Department of Physiology and Biophysics, University of Arkansas for Medical Sciences, Little Rock, AR, 72205, USA.
Sci Rep. 2020 Oct 6;10(1):16604. doi: 10.1038/s41598-020-73276-w.
Rab6, the most abundant Golgi associated small GTPase, consists of 2 equally common isoforms, Rab6A and Rab6A', that differ in 3 amino acids and localize to trans Golgi cisternae. The two isoforms are largely redundant in function and hence are often referred to generically as Rab6. Rab6 loss-of-function inhibits retrograde Golgi trafficking, induces an increase in Golgi cisternal number in HeLa cells and delays the cell surface appearance of the anterograde cargo protein, VSVG. We hypothesized that these effects are linked and might be explained by a cisternal-specific delay in cargo transport. In pulse chase experiments using a deconvolved, confocal line scanning approach to score the distribution of the tsO45 mutant of VSVG protein in Rab6 depleted cells, we found that anterograde transport at 32 °C, permissive conditions, through the Golgi apparatus was locally delayed, almost tenfold, between medial and trans Golgi cisterna. Cis to medial transport was nearly normal as was trans Golgi to TGN transport. TGN exit was unaffected by Rab6 depletion. These effects were the same with either of two siRNAs. Similar intra-Golgi transport delays were seen at 37 °C with RUSH VSVG or a RUSH GPI-anchored construct using a biotin pulse to release the marker proteins from the ER. Using 3D-SIM, a super resolution approach, we found that RUSH VSVG transport was delayed pre-trans Golgi. These visual approaches suggest a selective slowing of anterograde transport relative to 3 different marker proteins downstream of the trans Golgi. Using a biochemical approach, we found that the onset of VSVG endoglycosidase H resistance in Rab6 depleted cells was delayed. Depletion of neither Rab6A or Rab6A' isoforms alone had any effect on anterograde transport through the Golgi suggesting that Rab6A and Rab6A' act coordinately. Delayed cargo transport conditions correlate strongly with a proliferation of Golgi cisternae observed in earlier electron microscopy. Our results strongly indicate that Rab6 is selectively required for rapid anterograde transport from the medial to trans Golgi. We suggest that the observed correlation with localized cisternal proliferation fits best with a cisternal progression model of Golgi function.
Rab6 是高尔基体相关的小 GTP 酶中最丰富的一种,由两种同样常见的同工型组成,Rab6A 和 Rab6A',它们在 3 个氨基酸上有所不同,定位于反式高尔基体潴腔。这两种同工型在功能上基本是冗余的,因此通常被笼统地称为 Rab6。Rab6 功能丧失会抑制逆行高尔基体运输,在 HeLa 细胞中诱导高尔基体潴腔数量增加,并延迟顺向货物蛋白 VSVG 的细胞表面出现。我们假设这些效应是相关的,可能可以用货物运输在潴腔中的特定延迟来解释。在使用去卷积共聚焦线扫描方法来评分 Rab6 耗竭细胞中 tsO45 突变型 VSVG 蛋白分布的脉冲追踪实验中,我们发现,在 32°C(允许条件下),顺行运输通过高尔基体时,在中间和反式高尔基体潴腔之间几乎延迟了十倍。顺向到中间的运输几乎正常,反式高尔基体到 TGN 的运输也是如此。TGN 出口不受 Rab6 耗竭的影响。这两种效应在两种 siRNA 中都是相同的。用 RUSH VSVG 或生物素脉冲释放 ER 中的标记蛋白的 Rush GPI 锚定构建体在 37°C 时也观察到类似的高尔基体内部运输延迟。使用 3D-SIM(超分辨率方法),我们发现 RUSH VSVG 运输在顺式高尔基体之前就被延迟了。这些直观的方法表明,相对于反式高尔基体下游的 3 种不同的标记蛋白,顺行运输被选择性地减缓。使用生化方法,我们发现 Rab6 耗竭细胞中 VSVG 内切糖苷酶 H 抗性的起始延迟。单独耗尽 Rab6A 或 Rab6A'同工型对高尔基体中的顺行运输没有任何影响,这表明 Rab6A 和 Rab6A' 协同作用。延迟的货物运输条件与早期电子显微镜观察到的高尔基体潴腔增殖强烈相关。我们的结果强烈表明,Rab6 是从中间到反式高尔基体快速顺行运输所必需的。我们认为,与局部潴腔增殖的观察结果最吻合的是高尔基体功能的潴腔进展模型。