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

机译:Rab GTP酶:建立分泌和内吞径的母部调节剂

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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:膜交通领域的几个最重要的发现来自Marino Zerial和Peter Novick及其同事的Rab GTP酶的研究。 Zerial是第一个发现Rab GTP酶代表不同膜结合隔室的身份标记,并且每个RAB组织一种特定效应器的集合成功能指定的膜微瘤以进行受体贩运。 Novick发现,沿着分泌物和内吞枢纽的Rab GTP酶的顺序(以及因此极性)由其特异性,同源的鸟嘌呤核苷酸交换因子(GEF)和GTP酶活性蛋白质(间隙)建立,其与一个RAB合作以调节后续和先前的rabs。这种所谓的RAB级联已经发展以建立含有独特的Rab蛋白及其同源效应的结构域,其驱动所有膜运输的所有步骤。这些调查结果值得生物医学研究界的更广泛的认可,并在这里突出显示,以及需要认真注意的开放性问题,以便完全了解RAB GTP酶监管膜流量在真核细胞中的分子基础。

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