Functional impact of cancer-associated mutations in the tumor suppressor protein ING4.

Publisher: Irl Press At Oxford University Press Country of Publication: England NLM ID: 8008055 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2180 (Electronic) Linking ISSN: 01433334 NLM ISO Abbreviation: Carcinogenesis Subsets: MEDLINE

Publication: Oxford : Irl Press At Oxford University Press
Original Publication: [New York, IRL Press]

Cell Cycle Proteins/*genetics ; Homeodomain Proteins/*genetics ; Lung Neoplasms/*genetics ; Mutation/*genetics ; Sarcoma/*genetics ; Tumor Suppressor Proteins/*genetics; Animals ; Blotting, Western ; Cell Adhesion ; Cell Movement ; Cell Proliferation ; Cells, Cultured ; Endothelium, Vascular/cytology ; Endothelium, Vascular/metabolism ; Humans ; Lung Neoplasms/metabolism ; Lung Neoplasms/pathology ; Mice ; Mutagenesis, Site-Directed ; NIH 3T3 Cells ; Protein Conformation ; RNA, Messenger/genetics ; Reverse Transcriptase Polymerase Chain Reaction ; Sarcoma/metabolism ; Sarcoma/pathology ; Subcellular Fractions

Inhibitor of growth 4 (ING4) is a member of the ING family of tumor suppressor proteins. In this study, we have analyzed the impact of two mutations in ING4 associated with human tumors (Y121N and N214D), testing their behavior in a series of functional, biochemical and structural analyses. We report that the N214D mutation dramatically dampened the ability of ING4 to inhibit proliferation, anchorage-independent growth or cell migration or to sensitize to cell death. In turn, the Y121N mutant did not differ significantly from wild-type ING4 in our assays. Neither of the mutations altered the normal subcellular localization of ING4, showing predominantly nuclear accumulation. We investigated the molecular basis of the defect in the activity of the N214D mutant. The folding and ability to bind histone marks of ING4 was not significantly altered by this mutation. Instead, we found that the functional impairment of the N214D mutant correlates with reduced protein stability due to increased proteasome-mediated degradation. In summary, our data demonstrates that a point mutation of ING4 associated to human tumors leads to the loss of several essential functions of ING4 pertinent to tumor protection and highlight the importance of ING4 function to prevent tumorigenesis.

0 (Cell Cycle Proteins)
0 (Homeodomain Proteins)
0 (ING4 protein, human)
0 (RNA, Messenger)
0 (Tumor Suppressor Proteins)

Date Created: 20100814 Date Completed: 20101116 Latest Revision: 20101101

20221213

10.1093/carcin/bgq171

20705953