Chromatin immunoprecipitation in M14 melanoma cells showed that the protein ERp57 (endoplasmic reticulum protein 57) binds to DNA in the proximity of STAT3 in a subset of STAT3-regulated genes. In the same cells, IL-6 induced a significant increase of the expression of one of these genes, i.e. CRP. Upon depletion of ERp57 by RNA interference. the phosphorylation of STAT3 on tyrosine 705 was decreased. and the IL-6-induced activation of CRP expression was completely suppressed. In vitro experiments showed that ERp57 is also required for the binding of STAT3 to its consensus sequence on DNA. Thus ERp57, previously shown to associate with STAT3 in the cytosol and in the nuclear STAT3-containing enhanceosome, is a necessary cofactor for the regulation of at least a subset of STAT3-dependent genes, probably intervening both at the site of STAT3 phosphorylation and at the nuclear level. (C) 2009 Elsevier Inc. All rights reserved.
Role of ERp57 in the signaling and transcriptional activity of STAT3 in a melanoma cell line / Chichiarelli, Silvia; Elisa, Gaucci; Ferraro, Anna; Grillo, Caterina; Altieri, Fabio; Cocchiola, Rossana; Valentina, Arcangeli; Turano, Carlo; Eufemi, Margherita. - In: ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS. - ISSN 0003-9861. - 494:2(2010), pp. 178-183. [10.1016/j.abb.2009.12.004]
Role of ERp57 in the signaling and transcriptional activity of STAT3 in a melanoma cell line
CHICHIARELLI, Silvia;FERRARO, Anna;GRILLO, CATERINA;ALTIERI, Fabio;COCCHIOLA, ROSSANA;TURANO, Carlo;EUFEMI, Margherita
2010
Abstract
Chromatin immunoprecipitation in M14 melanoma cells showed that the protein ERp57 (endoplasmic reticulum protein 57) binds to DNA in the proximity of STAT3 in a subset of STAT3-regulated genes. In the same cells, IL-6 induced a significant increase of the expression of one of these genes, i.e. CRP. Upon depletion of ERp57 by RNA interference. the phosphorylation of STAT3 on tyrosine 705 was decreased. and the IL-6-induced activation of CRP expression was completely suppressed. In vitro experiments showed that ERp57 is also required for the binding of STAT3 to its consensus sequence on DNA. Thus ERp57, previously shown to associate with STAT3 in the cytosol and in the nuclear STAT3-containing enhanceosome, is a necessary cofactor for the regulation of at least a subset of STAT3-dependent genes, probably intervening both at the site of STAT3 phosphorylation and at the nuclear level. (C) 2009 Elsevier Inc. All rights reserved.I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.
