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The interactome and proteomic responses of ALKBH7 in cell lines by in-depth proteomics analysis

机译:深入蛋白质组学分析,Cell系中AlkBH7的互动组和蛋白质组学反应

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Background:ALKBH7 is a mitochondrial protein, involved in programmed necrosis, fatty acid metabolism, cell cycle regulation, and prostate cancer disease. However, the exact roles of ALKBH7 and the underlying molecular mechanisms remain mysterious. Thus, investigations of the interactome and proteomic responses of ALKBH7 in cell lines using proteomics strategies are urgently required.Methods:In the present study, we investigated the interactome of ALKBH7 in mitochondria through immunoprecipitation-mass spectrometry/mass spectrometry (IP-MS/MS). Additionally, we established the ALKBH7 knockdown and overexpression cell lines and further identified the differentially expressed proteins (DEPs) in these cell lines by TMT-based MS/MS. Two DEPs (UQCRH and HMGN1) were validated by western blotting analysis.Results:Through bioinformatic analysis the proteomics data, we found that ALKBH7 was involved in protein homeostasis and cellular immunity, as well as cell proliferation, lipid metabolism, and programmed necrosis by regulating the expression of PTMA, PTMS, UQCRH, HMGN1, and HMGN2. Knockdown of ALKBH7 resulted in upregulation of UQCRH and HMGN1 expression, and the opposite pattern of expression was detected in ALKBH7 overexpression cell lines; these results were consistent with our proteomics data.Conclusion:Our findings indicate that the expression of UQCRH and HMGN1 is regulated by ALKBH7, which provides potential directions for future studies of ALKBH7. Furthermore, our results also provide comprehensive insights into the molecular mechanisms and pathways associated with ALKBH7.? The Author(s). 2019.
机译:背景:ALKBH7是线粒体蛋白质,参与编程坏死,脂肪酸代谢,细胞周期调节和前列腺癌疾病。然而,ALKBH7和潜在的分子机制的确切作用仍然是神秘的。因此,迫切需要对Cell系中AlkBH7中AlkBH7的互乱和蛋白质组反应的研究。方法:在本研究中,通过免疫沉淀 - 质谱/质谱/质谱法(IP-MS / MS,研究了线粒体中AlkBH7的酰胺(IP-MS / MS) )。另外,我们建立了ALKBH7敲低和过表达细胞系,并进一步通过基于TMT的MS / MS在这些细胞系中鉴定了差异表达的蛋白质(DEP)。通过Western印迹分析验证了两种DEPS(UQCRH和HMGN1)。结果:通过生物信息分析蛋白质组学数据,我们发现ALKBH7参与蛋白质稳态和细胞免疫,以及通过调节通过调节细胞增殖,脂质代谢和编程坏死PTMA,PTM,UQCRH,HMGN1和HMGN2的表达。 AlkBH7的敲低导致UQCRH和HMGN1表达的上调,并且在ALKBH7过表达细胞系中检测到相反的表达模式;这些结果与我们的蛋白质组学数据一致。结论:我们的研究结果表明,UQCRH和HMGN1的表达由ALKBH7调节,这为未来的ALKBH7的研究提供了潜在的方向。此外,我们的结果还提供了综合了解与ALKBH7相关的分子机制和途径的洞察力。作者。 2019年。

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