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Nucleolar localization of phosphatidylinositol 4‐kinase PI4K230 in various mammalian cells

Background: Previous immunohistochemical investigations could not detect PI4K230, an isoform of mammalian phosphatidylinositol 4‐kinases (also called type III α), in the nucleus and nucleolus of cells in spite of its predicted nuclear localization signals. Methods: Immunofluorescent detection of PI4...

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Published in:Cytometry. Part A 2006-12, Vol.69A (12), p.1174-1183
Main Authors: Kakuk, Annamária, Friedländer, Elza, Vereb, György, Kása, Anita, Balla, András, Balla, Tamás, Heilmeyer, Ludwig M. G., Gergely, Pál
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Language:English
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Summary:Background: Previous immunohistochemical investigations could not detect PI4K230, an isoform of mammalian phosphatidylinositol 4‐kinases (also called type III α), in the nucleus and nucleolus of cells in spite of its predicted nuclear localization signals. Methods: Immunofluorescent detection of PI4K230 and other PI4K isoforms was performed on formaldehyde (PFA) or ethanol fixed cells and rat brain cryosections. Costaining with nucleolin and the effect of siRNA, Triton X‐100, DNase, and RNase treatments were also tested to determine the localization of PI4K230. Results: PI4K230 gives a prominent signal in the nucleolus of ethanol fixed rat brain cryosections and of several cell types in addition to its presence in the nucleus and cytoplasm. The PI4K230 immunoreactivity of the nucleolus is masked in PFA fixed cells, but it can be restored by treatment of PFA fixed cells with hot wet citrate buffer or by washing the cryosections with PBS prior to PFA fixation. Nucleolar PI4K230 occurs in a Triton X‐100 resistant complex. Treatment of COS‐7 cells with siRNA targeting PI4K230 and permeabilized B50 cells with DNase or RNase results in the loss of PI4K230 signal from the nucleolus. Conclusion: These experiments suggest the participation of PI4K230 in a DNase and RNase sensitive complex with a unique localization and function in the nucleolus. © 2006 International Society for Analytical Cytology
ISSN:1552-4922
1552-4930
DOI:10.1002/cyto.a.20347