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Mapping the Interactome of the Nuclear Heparan Sulfate Proteoglycan Syndecan-1 in Mesothelioma Cells

机译:在间皮瘤细胞中映射核普普林硫酸乙酸硫酸甘油蛋白蛋白增生蛋白二烷二烷二烷二烷二烷二烷二烷基

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摘要

Syndecan-1 (SDC1) is a cell surface heparan sulfate proteoglycan (HSPG), which regulates various signaling pathways controlling the proliferation and migration of malignant mesothelioma and other types of cancer. We have previously shown that SDC1 can translocate to the nucleus in mesothelioma cells through a tubulin-dependent transport mechanism. However, the role of nuclear SDC1 is largely unknown. Here, we performed co-immunoprecipitation (Co-IP) of SDC1 in a mesothelioma cell line to identify SDC1 interacting proteins. The precipitates contained a large number of proteins, indicating the recovery of protein networks. Proteomic analysis with a focus on nuclear proteins revealed an association with pathways related to cell proliferation and RNA synthesis, splicing and transport. In support of this, the top RNA splicing candidates were verified to interact with SDC1 by Co-IP and subsequent Western blot analysis. Further loss- and gain-of-function experiments showed that SDC1 influences RNA levels in mesothelioma cells. The results identify a proteomic map of SDC1 nuclear interactors in a mesothelioma cell line and suggest a previously unknown role for SDC1 in RNA biogenesis. The results should serve as a fundament for further studies to discover the role of nuclear SDC1 in normal and cancer cells of different origin.
机译:Syndecan-1(SDC1)是一种细胞表面硫酸普普林蛋白蛋白多糖(HSPG),其调节控制恶性间皮瘤和其他类型的癌症的增殖和迁移的各种信号通路。我们之前已经表明,SDC1可以通过依赖于管蛋白依赖性的运输机制将SDC1易于中核核心。但是,核SDC1的作用在很大程度上是未知的。这里,我们在间皮瘤细胞系中进行了SDC1的共免疫沉淀(CO-IP)以鉴定SDC1相互作用蛋白。沉淀物含有大量蛋白质,表明蛋白质网络的回收率。具有关注核蛋白质的蛋白质组学分析显示与与细胞增殖和RNA合成,剪接和运输有关的途径相关性。为了支持这一点,通过CO-IP和随后的Western印迹分析验证了顶部RNA剪接候选者以与SDC1相互作用。进一步的丧失和功能性实验表明,SDC1影响间皮瘤细胞中的RNA水平。结果鉴定了间皮瘤细胞系中SDC1核交互式的蛋白质组学图,并表明了RNA生物发生中SDC1的先前未知的作用。结果应作为进一步研究的基础,以发现核SDC1在不同起源的正常和癌细胞中的作用。

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