[KIT的D816V突变在COS-1细胞中特异性诱导HNRNPL和HNRNPK磷酸化]。

Liangying Zhang, Shaoting Zhang, Zhaoyang Fan, Zongying Jiang, Shujing Li, Anbu Liu, Jianmin Sun
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引用次数: 0

摘要

目的研究III酪氨酸激酶受体KIT D816V突变对RNA结合蛋白HNRNPL和HNRNPK的调控作用。方法在COS-1细胞中单独或与HNRNPL或HNRNPK联合表达野生型KIT或KIT D816V突变。免疫沉淀和Western blot检测KIT的激活、HNRNPL和HNRNPK的磷酸化水平。用共聚焦显微镜检测COS-1细胞中KIT、HNRNPL和HNRNPK的定位。结果野生型KIT需要结合其配体干细胞因子(SCF)磷酸化,而KIT D816V无需SCF刺激即可自动磷酸化。此外,KIT D816V可以诱导HNRNPL和HNRNPK磷酸化,这在野生型KIT中是不可能的。HNRNPL和HNRNPK在细胞核中表达,野生型KIT在细胞质和细胞膜中表达,KIT D816V主要存在于细胞质中。结论野生型KIT需要SCF结合才能激活,而KIT D816V无需SCF刺激即可自动激活,并特异性诱导HNRNPL和HNRNPK磷酸化。
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[D816V mutation of KIT specifically induces phosphorylation of HNRNPL and HNRNPK in COS-1 cells].

Objective To study the regulation of D816V mutation of III tyrosine kinase receptor KIT on RNA binding proteins HNRNPL and HNRNPK. Methods In COS-1 cells, wild-type KIT or KIT D816V mutation were expressed alone or together with HNRNPL or HNRNPK. Activation of KIT and phosphorylation of HNRNPL and HNRNPK were detected by immunoprecipitation and Western blot analysis. The localization of KIT, HNRNPL and HNRNPK in COS-1 cells were examined by confocal microscopy. Results Wild-type KIT needs to bind its ligand stem cell factor (SCF) for phosphorylation, while KIT D816V could auto-phosphorylation without SCF stimulation. In addition, KIT D816V can induce phosphorylation of HNRNPL and HNRNPK, which is not possible in wild-type KIT. HNRNPL and HNRNPK are expressed in the nucleus, and wild-type KIT is expressed in cytosol and cell membrane, while KIT D816V is mainly found in cytosol. Conclusion Wild-type KIT needs SCF binding for activation, while KIT D816V can autoactivate without SCF stimulation, and induces phosphorylation of HNRNPL and HNRNPK specifically.

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