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The vacuolar transporter chaperone (VTC) complex is required for microautophagy

机译:微自噬需要液泡转运蛋白伴侣(VTC)复合物

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摘要

Microautophagy involves direct invagination and fission of the vacuolar/lysosomal membrane under nutrient limitation. This occurs by an autophagic tube, a specialized vacuolar membrane invagination that pinches off vesicles into the vacuolar lumen. In this study we have identified the VTC (vacuolar transporter chaperone) complex as required for microautophagy. The VTC complex is present on the ER and vacuoles and at the cell periphery. On induction of autophagy by nutrient limitation the VTC complex is recruited to and concentrated on vacuoles. The VTC complex is inhomogeneously distributed within the vacuolar membranes, showing an enrichment on autophagic tubes. Deletion of the VTC complex blocks microautophagic uptake into vacuoles. The mutants still form autophagic tubes but the production of microautophagic vesicles from their tips is impaired. In line with this, affinity-purified antibodies to the Vtc proteins inhibit microautophagic uptake in a reconstituted system in vitro. Our data suggest that the VTC complex is an important constituent of autophagic tubes and that it is required for scission of microautophagic vesicles from these tubes.
机译:微自噬涉及在营养限制下液泡/溶酶体膜的直接内陷和裂变。这是通过自噬管发生的,自噬管是一种特殊的液泡膜内陷,可将囊泡压入液泡腔。在这项研究中,我们确定了微自噬所需的VTC(真空转运蛋白伴侣)复合物。 VTC复合物存在于ER和液泡以及细胞外围。通过营养限制诱导自噬后,VTC复合物被募集到液泡中并浓缩。 VTC复合物不均匀地分布在液泡膜内,显示在自噬管上富集。 VTC复合物的删除会阻止微自噬进入液泡。突变体仍然形成自噬管,但是从其尖端产生的微自噬囊泡受到损害。与此相符,针对Vtc蛋白的亲和纯化抗体可在体外重构系统中抑制微自噬摄取。我们的数据表明,VTC复合物是自噬管的重要组成部分,是从这些管切开微自噬囊泡所必需的。

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