Loading…

CBX7 gene expression plays a negative role in adipocyte cell growth and differentiation

We have recently generated knockout mice for the Cbx7 gene, coding for a polycomb group protein that is downregulated in human malignant neoplasias. These mice develop liver and lung adenomas and carcinomas, which confirms a tumour suppressor role for CBX7. The CBX7 ability to downregulate CCNE1 exp...

Full description

Saved in:
Bibliographic Details
Published in:Biology open 2014-09, Vol.3 (9), p.871-879
Main Authors: Forzati, Floriana, Federico, Antonella, Pallante, Pierlorenzo, Colamaio, Marianna, Esposito, Francesco, Sepe, Romina, Gargiulo, Sara, Luciano, Antonio, Arra, Claudio, Palma, Giuseppe, Bon, Giulia, Bucher, Stefania, Falcioni, Rita, Brunetti, Arturo, Battista, Sabrina, Fedele, Monica, Fusco, Alfredo
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary:We have recently generated knockout mice for the Cbx7 gene, coding for a polycomb group protein that is downregulated in human malignant neoplasias. These mice develop liver and lung adenomas and carcinomas, which confirms a tumour suppressor role for CBX7. The CBX7 ability to downregulate CCNE1 expression likely accounts for the phenotype of the Cbx7-null mice. Unexpectedly, Cbx7-knockout mice had a higher fat tissue mass than wild-type, suggesting a role of CBX7 in adipogenesis. Consistently, we demonstrate that Cbx7-null mouse embryonic fibroblasts go towards adipocyte differentiation more efficiently than their wild-type counterparts, and this effect is Cbx7 dose-dependent. Similar results were obtained when Cbx7-null embryonic stem cells were induced to differentiate into adipocytes. Conversely, mouse embryonic fibroblasts and human adipose-derived stem cells overexpressing CBX7 show an opposite behaviour. These findings support a negative role of CBX7 in the control of adipocyte cell growth and differentiation.
ISSN:2046-6390
2046-6390
DOI:10.1242/bio.20147872