Up-regulation of the KLF2 transcription factor by fluid shear stress requires nucleolin.
We have previously characterized the regulation of the KLF2 transcription factor gene by describing an induction complex that binds to and regulates its promoter. In the present study, by using DNA affinity chromatography and mass spectrometry, we have identified nucleolin as an additional protein that binds to a palindromic response ... region in the KLF2 promoter. The presence of nucleolin on the KLF2 promoter in macrophages was verified by electrophoretic mobility shift assays. Interestingly, in mouse and human endothelial cell lines, electrophoretic mobility shift assays and chromatin immunoprecipitation analyses indicated that nucleolin binds the KLF2 promoter only upon application of fluid shear stress. Pretreatment of the endothelial cells with LY294002, a specific inhibitor of phosphatidylinositol 3-kinase (PI3K), blocked the shear stress-induced binding of nucleolin to the promoter, demonstrating its PI3K-dependent regulation. Additionally, nucleolin exhibited dynamic flow-specific, PI3K-dependent alterations in size. Anti-nucleolin antibodies interacted with a 110-kDa form in static endothelial cells and with several catalytic forms that changed in abundance after the application of shear stress. Immunoprecipitation experiments demonstrated that fluid flow induced the interaction of nucleolin with the p85 regulatory subunit of PI3K. Finally, introduction of small interfering RNAs targeting the nucleolin genetic sequence selectively reduced nucleolin expression and was sufficient to block the induction of KLF2 by shear stress. These data support a general role for nucleolin in gene regulation and identify it as a novel factor involved in regulation of KLF2 expression.
Mesh Terms:
Amino Acid Sequence, Animals, Base Sequence, Binding Sites, Cell Line, Endothelium, Vascular, Humans, Kruppel-Like Transcription Factors, Macrophages, Mice, Phosphatidylinositol 3-Kinases, Phosphoproteins, Promoter Regions, Genetic, Protein Binding, RNA, Small Interfering, RNA-Binding Proteins, Rheology, Stress, Mechanical, Up-Regulation
Amino Acid Sequence, Animals, Base Sequence, Binding Sites, Cell Line, Endothelium, Vascular, Humans, Kruppel-Like Transcription Factors, Macrophages, Mice, Phosphatidylinositol 3-Kinases, Phosphoproteins, Promoter Regions, Genetic, Protein Binding, RNA, Small Interfering, RNA-Binding Proteins, Rheology, Stress, Mechanical, Up-Regulation
J. Biol. Chem.
Date: Jun. 02, 2006
PubMed ID: 16571724
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