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Rab GTPases: master regulators that establish the secretory and endocytic pathways

机译:Rab GTPases:建立分泌和内吞途径的主要调节剂

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摘要

Several of the most important discoveries in the field of membrane traffic have come from studies of Rab GTPases by Marino Zerial and Peter Novick and their colleagues. Zerial was the first to discover that Rab GTPases represent identity markers for different membrane-bound compartments, and each Rab organizes a collection of specific effectors into function-specifying membrane microdomains to carry out receptor trafficking. Novick discovered that the order (and thus polarity) of Rab GTPases along the secretory and endocytic pathways are established by their specific, cognate guanine nucleotide exchange factors (GEFs) and GTPase-activating proteins (GAPs), which partner with one Rab to regulate the subsequent- and prior-acting Rabs. Such so-called Rab cascades have evolved to establish domains that contain unique Rab proteins and their cognate effectors, which drive all steps of membrane trafficking. These findings deserve much broader recognition by the biomedical research community and are highlighted here, along with open questions that require serious attention for full understanding of the molecular basis of Rab GTPase-regulated membrane trafficking in eukaryotic cells.
机译:膜运输领域中最重要的发现来自Marino Zerial和Peter Novick及其同事对Rab GTPases的研究。 Zerial是第一个发现Rab GTPases代表不同膜结合区室的身份标记的人,每个Rab都将一组特定的效应子组织到功能指定的膜微区中,以进行受体运输。 Novick发现,Rab GTPases沿分泌和内吞途径的顺序(以及极性)是由它们的特异性同源鸟嘌呤核苷酸交换因子(GEF)和GTPase激活蛋白(GAP)共同建立的,它们与一个Rab共同调节后续行动和先前行动的Rab。这种所谓的Rab级联已经进化为建立包含独特Rab蛋白及其同源效应子的域,这些域驱动着膜运输的所有步骤。这些发现应得到生物医学研究界的广泛认可,并在此处强调,还有一些开放的问题需要认真关注,以充分了解Rab GTPase调控的真核细胞膜运输的分子基础。

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