Kasyapa Chitta, Gu Ting-Lei, Nagarajan Lalitha, Polakiewicz Roberto, Cowell John K
Department of Medicine, Roswell Park Cancer Institute, Buffalo, NY, USA.
Proteomics. 2009 Aug;9(16):3979-88. doi: 10.1002/pmic.200800852.
The ZNF198-fibroblast growth factor receptor-1 (FGFR1) fusion kinase is a constitutively activated tyrosine kinase associated with a specific atypical myeloproliferative disease. The chimeric protein localizes to the cytoplasm, unlike the wild type FGFR1 receptor kinase, and presumably inappropriately phosphorylates specific targets as part of the oncogenic signaling cascade. Other than known targets of the FGFR1 kinase itself, few specific targets of ZNF198-FGFR1 have been identified. Using a genetically engineered HEK 293 cell system, we have identified proteins that are specifically phosphorylated in the presence of the fusion kinase using anti-phosphotyrosine immunoprecipitation and MS. Compared with 293 cells expressing exongenous wild type FGFR1, ZNF198-FGFR1 is associated with phosphorylation of several proteins including SSBP2, ABL, FLJ14235, CALM and TRIM4 proteins. The specificity of the phosphorylation events in the SSBP2 and ABL proteins, which have previously been implicated in leukemogenesis, was further confirmed independently using immunoprecipitation with protein-specific antibodies and Western blotting. The MS analysis also identified the phosphorylation events in the ZNF198 moiety in the chimeric protein that might be related to its function. These studies identify the intersection of several different leukemia-related pathways in the development of this myeloproliferative disorder and provide new insights into the substrates of FGFR1 under defined conditions.
锌指蛋白198-成纤维细胞生长因子受体1(FGFR1)融合激酶是一种组成性激活的酪氨酸激酶,与一种特定的非典型骨髓增殖性疾病相关。与野生型FGFR1受体激酶不同,嵌合蛋白定位于细胞质中,并且可能作为致癌信号级联反应的一部分不适当地磷酸化特定靶点。除了FGFR1激酶本身已知的靶点外,ZNF198-FGFR1的特定靶点很少被鉴定出来。利用基因工程的HEK 293细胞系统,我们通过抗磷酸酪氨酸免疫沉淀和质谱鉴定了在融合激酶存在下被特异性磷酸化的蛋白质。与表达外源野生型FGFR1的293细胞相比,ZNF198-FGFR1与包括SSBP2、ABL、FLJ14235、CALM和TRIM4蛋白在内的几种蛋白质的磷酸化有关。先前已证明与白血病发生有关的SSBP2和ABL蛋白中磷酸化事件的特异性,通过使用蛋白质特异性抗体进行免疫沉淀和蛋白质印迹进一步独立证实。质谱分析还确定了嵌合蛋白中ZNF198部分可能与其功能相关的磷酸化事件。这些研究确定了在这种骨髓增殖性疾病发展过程中几种不同白血病相关途径的交叉点,并为特定条件下FGFR1的底物提供了新的见解。