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Reconstitution of autophagosome nucleation defines Atg9 vesicles as seeds for membrane formation

机译:自噬核心成核的重建将ATG9囊泡定义为膜形成的种子

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摘要

Autophagosomes form de novo in a manner that is incompletely understood. Particularly enigmatic are autophagy-related protein 9 (Atg9)-containing vesicles that are required for autophagy machinery assembly but do not supply the bulk of the autophagosomal membrane. In this study, we reconstituted autophagosome nucleation using recombinant components from yeast. We found that Atg9 proteoliposomes first recruited the phosphatidylinositol 3-phosphate kinase complex, followed by Atg21, the Atg2-Atg18 lipid transfer complex, and the E3-like Atg12-Atg5-Atg16 complex, which promoted Atg8 lipidation. Furthermore, we found that Atg2 could transfer lipids for Atg8 lipidation. In selective autophagy, these reactions could potentially be coupled to the cargo via the Atg19-Atg11-Atg9 interactions. We thus propose that Atg9 vesicles form seeds that establish membrane contact sites to initiate lipid transfer from compartments such as the endoplasmic reticulum.
机译:自噬体以不完全理解的方式形成de novo。特别神奇的是与自噬相关的蛋白质9(ATG9) - 甲型自噬机械组件所需的囊泡,但不提供大量的自噬复印膜。在该研究中,我们使用来自酵母的重组组分重构自噬体成核。我们发现ATG9蛋白质体首先募集磷脂酰肌醇3-磷酸激酶络合物,其次是ATG21,ATG2-ATG18脂质转移络合物,以及E3样ATG12-ATG5-ATG16复合物,其促进了ATG8脂质。此外,我们发现ATG2可以转移脂质的ATG8脂质。在选择性自噬中,这些反应可能通过ATG19-ATG11-ATG9相互作用耦合到货物。因此,我们提出了ATG9囊泡形成种子,该种子建立膜接触位点,以从诸如内质网的隔室开始脂质转移。

著录项

  • 来源
    《Science》 |2020年第6508期|1206-1206|共1页
  • 作者单位

    Univ Vienna Max Perutz Labs Dept Biochem & Cell Moira A-1030 Vienna Austria;

    Univ Vienna Max Perutz Labs Dept Biochem & Cell Moira A-1030 Vienna Austria;

    Univ Vienna Max Perutz Labs Dept Biochem & Cell Moira A-1030 Vienna Austria;

    Max Planck Inst Biophys Dept Theoret Biophys D-60438 Frankfurt Germany;

    Univ Vienna Max Perutz Labs Dept Biochem & Cell Moira A-1030 Vienna Austria;

    Univ Vienna Max Perutz Labs Dept Biochem & Cell Moira A-1030 Vienna Austria;

    Univ Vienna Max Perutz Labs Dept Biochem & Cell Moira A-1030 Vienna Austria;

    Max Planck Inst Biol Ageing D-50931 Cologne Germany|Univ Cologne Cologne Excellence Cluster Cellular Stress Respon D-50931 Cologne Germany;

    Max Planck Inst Biophys Dept Theoret Biophys D-60438 Frankfurt Germany|Goethe Univ Frankfurt Inst Biophys D-60438 Frankfurt Germany;

    Univ Vienna Max Perutz Labs Dept Biochem & Cell Moira A-1030 Vienna Austria;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-18 22:15:13

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