Institute for Fundamental Biomedical Research, B.S.R.C. "Alexander Fleming", 34 Fleming st. 16672 Vari, Athens, Greece.
Centre for Genomic Regulation (CRG), The Barcelona Institute of Science and Technology, Dr Aiguader 88, Barcelona, 08003, Spain.
Oncogene. 2021 Sep;40(36):5518-5532. doi: 10.1038/s41388-021-01963-7. Epub 2021 Jul 23.
In response to oncogenic signals, Alternative Splicing (AS) regulators such as SR and hnRNP proteins show altered expression levels, subnuclear distribution and/or post-translational modification status, but the link between signals and these changes remains unknown. Here, we report that a cytosolic scaffold protein, IQGAP1, performs this task in response to heat-induced signals. We show that in gastric cancer cells, a nuclear pool of IQGAP1 acts as a tethering module for a group of spliceosome components, including hnRNPM, a splicing factor critical for the response of the spliceosome to heat-shock. IQGAP1 controls hnRNPM's sumoylation, subnuclear localisation and the relevant response of the AS machinery to heat-induced stress. Genome-wide analyses reveal that IQGAP1 and hnRNPM co-regulate the AS of a cell cycle-related RNA regulon in gastric cancer cells, thus favouring the accelerated proliferation phenotype of gastric cancer cells. Overall, we reveal a missing link between stress signals and AS regulation.
针对致癌信号,剪接调控因子(如 SR 和 hnRNP 蛋白)表现出表达水平、亚核分布和/或翻译后修饰状态的改变,但信号与这些变化之间的联系仍不清楚。在这里,我们报告细胞溶质支架蛋白 IQGAP1 响应热诱导信号执行此任务。我们表明,在胃癌细胞中,IQGAP1 的核池作为一组剪接体成分(包括 hnRNPM)的连接模块,hnRNPM 是剪接体对热休克反应的关键剪接因子。IQGAP1 控制 hnRNPM 的 SUMO 化、亚核定位以及剪接体机制对热诱导应激的相应反应。全基因组分析表明,IQGAP1 和 hnRNPM 共同调节胃癌细胞中与细胞周期相关的 RNA 调控子的 AS,从而有利于胃癌细胞的加速增殖表型。总的来说,我们揭示了应激信号与 AS 调控之间缺失的联系。