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   <dc:title>MicroRNA-322 (miR-322) and its target protein Tob2 modulate Osterix (Osx) mRNA stability</dc:title>
   <dc:creator>Gamez Molina, Beatriz</dc:creator>
   <dc:creator>Rodríguez Carballo, Edgardo</dc:creator>
   <dc:creator>Bartrons Bach, Ramon</dc:creator>
   <dc:creator>Rosa López, José Luis</dc:creator>
   <dc:creator>Ventura Pujol, Francesc</dc:creator>
   <dc:subject>Cicle cel·lular</dc:subject>
   <dc:subject>Expressió gènica</dc:subject>
   <dc:subject>Citologia</dc:subject>
   <dc:subject>Factors de transcripció</dc:subject>
   <dc:subject>Cell cycle</dc:subject>
   <dc:subject>Gene expression</dc:subject>
   <dc:subject>Cytology</dc:subject>
   <dc:subject>Transcription factors</dc:subject>
   <dcterms:abstract>Osteogenesis depends on a coordinated network of signals and transcription factors such as Runx2 and Osterix. Recent evidence indicates that microRNAs (miRNAs) act as important post-transcriptional regulators in a large number of processes, including osteoblast differentiation. In this study, we performed miRNA expression profiling and identified miR-322, a BMP-2-down-regulated miRNA, as a regulator of osteoblast differentiation. We report miR-322 gain- and loss-of-function experiments in C2C12 and MC3T3-E1 cells and primary cultures of murine bone marrow-derived mesenchymal stem cells. We demonstrate that overexpression of miR-322 enhances BMP-2 response, increasing the expression of Osx and other osteogenic genes. Furthermore, we identify Tob2 as a target of miR-322, and we characterize the specific Tob2 3′-UTR sequence bound by miR-322 by reporter assays. We demonstrate that Tob2 is a negative regulator of osteogenesis that binds and mediates degradation of Osx mRNA. Our results demonstrate a new molecular mechanism controlling osteogenesis through the specific miR-322/Tob2 regulation of specific target mRNAs. This regulatory circuit provides a clear example of a complex miRNA-transcription factor network for fine-tuning the osteoblast differentiation program.</dcterms:abstract>
   <dcterms:issued>2021-05-18T11:51:57Z</dcterms:issued>
   <dcterms:issued>2021-05-18T11:51:57Z</dcterms:issued>
   <dcterms:issued>2013-05-17</dcterms:issued>
   <dcterms:issued>2021-05-18T11:51:57Z</dcterms:issued>
   <dc:type>info:eu-repo/semantics/article</dc:type>
   <dc:type>info:eu-repo/semantics/publishedVersion</dc:type>
   <dc:relation>Reproducció del document publicat a: https://doi.org/10.1074/jbc.M112.432104</dc:relation>
   <dc:relation>Journal of Biological Chemistry, 2013, vol. 288, num. 20, p. 14264-14275</dc:relation>
   <dc:relation>https://doi.org/10.1074/jbc.M112.432104</dc:relation>
   <dc:rights>(c) American Society for Biochemistry and Molecular Biology, 2013</dc:rights>
   <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
   <dc:publisher>American Society for Biochemistry and Molecular Biology</dc:publisher>
   <dc:source>Articles publicats en revistes (Ciències Fisiològiques)</dc:source>
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