Prahl Magdalena, Vilborg Anna, Palmberg Carina, Jörnvall Hans, Asker Charlotte, Wiman Klas G
Department of Oncology-Pathology, Cancer Center Karolinska, Karolinska Institutet, Stockholm, Sweden.
FEBS Lett. 2008 Jun 25;582(15):2173-7. doi: 10.1016/j.febslet.2008.04.065. Epub 2008 Jun 2.
The p53-induced Wig-1 gene encodes a double stranded RNA-binding zinc finger protein. We generated Saos-2 osteosarcoma cells expressing tetracycline-inducible Flag-tagged human Wig-1. Induction of Wig-1 expression by doxycycline inhibited cell growth in a long-term assay but did not cause any changes in cell cycle distribution nor increased fraction of apoptotic cells. Using co-immunoprecipitation and mass spectrometry, we identified two Wig-1-binding proteins, hnRNP A2/B1 and RNA Helicase A, both of which are involved in RNA processing. The binding was dependent on the presence of RNA. Our results establish a link between the p53 tumor suppressor and RNA processing via hnRNPA2/B1 and RNA Helicase A.
p53诱导的Wig-1基因编码一种双链RNA结合锌指蛋白。我们构建了表达四环素诱导型Flag标签人Wig-1的Saos-2骨肉瘤细胞。强力霉素诱导Wig-1表达在长期实验中抑制了细胞生长,但未引起细胞周期分布的任何变化,也未增加凋亡细胞比例。通过免疫共沉淀和质谱分析,我们鉴定出两种与Wig-1结合的蛋白,即hnRNP A2/B1和RNA解旋酶A,二者均参与RNA加工。这种结合依赖于RNA的存在。我们的结果通过hnRNPA2/B1和RNA解旋酶A建立了p53肿瘤抑制因子与RNA加工之间的联系。