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Live cell imaging of the assembly disassembly and actin cable–dependent movement of endosomes and actin patches in the budding yeast Saccharomyces cerevisiae

机译:酵母酿酒酵母中内体和肌动蛋白斑块的组装拆卸和肌动蛋白电缆依赖性运动的活细胞成像

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摘要

Using FM4-64 to label endosomes and Abp1p-GFP or Sac6p-GFP to label actin patches, we find that (1) endosomes colocalize with actin patches as they assemble at the bud cortex; (2) endosomes colocalize with actin patches as they undergo linear, retrograde movement from buds toward mother cells; and (3) actin patches interact with and disassemble at FM4-64–labeled internal compartments. We also show that retrograde flow of actin cables mediates retrograde actin patch movement. An Arp2/3 complex mutation decreases the frequency of cortical, nonlinear actin patch movements, but has no effect on the velocity of linear, retrograde actin patch movement. Rather, linear actin patch movement occurs at the same velocity and direction as the movement of actin cables. Moreover, actin patches require actin cables for retrograde movements and colocalize with actin cables as they undergo retrograde movement. Our studies support a mechanism whereby actin cables serve as “conveyor belts” for retrograde movement and delivery of actin patches/endosomes to FM4-64–labeled internal compartments.
机译:使用FM4-64标记内体,用Abp1p-GFP或Sac6p-GFP标记肌动蛋白斑,我们发现(1)内体在肌芽膜组装时与肌动蛋白斑共定位; (2)内体与肌动蛋白斑共定位,因为它们经历从芽到母细胞的线性逆行运动; (3)肌动蛋白补丁在FM4-64标记的内部区室中相互作用并分解。我们还显示肌动蛋白电缆的逆行流动介导了肌动蛋白补丁的逆行运动。 Arp2 / 3复合突变降低了皮质的非线性肌动蛋白补丁运动的频率,但对线性逆行的肌动蛋白补丁运动的速度没有影响。而是,线性肌动蛋白膜片运动以与肌动蛋白电缆的运动相同的速度和方向发生。此外,肌动蛋白补丁需要肌动蛋白电缆进行逆行运动,并在肌动蛋白电缆进行逆行运动时与肌动蛋白电缆共定位。我们的研究支持一种机制,肌动蛋白电缆充当“传送带”,用于逆行运动以及将肌动蛋白贴片/内体传递到FM4-64标记的内部隔室。

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