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秀丽隐杆线虫的Tubby蛋白通过两种独立机制调节寿命和脂肪储存。

C. elegans tubby regulates life span and fat storage by two independent mechanisms.

作者信息

Mukhopadhyay Arnab, Deplancke Bart, Walhout Albertha J M, Tissenbaum Heidi A

出版信息

Cell Metab. 2005 Jul;2(1):35-42. doi: 10.1016/j.cmet.2005.06.004.

Abstract

In C. elegans, similar to in mammals, mutations in the tubby homolog, tub-1, promote increased fat deposition. Here, we show that mutation in tub-1 also leads to life span extension dependent on daf-16/FOXO. Interestingly, function of tub-1 in fat storage is independent of daf-16. A yeast two-hybrid screen identified a novel TUB-1 interaction partner (RBG-3); a RabGTPase-activating protein. Both TUB-1 and RBG-3 localize to overlapping neurons. Importantly, RNAi of rbg-3 decreases fat deposition in tub-1 mutants but does not affect life span. We demonstrate that TUB-1 is expressed in ciliated neurons and undergoes both dendritic and ciliary transport. Additionally, tub-1 mutants are chemotaxis defective. Thus, tub-1 may regulate fat storage either by modulating transport, sensing, or responding to signals in ciliated neurons. Taken together, we define a role for tub-1 in regulation of life span and show that tub-1 regulates life span and fat storage by two independent mechanisms.

摘要

在秀丽隐杆线虫中,与哺乳动物类似,类Tubby蛋白同源物tub-1发生突变会促进脂肪沉积增加。在此,我们表明tub-1突变也会导致依赖daf-16/FOXO的寿命延长。有趣的是,tub-1在脂肪储存中的功能独立于daf-16。酵母双杂交筛选鉴定出一种新型的TUB-1相互作用蛋白(RBG-3);一种Rab鸟苷酸三磷酸酶激活蛋白。TUB-1和RBG-3都定位于重叠的神经元。重要的是,对rbg-3进行RNA干扰会减少tub-1突变体中的脂肪沉积,但不影响寿命。我们证明TUB-1在纤毛神经元中表达,并经历树突和纤毛运输。此外,tub-1突变体存在趋化缺陷。因此,tub-1可能通过调节纤毛神经元中的运输、感知或对信号的反应来调节脂肪储存。综上所述,我们确定了tub-1在寿命调节中的作用,并表明tub-1通过两种独立机制调节寿命和脂肪储存。

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