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
关键词
D O I
暂无
中图分类号
学科分类号
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.
引用
收藏
页码:5518 / 5532
页数:14
相关论文
共 50 条
  • [1] The scaffold protein IQGAP1 links heat-induced stress signals to alternative splicing regulation in gastric cancer cells
    Birladeanu, Andrada-Maria
    Rogalska, Malgorzata
    Potiri, Myrto
    Papadaki, Vasiliki
    Andreadou, Margarita
    Kontoyiannis, Dimitris L.
    Lewis, Joe D.
    Erpapazoglou, Zoi
    Kafasla, Panagiota
    ONCOGENE, 2021, 40 (36) : 5518 - 5532
  • [2] RhoC protein stimulates migration of gastric cancer cells through interaction with scaffold protein IQGAP1
    Wu, Yan
    Chen, Yong-Chang
    Sang, Jian-Rong
    Xu, Wen-Rong
    MOLECULAR MEDICINE REPORTS, 2011, 4 (04) : 697 - 703
  • [3] Expression pattern of the scaffold protein IQGAP1 in lung cancer
    Nakamura, H
    Fujita, K
    Nakagawa, H
    Kishi, F
    Takeuchi, A
    Aute, I
    Kato, H
    ONCOLOGY REPORTS, 2005, 13 (03) : 427 - 431
  • [4] Regulation of Oncogenic Signaling Pathways in Hepatocellular Carcinoma by the Pleiotropic Scaffold Protein IQGAP1
    Delgado, E. R.
    Duncan, A. W.
    AMERICAN JOURNAL OF PATHOLOGY, 2017, 187 (10): : 2369 - 2370
  • [5] Menin represses the proliferation of gastric cancer cells by interacting with IQGAP1
    Ren, Feng
    Guo, Qin
    Zhou, Huan
    BIOMEDICAL REPORTS, 2023, 18 (04)
  • [6] RhoC Regulates the Proliferation of Gastric Cancer Cells through Interaction with IQGAP1
    Wu, Yan
    Tao, Yan
    Chen, Yongchang
    Xu, Wenrong
    PLOS ONE, 2012, 7 (11):
  • [7] IQGAP1 protein specifies amplifying cancer cells in glioblastoma multiforme
    Balenci, Laurent
    Clarke, Ian D.
    Dirks, Peter B.
    Assard, Nicole
    Ducray, Francois
    Jouvet, Anne
    Belin, Marie-Francoise
    Honnorat, Jerome
    Baudier, Jacques
    CANCER RESEARCH, 2006, 66 (18) : 9074 - 9082
  • [8] Local and non-local roles for the scaffold protein IQGAP1 in the regulation of epithelial cell junctions
    Schweikhard, V.
    Samson, E. B.
    Zimak, J.
    Diehl, M. R.
    MOLECULAR BIOLOGY OF THE CELL, 2015, 26
  • [9] Identification of IQGAP1, a Cdc42-interacting protein, in gastric parietal cells
    Rong, K
    Zhou, RH
    Wang, WX
    Watson, C
    Guo, Z
    Ammar, D
    Yao, XB
    MOLECULAR BIOLOGY OF THE CELL, 2001, 12 : 288A - 288A
  • [10] ROLE OF IQGAP1 IN HELICOBACTER PYLORI-INDUCED EPITHELIAL TO MESENCHYMAL TRANSITION OF GASTRIC EPITHELIAL CELLS
    Bessede, E.
    Staedel, C.
    Chambonnier, L.
    Megraud, F.
    Varon, C.
    HELICOBACTER, 2013, 18 : 150 - 151