From the Departments of Biochemistry and.
Chemistry and Biomolecular Chemistry, University of Wisconsin, Madison, Wisconsin 53706.
J Biol Chem. 2014 Sep 5;289(36):25276-86. doi: 10.1074/jbc.M114.575985. Epub 2014 Jul 7.
The abundance and functional activity of proteins involved in the formation of the SNARE complex are tightly regulated for efficient exocytosis. Tomosyn proteins are negative regulators of exocytosis. Tomosyn causes an attenuation of insulin secretion by limiting the formation of the SNARE complex. We hypothesized that glucose-dependent stimulation of insulin secretion from β-cells must involve reversing the inhibitory action of tomosyn. Here, we show that glucose increases tomosyn protein turnover. Within 1 h of exposure to 15 mM glucose, ~50% of tomosyn was degraded. The degradation of tomosyn in response to high glucose was blocked by inhibitors of the proteasomal pathway. Using (32)P labeling and mass spectrometry, we showed that tomosyn-2 is phosphorylated in response to high glucose, phorbol esters, and analogs of cAMP, all key insulin secretagogues. We identified 11 phosphorylation sites in tomosyn-2. Site-directed mutagenesis was used to generate phosphomimetic (Ser → Asp) and loss-of-function (Ser → Ala) mutants. The Ser → Asp mutant had enhanced protein turnover compared with the Ser → Ala mutant and wild type tomosyn-2. Additionally, the Ser → Asp tomosyn-2 mutant was ineffective at inhibiting insulin secretion. Using a proteomic screen for tomosyn-2-binding proteins, we identified Hrd-1, an E3-ubiquitin ligase. We showed that tomosyn-2 ubiquitination is increased by Hrd-1, and knockdown of Hrd-1 by short hairpin RNA resulted in increased abundance in tomosyn-2 protein levels. Taken together, our results reveal a mechanism by which enhanced phosphorylation of a negative regulator of secretion, tomosyn-2, in response to insulin secretagogues targets it to degradation by the Hrd-1 E3-ubiquitin ligase.
参与 SNARE 复合物形成的蛋白质的丰度和功能活性受到严格调控,以实现有效的胞吐作用。Tomosyn 蛋白是胞吐作用的负调节剂。Tomosyn 通过限制 SNARE 复合物的形成来减弱胰岛素的分泌。我们假设β细胞中葡萄糖依赖性的胰岛素分泌刺激必须涉及逆转 Tomosyn 的抑制作用。在这里,我们表明葡萄糖增加了 Tomosyn 蛋白的周转率。在暴露于 15mM 葡萄糖 1 小时内,约 50%的 Tomosyn 被降解。高葡萄糖对 Tomosyn 降解的抑制作用被蛋白酶体途径抑制剂阻断。使用(32)P 标记和质谱分析,我们表明 Tomosyn-2 在高葡萄糖、佛波酯和 cAMP 类似物的刺激下发生磷酸化,这些都是关键的胰岛素分泌激动剂。我们在 Tomosyn-2 中鉴定了 11 个磷酸化位点。通过定点突变生成了磷酸模拟(Ser→Asp)和功能丧失(Ser→Ala)突变体。与 Ser→Ala 突变体和野生型 Tomosyn-2 相比,Ser→Asp 突变体的蛋白周转率更高。此外,Ser→Asp Tomosyn-2 突变体在抑制胰岛素分泌方面无效。通过 Tomosyn-2 结合蛋白的蛋白质组学筛选,我们鉴定了 Hrd-1,一种 E3 泛素连接酶。我们表明 Tomosyn-2 的泛素化通过 Hrd-1 增加,并且通过短发夹 RNA 敲低 Hrd-1 导致 Tomosyn-2 蛋白水平增加。总之,我们的结果揭示了一种机制,即响应胰岛素分泌激动剂,负调节分泌的 Tomosyn-2 的磷酸化增强将其靶向 Hrd-1 E3 泛素连接酶进行降解。