Cyclin D1 is a NF-B corepressor

P. N. FERNÁNDEZ LARROSA; M.F. RUBIO; C. ALVARADO; L. PANELO; M. RUIZ GRECCO; G. COLO; G. MARTINEZ NOEL; S. MICENMACHER; M. COSTAS

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH

ELSEVIER SCIENCE BV

Año: 2012 p. 1119 - 1131

0167-4889

F.Rubio y PN Fernandez Larrosa son ambos primeros autores.NF-êB regulates the expression of Cyclin D1 (CD1), while RAC3 is an NF-êB coactivator that enhances its transcriptional activity. In this work, we investigated the regulatory role of CD1 on NF-êB activity. We found that CD1 inhibits NF-êB transcriptional activity through a corepressor function that can be reverted by over-expressing RAC3. In both, tumoral and non-tumoral cells, the expression pattern of RAC3 and CD1 is regulated by the cell cycle, showing a gap between the maximal expression levels of each protein. The individual increase, by transfection, of either CD1 or RAC3 enhances cell proliferation. However the simultaneous and constitutive over-expression of both proteins has an inhibitory effect. Our results suggest that the relative amounts of CD1 and RAC3, and the timing of expression of these oncogenes could tilt the balance of tumor cell proliferation in response to external signals.