wall matrix material. Plant cells possess numerous motile Golgi bodies, which are connected to the ER by yet to be identified tethering factors. Previous studies indicated a role for cis-Golgi plant golgins, which are long coiled-coil domain proteins anchored to Golgi membranes, in Golgi biogenesis. Here we show a tethering role for the golgin AtCASP at the ER-Golgi interface. Using live-cell imaging, Golgi body dynamics were compared in Arabidopsis thaliana leaf epidermal cells expressing fluorescently tagged AtCASP, a truncated AtCASP-ΔCC lacking the coiled-coil domains, and the Golgi marker STtmd. Golgi body speed and displacement were significantly reduced in AtCASP-ΔCC lines. Using a dual-colour optical trapping system and a TIRF-tweezer system, individual Golgi bodies were captured in planta. Golgi bodies in AtCASP-ΔCC lines were easier to trap and the ER-Golgi connection was more easily disrupted. Occasionally, the ER tubule followed a trapped Golgi body with a gap, indicating the presence of other tethering factors. Our work confirms that the intimate ER-Golgi association can be disrupted or weakened by expression of truncated AtCASP-ΔCC and suggests that this connection is most likely maintained by a golgin-mediated tethering complex.
机译:植物高尔基体装置修饰并分选来自内质网(ER)的进入蛋白质,并合成细胞壁基质材料。植物细胞拥有众多能动的高尔基体,它们通过尚未确定的束缚因子与内质网相连。先前的研究表明,在高尔基体生物发生中,顺式-高尔基体植物蛋白是一种锚定在高尔基体膜上的长螺旋线圈结构域蛋白。在这里,我们在ER-Golgi界面上显示了golgin AtCASP的绑定功能。使用活细胞成像,比较了表达荧光标记的AtCASP,缺少卷曲螺旋结构域的截短的AtCASP-ΔCC和高尔基标记STtmd的拟南芥叶表皮细胞中的高尔基体动力学。在AtCASP-ΔCC品系中,高尔基体速度和位移显着降低。使用双色光学捕获系统和TIRF镊子系统,在植物中捕获了单个高尔基体。 AtCASP-ΔCC系中的高尔基体更容易被捕获,ER-高尔基体的连接更容易被破坏。有时,ER小管跟随高尔基体被捕获,并留有缝隙,表明存在其他栓系因子。我们的工作证实,截短的AtCASP-ΔCC的表达可以破坏或削弱紧密的ER-高尔基体,并暗示这种连接最有可能由古尔金介导的束缚复合体维持。

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