Turku Bioscience Centre, University of Turku and Åbo Akademi University, 20500 Turku, Finland; Institute of Biomedicine, University of Turku, 20500 Turku, Finland; TuBS and TuDMM Doctoral Programmes, University of Turku, 20500 Turku, Finland.
Turku Bioscience Centre, University of Turku and Åbo Akademi University, 20500 Turku, Finland.
J Biol Chem. 2020 Mar 27;295(13):4194-4211. doi: 10.1074/jbc.RA119.011265. Epub 2020 Feb 18.
Protein phosphatase 2A (PP2A) critically regulates cell signaling and is a human tumor suppressor. PP2A complexes are modulated by proteins such as cancerous inhibitor of protein phosphatase 2A (CIP2A), protein phosphatase methylesterase 1 (PME-1), and SET nuclear proto-oncogene (SET) that often are deregulated in cancers. However, how they impact cellular phosphorylation and how redundant they are in cellular regulation is poorly understood. Here, we conducted a systematic phosphoproteomics screen for phosphotargets modulated by siRNA-mediated depletion of CIP2A, PME-1, and SET (to reactivate PP2A) or the scaffolding A-subunit of PP2A (PPP2R1A) (to inhibit PP2A) in HeLa cells. We identified PP2A-modulated targets in diverse cellular pathways, including kinase signaling, cytoskeleton, RNA splicing, DNA repair, and nuclear lamina. The results indicate nonredundancy among CIP2A, PME-1, and SET in phosphotarget regulation. Notably, PP2A inhibition or reactivation affected largely distinct phosphopeptides, introducing a concept of nonoverlapping phosphatase inhibition- and activation-responsive sites (PIRS and PARS, respectively). This phenomenon is explained by the PPP2R1A inhibition impacting primarily dephosphorylated threonines, whereas PP2A reactivation results in dephosphorylation of clustered and acidophilic sites. Using comprehensive drug-sensitivity screening in PP2A-modulated cells to evaluate the functional impact of PP2A across diverse cellular pathways targeted by these drugs, we found that consistent with global phosphoproteome effects, PP2A modulations broadly affect responses to more than 200 drugs inhibiting a broad spectrum of cancer-relevant targets. These findings advance our understanding of the phosphoproteins, pharmacological responses, and cellular processes regulated by PP2A modulation and may enable the development of combination therapies.
蛋白磷酸酶 2A(PP2A)对细胞信号转导具有关键调节作用,是一种人类肿瘤抑制因子。PP2A 复合物受蛋白的调节,如癌性蛋白磷酸酶 2A 抑制剂(CIP2A)、蛋白磷酸酶甲硫氨酸酯酶 1(PME-1)和 SET 核原癌基因(SET),这些蛋白在癌症中经常失调。然而,它们如何影响细胞磷酸化以及它们在细胞调节中的冗余程度尚不清楚。在这里,我们通过 siRNA 介导的 CIP2A、PME-1 和 SET(重新激活 PP2A)或 PP2A 支架 A 亚基(PPP2R1A)(抑制 PP2A)耗竭的细胞进行了系统的磷酸蛋白质组学筛选,以鉴定 HeLa 细胞中受调控的磷酸化靶点。我们在多种细胞途径中鉴定了 PP2A 调控的靶点,包括激酶信号转导、细胞骨架、RNA 剪接、DNA 修复和核层。结果表明,CIP2A、PME-1 和 SET 在磷酸化靶点调控中没有冗余。值得注意的是,PP2A 抑制或重新激活主要影响不同的磷酸肽,引入了非重叠的磷酸酶抑制和激活响应位点(PIRS 和 PARS)的概念。这种现象可以通过 PPP2R1A 抑制主要影响去磷酸化的苏氨酸来解释,而 PP2A 再激活导致簇集和酸性位点去磷酸化。通过对受 PP2A 调节的细胞进行全面的药物敏感性筛选,评估这些药物靶向的多种细胞途径中 PP2A 的功能影响,我们发现,与全局磷酸蛋白质组学效应一致,PP2A 调节广泛影响对 200 多种药物的反应,这些药物抑制广泛的与癌症相关的靶点。这些发现提高了我们对受 PP2A 调节的磷酸蛋白质、药理反应和细胞过程的理解,并可能为组合疗法的发展提供依据。