
Cytokine-induced apoptosis inhibitor 1 (CIAPIN1) is a newly identified anti-apoptotic molecule. Our previous studies have demonstrated that CIAPIN1 is ubiquitously expressed in normal fetal and adult human tissues and confers multidrug resistance in gastric cancer cells, possibly by upregulating the expression of multidrug resistance gene 1 and multidrug resistance-related protein 1. However, fundamental biological functions of CIAPIN1 have not been elucidated. In this study, we first predicted the subcellular localization of CIAPIN1 with bioinformatic approaches and then characterized the intracellular localization of CIAPIN1 in both human and mouse cells by a combination of techniques including (a) immunohistochemistry and immunofluorescence, (b) His-tagged CIAPIN1 expression, and (c) sub-cellular fractionation and analysis of CIAPIN1 in the fractions by Western blotting. All methods produced consistent results; CIAPIN1 was localized in both the cytoplasm and the nucleus and was accumulated in the nucleolus. Bioinformatic prediction disclosed a putative nuclear localization signal and a putative nuclear export signal within both human and mouse CIAPIN1. These findings suggest that CIAPIN1 may undergo a cytoplasm-nucleus-nucleolus translocation.
Cytoplasm, Blotting, Western, Intracellular Signaling Peptides and Proteins, Cell Fractionation, Immunohistochemistry, Sensitivity and Specificity, Cell Line, Mice, Organ Specificity, NIH 3T3 Cells, Animals, Humans, Cells, Cultured, In Situ Hybridization, Fluorescence, Subcellular Fractions
Cytoplasm, Blotting, Western, Intracellular Signaling Peptides and Proteins, Cell Fractionation, Immunohistochemistry, Sensitivity and Specificity, Cell Line, Mice, Organ Specificity, NIH 3T3 Cells, Animals, Humans, Cells, Cultured, In Situ Hybridization, Fluorescence, Subcellular Fractions
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