2014•Jiguang shengwu xuebaoRequires access

The Role of miR-223 on PAX6 Gene 3'-Untranslated Region in Glioblastoma Cells

Luo Qizh

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Abstract

Objective: To identify the regulation of miR-223 to PAX6 gene 3'-UTR in glioblastoma cells. Methods:Bioinformatics software was applied to predict the PAX6 3'-UTR targeting miRNAs. The wild type and mutation type of PAX6 gene 3'-UTR luciferase vectors were constructed respectively. The dual luciferase assay system was used to detect the reporter activity followed by co-transfecting the luciferase vector constructed and miR-223 mimics into U251 cells.Results: Bioinformatics software prediction results showed that PAX6 may be a target of miR-223. The luciferase assay revealed that miR-223 mimics could significantly decrease the luciferase activity of wild type PAX6 3'-UTR plasmid,compared with the wild type and mutation plasmid transfection group,respectively. Conclusion: miR-223 could negatively target and regulate the activity of PAX6 gene 3'-UTR.

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What this paper is about

Objective: To identify the regulation of miR-223 to PAX6 gene 3'-UTR in glioblastoma cells. Methods:Bioinformatics software was applied to predict the PAX6 3'-UTR targeting miRNAs. The wild type and mutation type of PAX6 gene 3'-UTR luciferase vectors were constructed respectively. The dual luciferase assay system was used to detect the reporter activity followed by co-transfecting the luciferase vector constructed and miR-223 mimics into U251 cells.Results: Bioinformatics software prediction results showed that PAX6 may be a target of miR-223. The luciferase assay revealed that miR-223 mimics could significantly decrease the luciferase activity of wild type PAX6 3'-UTR plasmid,compared with the wild type and mutation plasmid transfection group,respectively. Conclusion: miR-223 could negatively target and regulate the activity of PAX6 gene 3'-UTR.

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Available abstract

Objective: To identify the regulation of miR-223 to PAX6 gene 3'-UTR in glioblastoma cells. Methods:Bioinformatics software was applied to predict the PAX6 3'-UTR targeting miRNAs. The wild type and mutation type of PAX6 gene 3'-UTR luciferase vectors were constructed respectively. The dual luciferase assay system was used to detect the reporter activity followed by co-transfecting the luciferase vector constructed and miR-223 mimics into U251 cells.Results: Bioinformatics software prediction results showed that PAX6 may be a target of miR-223. The luciferase assay revealed that miR-223 mimics could significantly decrease the luciferase activity of wild type PAX6 3'-UTR plasmid,compared with the wild type and mutation plasmid transfection group,respectively. Conclusion: miR-223 could negatively target and regulate the activity of PAX6 gene 3'-UTR.

Key concepts: PAX6, Luciferase, Transfection, Three prime untranslated region, Gene, Untranslated region, microRNA, Reporter gene

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