the role of mir-103 and mir-107 in regulation of cdk5r1 expression and in cellular migrationmir - 103的作用,mir - 107 cdk5r1表达的调控和细胞迁移.pdfVIP

the role of mir-103 and mir-107 in regulation of cdk5r1 expression and in cellular migrationmir - 103的作用,mir - 107 cdk5r1表达的调控和细胞迁移.pdf

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The Role of miR-103 and miR-107 in Regulation of CDK5R1 Expression and in Cellular Migration 1 2 1 3,4 3 Silvia Moncini , Alessandro Salvi , Paola Zuccotti , Gabriella Viero , Alessandro Quattrone , Sergio 2 2 1 1 Barlati , Giuseppina De Petro , Marco Venturin , Paola Riva * 1 Department of Biology and Genetics for Medical Sciences, University of Milan, Milan, Italy, 2 Division of Biology and Genetics, Department of Biomedical Sciences and Biotechnology, University of Brescia, Brescia, Italy, 3 Centre for Integrative Biology (CIBIO), University of Trento, Trento, Italy, 4 Institute of Biophysics, National Research Council, Trento, Italy Abstract CDK5R1 encodes p35, a specific activator of the serine/threonine kinase CDK5, which plays crucial roles in CNS development and maintenance. CDK5 activity strongly depends on p35 levels and p35/CDK5 misregulation is deleterious for correct CNS function, suggesting that a tightly controlled regulation of CDK5R1 expression is needed for proper CDK5 activity. Accordingly, CDK5R1 expression was demonstrated to be controlled at both transcriptional and post-transcriptional levels, but a possible regulation through microRNAs (miRNAs) has never been investigated. We predicted, within the large CDK5R1 39UTR several miRNA target sites. Among them, we selected for functional studies miR-103 and miR-107, whose expression has shown a strong inverse correlation with p35 levels in different cell lines. A significant reduction of CDK5R1 mRNA and p35 levels was observed after transfection of SK-N-BE neuroblastoma cells with the miR-103 or miR-107 precursor (pre-miR- 1

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