http://www.cnr.it/ontology/cnr/individuo/prodotto/ID21184
Regulation of microRNA expression by HMGA1 proteins. (Articolo in rivista)
- Type
- Label
- Regulation of microRNA expression by HMGA1 proteins. (Articolo in rivista) (literal)
- Anno
- 2009-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1038/onc.2008.495 (literal)
- Alternative label
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- De Martino I; Visone R; Fedele M; Petrocca F; Palmieri D; Martinez Hoyos J; Forzati F; Croce CM; Fusco A. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
- Note
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Istituto di Endocrinologia ed Oncologia Sperimentale del CNR c/o Dipartimento di Biologia e Patologia Cellulare e Molecolare,
Facolta` di Medicina e Chirurgia di Napoli, Universita` degli Studi di Napoli 'Federico II', Naples, Italy; NOGEC (Naples
Oncogenomic Center)-CEINGE, Biotecnologie Avanzate-Napoli and SEMM--European School of Molecular Medicine--Naples
Site, Naples, Italy and Department of Molecular Virology, Immunology, and Medical Genetics, Comprehensive Cancer Center,
Ohio State University, Columbus, OH, USA (literal)
- Titolo
- Regulation of microRNA expression by HMGA1 proteins. (literal)
- Abstract
- The High Mobility Group proteins HMGA1 are nuclear
architectural factors that play a critical role in a wide
range of biological processes. Since recent studies have
identified the microRNAs (miRNAs) as important regulators
of gene expression, modulating critical cellular
functions suchas proliferation, apoptosis and differentiation,
the aim of our work was to identify the miRNAs that
are physiologically regulated by HMGA1 proteins. To
this purpose, we have analysed the miRNA expression
profile of mouse embryonic fibroblasts (MEFs) carrying
two, one or no Hmga1 functional alleles using a
microarray (miRNA microarray). By this approach, we
found a miRNA expression profile that differentiates
Hmga1-null MEFs from the wild-type ones. In particular,
a significant decrease in miR-196a-2, miR-101b, miR-331
and miR-29a was detected in homozygous Hmga1-knockout
MEFs in comparison withwi ld-type cells. Consistently,
these miRNAs are downregulated in most of the
analysed tissues of Hmga1-null mice in comparison with
the wild-type mice. ChIP assay shows that HMGA1 is
able to bind regions upstream of these miRNAs. Moreover,
we identified the HMGA2 gene product as a putative
target of miR-196a-2, suggesting that HMGA1 proteins
are able to downregulate the expression of the other
member of the HMGA family through the regulation of
the miR-196a-2 expression. Finally, ATXN1 and STC1
gene products have been identified as targets of miR-101b.
Therefore, it is reasonable to hypothesize that HMGA1
proteins are involved in several functions by regulating
miRNA expression. (literal)
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- Autore CNR
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