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作为调节脂肪储存的塔比蛋白作用靶点的内吞途径。

An endocytic pathway as a target of tubby for regulation of fat storage.

作者信息

Mukhopadhyay Arnab, Pan Xiaojing, Lambright David G, Tissenbaum Heidi A

机构信息

Program in Gene Function and Expression, University of Massachusetts Medical School, 364 Plantation Street, Worcester, Massachusetts 01605, USA.

出版信息

EMBO Rep. 2007 Oct;8(10):931-8. doi: 10.1038/sj.embor.7401055. Epub 2007 Aug 31.

Abstract

The tubby loci provide a unique opportunity to study adult-onset obesity. Mutation in either mammalian tubby or its homologue in Caenorhabditis elegans, tub-1, results in increased fat storage. Previously, we have shown that TUB-1 interacts with a new Rab GTPase-activating protein, RBG-3, for the regulation of fat storage. To understand further the molecular mechanism of TUB-1, we identified the Rab GTPase downstream of RBG-3. We found that RBG-3 preferentially stimulates the intrinsic GTPase activity of RAB-7 in both human and C. elegans. Importantly, either mutation or RNA interference knockdown in rab-7 reduces stored fat in wild type and tub-1 mutants. In addition, the small GTPase rab-5 and genes that regulate Rab membrane localization and nucleotide recycling are required for the regulation of fat storage, thereby defining a role for endocytic recycling in this process. We propose that TUB-1 controls receptor or sensory molecule degradation in neurons by regulating a RAB-7-mediated endocytic pathway.

摘要

肥胖基因座为研究成人期肥胖提供了一个独特的机会。哺乳动物的Tubby基因或其在秀丽隐杆线虫中的同源物tub-1发生突变,都会导致脂肪储存增加。此前,我们已经表明TUB-1与一种新的Rab GTP酶激活蛋白RBG-3相互作用,以调节脂肪储存。为了进一步了解TUB-1的分子机制,我们确定了RBG-3下游的Rab GTP酶。我们发现,RBG-3在人和秀丽隐杆线虫中都优先刺激RAB-7的内在GTP酶活性。重要的是,rab-7中的突变或RNA干扰敲低会减少野生型和tub-1突变体中的储存脂肪。此外,小GTP酶rab-5以及调节Rab膜定位和核苷酸循环的基因对于脂肪储存的调节是必需的,从而确定了内吞循环在这个过程中的作用。我们提出,TUB-1通过调节RAB-7介导的内吞途径来控制神经元中受体或感觉分子的降解。

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