Lőrincz Péter, Tóth Sarolta, Benkő Péter, Lakatos Zsolt, Boda Attila, Glatz Gábor, Zobel Martina, Bisi Sara, Hegedűs Krisztina, Takáts Szabolcs, Scita Giorgio, Juhász Gábor
Department of Anatomy, Cell and Developmental Biology, Eötvös Loránd University, Budapest H-1117, Hungary.
Institute of Genetics, Biological Research Centre, Hungarian Academy of Sciences, Szeged H-6726, Hungary.
J Cell Biol. 2017 Jul 3;216(7):1937-1947. doi: 10.1083/jcb.201611027. Epub 2017 May 8.
Rab7 promotes fusion of autophagosomes and late endosomes with lysosomes in yeast and metazoan cells, acting together with its effector, the tethering complex HOPS. Here we show that another small GTPase, Rab2, is also required for autophagosome and endosome maturation and proper lysosome function in We demonstrate that Rab2 binds to HOPS, and that its active, GTP-locked form associates with autolysosomes. Importantly, expression of active Rab2 promotes autolysosomal fusions unlike that of GTP-locked Rab7, suggesting that its amount is normally rate limiting. We also demonstrate that RAB2A is required for autophagosome clearance in human breast cancer cells. In conclusion, we identify Rab2 as a key factor for autophagic and endocytic cargo delivery to and degradation in lysosomes.
Rab7在酵母和后生动物细胞中促进自噬体和晚期内体与溶酶体的融合,与其效应器拴系复合物HOPS共同发挥作用。在此,我们表明另一种小GTP酶Rab2对于自噬体和内体的成熟以及溶酶体在中的正常功能也是必需的。我们证明Rab2与HOPS结合,并且其活性的、GTP锁定形式与自噬溶酶体相关联。重要的是,与GTP锁定的Rab7不同,活性Rab2的表达促进自噬溶酶体融合,这表明其数量通常是限速因素。我们还证明RAB2A对于人乳腺癌细胞中自噬体的清除是必需的。总之,我们确定Rab2是自噬和内吞货物运输到溶酶体并在溶酶体中降解的关键因素。