Tariki Melanie, Wieczorek Sarah Alexandra, Schneider Philipp, Bänfer Sebastian, Veitinger Sophie, Jacob Ralf, Fendrich Volker, Lauth Matthias
Philipps University, Institute of Molecular Biology and Tumor Research (IMT), Emil-Mannkopff-Str. 2, 35037 Marburg, Germany.
Cell Signal. 2013 Dec;25(12):2668-75. doi: 10.1016/j.cellsig.2013.08.037. Epub 2013 Sep 7.
Suppressor of fused (SUFU) is an essential negative regulator of the mammalian Hedgehog (HH) signaling pathway and its loss is associated with cancer development. On a cellular level, endogenous SUFU can mainly be detected in the cytoplasm and the nucleus. However, immunostaining of pancreatic cancer specimen revealed the existence of cell types showing selective enrichment of endogenous SUFU in the nucleus. Following up on this observation, we found that a SUFU construct which was experimentally tethered exclusively to the nucleus was unable to antagonize endogenous HH signaling, in contrast to control SUFU. These data suggest that alterations in the normal subcellular distribution of SUFU might interfere with its established negative role on the HH pathway. Performing a multi-well kinase screen in human cells identified RIO kinase 3 (RIOK3) as a novel modulator of SUFU subcellular distribution. Functionally, RIOK3 acts as a SUFU-dependent positive regulator of HH signaling. Taken together, we propose that factors modulating the nucleo-cytoplasmic distribution of SUFU impact on the normal function of this tumor suppressing protein.
融合抑制因子(SUFU)是哺乳动物刺猬索尼克(HH)信号通路中一种重要的负调节因子,其缺失与癌症发展相关。在细胞水平上,内源性SUFU主要可在细胞质和细胞核中检测到。然而,胰腺癌标本的免疫染色显示存在一些细胞类型,其细胞核内有内源性SUFU的选择性富集。基于这一观察结果,我们发现,与对照SUFU相比,实验性地仅与细胞核相连的SUFU构建体无法拮抗内源性HH信号。这些数据表明,SUFU正常亚细胞分布的改变可能会干扰其在HH信号通路上已确立的负性作用。在人类细胞中进行的多孔激酶筛选确定RIO激酶3(RIOK3)是SUFU亚细胞分布的新型调节因子。在功能上,RIOK3作为HH信号的SUFU依赖性正调节因子发挥作用。综上所述,我们提出调节SUFU核质分布的因子会影响这种肿瘤抑制蛋白的正常功能。