The scaffold protein IQGAP1 links heat-induced stress signals to alternative splicing regulation in gastric cancer cells

被引:0
|
作者
Andrada-Maria Birladeanu
Malgorzata Rogalska
Myrto Potiri
Vasiliki Papadaki
Margarita Andreadou
Dimitris L. Kontoyiannis
Joe D. Lewis
Zoi Erpapazoglou
Panagiota Kafasla
机构
[1] B.S.R.C. “Alexander Fleming”,Institute for Fundamental Biomedical Research
[2] The Barcelona Institute of Science and Technology,Centre for Genomic Regulation (CRG)
[3] Universitat Pompeu Fabra (UPF),Department of Biology
[4] Aristotle University of Thessaloniki,undefined
[5] European Molecular Biology Laboratory,undefined
来源
Oncogene | 2021年 / 40卷
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摘要
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.
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页码:5518 / 5532
页数:14
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