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首页> 外文期刊>Journal of cell biology >Peroxisomes move by hitchhiking on early endosomes using the novel linker protein PxdA
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Peroxisomes move by hitchhiking on early endosomes using the novel linker protein PxdA

机译:过氧化物酶体通过使用新型接头蛋白PxdA在早期的内体上搭便车而移动

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摘要

Eukaryotic cells use microtubule-based intracellular transport for the delivery of many subcellular cargos, including organelles. The canonical view of organelle transport is that organelles directly recruit molecular motors via cargo-specific adaptors. In contrast with this view, we show here that peroxisomes move by hitchhiking on early endosomes, an organelle that directly recruits the transport machinery. Using the filamentous fungus Aspergillus nidulans we found that hitchhiking is mediated by a novel endosome-associated linker protein, PxdA. PxdA is required for normal distribution and long-range movement of peroxisomes, but not early endosomes or nuclei. Using simultaneous time-lapse imaging, we find that early endosome-associated PxdA localizes to the leading edge of moving peroxisomes. We identify a coiled-coil region within PxdA that is necessary and sufficient for early endosome localization and peroxisome distribution and motility. These results present a new mechanism of microtubule-based organelle transport in which peroxisomes hitchhike on early endosomes and identify PxdA as the novel linker protein required for this coupling.
机译:真核细胞使用基于微管的细胞内运输来递送许多亚细胞货物,包括细胞器。规范的细胞器运输观点是,细胞器通过货物专用的衔接子直接募集分子马达。与这种观点相反,我们在这里显示过氧化物酶体通过搭便车在早期的内体上移动,内体是一种直接募集运输机械的细胞器。使用丝状真菌构巢曲霉,我们发现搭便车是由新型的内体相关接头蛋白PxdA介导的。 PxdA是过氧化物酶体的正常分布和远距离运动所必需的,而早期的内体或细胞核则不需要。使用同步延时成像,我们发现早期的内体相关的PxdA定位到移动过氧化物酶体的前沿。我们在PxdA内识别出一个盘绕线圈区域,该区域对于早期内体定位,过氧化物酶体分布和运动性是必要和充分的。这些结果提出了一种基于微管的细胞器运输的新机制,其中过氧化物酶体在早期的内体上搭便车,并将PxdA鉴定为这种偶联所需的新型接头蛋白。

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