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ER Contact Sites Define the Position and Timing of Endosome Fission

机译:ER接触部位确定了内体裂变的位置和时机

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摘要

Endocytic cargo and Rab GTPases are segregated to distinct domains of an endosome. These domains maintain their identity until they undergo fission to traffic cargo. It is not fully understood how segregation of cargo or Rab proteins is maintained along the continuous endosomal membrane or what machinery is required for fission. Endosomes form contact sites with the endoplasmic reticulum (ER) that are maintained during trafficking. Here, we show that stable contacts form between the ER and endosome at constricted sorting domains, and free diffusion of cargo is limited at these positions. We demonstrate that the site of constriction and fission for early and late endosomes is spatially and temporally linked to contact sites with the ER. Lastly, we show that altering ER structure and dynamics reduces the efficiency of endosome fission. Together, these data reveal a surprising role for ER contact in defining the timing and position of endosome fission.
机译:内吞货物和Rab GTPases被分离到内体的不同区域。这些域保持其身份,直到它们发生裂变以运输货物为止。尚未完全理解如何沿连续的内体膜维持货物或Rab蛋白的分离,或裂变需要何种机制。内体与运输过程中维持的内质网(ER)形成接触位点。在这里,我们显示了在狭窄的分选域内,内质网和内体之间形成了稳定的接触,货物的自由扩散在这些位置受到限制。我们证明早期和晚期内体的收缩和裂变位点在空间和时间上都与内质网的接触位点相关。最后,我们表明,改变内质网的结构和动力学会降低内体裂变的效率。总之,这些数据揭示了ER接触在定义内体裂变的时间和位置方面的令人惊讶的作用。

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