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Loss of MTG16a (CBFA2T3), a novel rDNA repressor, leads to increased ribogenesis and disruption of breast acinar morphogenesis

Human MTG16a (CBFA2T3), a chromatin repressor with nucleolar localization, was described to act as a suppressor of breast tumourigenesis. Here we show that MTG16a is a novel ribosomal gene repressor, which can counteract MYC-driven activation of ribosomal RNA (rRNA) transcription. We also show that...

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Detalles Bibliográficos
Autores principales: Rossetti, Stefano, Hoogeveen, André T, Esposito, Joseph, Sacchi, Nicoletta
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3828852/
https://www.ncbi.nlm.nih.gov/pubmed/19961547
http://dx.doi.org/10.1111/j.1582-4934.2009.00982.x
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author Rossetti, Stefano
Hoogeveen, André T
Esposito, Joseph
Sacchi, Nicoletta
author_facet Rossetti, Stefano
Hoogeveen, André T
Esposito, Joseph
Sacchi, Nicoletta
author_sort Rossetti, Stefano
collection PubMed
description Human MTG16a (CBFA2T3), a chromatin repressor with nucleolar localization, was described to act as a suppressor of breast tumourigenesis. Here we show that MTG16a is a novel ribosomal gene repressor, which can counteract MYC-driven activation of ribosomal RNA (rRNA) transcription. We also show that either knocking down MTG16a by RNA interference, or sequestering MTG16a outside the nucleolus of human breast epithelial cells, hampers acinar morphogenesis concomitant with up-regulation of rRNA synthesis and increased ribogenesis. This is the first demonstration that loss of MTG16a function in the nucleolus of breast epithelial cells can induce morphological and molecular changes typical of breast cancer initiation.
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spelling pubmed-38288522015-04-20 Loss of MTG16a (CBFA2T3), a novel rDNA repressor, leads to increased ribogenesis and disruption of breast acinar morphogenesis Rossetti, Stefano Hoogeveen, André T Esposito, Joseph Sacchi, Nicoletta J Cell Mol Med Articles Human MTG16a (CBFA2T3), a chromatin repressor with nucleolar localization, was described to act as a suppressor of breast tumourigenesis. Here we show that MTG16a is a novel ribosomal gene repressor, which can counteract MYC-driven activation of ribosomal RNA (rRNA) transcription. We also show that either knocking down MTG16a by RNA interference, or sequestering MTG16a outside the nucleolus of human breast epithelial cells, hampers acinar morphogenesis concomitant with up-regulation of rRNA synthesis and increased ribogenesis. This is the first demonstration that loss of MTG16a function in the nucleolus of breast epithelial cells can induce morphological and molecular changes typical of breast cancer initiation. Blackwell Publishing Ltd 2010-06 2009-12-02 /pmc/articles/PMC3828852/ /pubmed/19961547 http://dx.doi.org/10.1111/j.1582-4934.2009.00982.x Text en © 2009 The Authors Journal compilation © 2010 Foundation for Cellular and Molecular Medicine/Blackwell Publishing Ltd
spellingShingle Articles
Rossetti, Stefano
Hoogeveen, André T
Esposito, Joseph
Sacchi, Nicoletta
Loss of MTG16a (CBFA2T3), a novel rDNA repressor, leads to increased ribogenesis and disruption of breast acinar morphogenesis
title Loss of MTG16a (CBFA2T3), a novel rDNA repressor, leads to increased ribogenesis and disruption of breast acinar morphogenesis
title_full Loss of MTG16a (CBFA2T3), a novel rDNA repressor, leads to increased ribogenesis and disruption of breast acinar morphogenesis
title_fullStr Loss of MTG16a (CBFA2T3), a novel rDNA repressor, leads to increased ribogenesis and disruption of breast acinar morphogenesis
title_full_unstemmed Loss of MTG16a (CBFA2T3), a novel rDNA repressor, leads to increased ribogenesis and disruption of breast acinar morphogenesis
title_short Loss of MTG16a (CBFA2T3), a novel rDNA repressor, leads to increased ribogenesis and disruption of breast acinar morphogenesis
title_sort loss of mtg16a (cbfa2t3), a novel rdna repressor, leads to increased ribogenesis and disruption of breast acinar morphogenesis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3828852/
https://www.ncbi.nlm.nih.gov/pubmed/19961547
http://dx.doi.org/10.1111/j.1582-4934.2009.00982.x
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