Decreased expression of BRCA1 in SK-BR-3 cells is the result of aberrant activation of the GABP Beta promoter by an NRF-1-containing complex

<p>Abstract</p> <p>Background</p> <p>BRCA1 has recently been identified as a potential regulator of mammary stem/progenitor cell differentiation, and this function may explain the high prevalence of breast cancer in <it>BRCA1 </it>mutation carriers, as well...

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Main Authors: MacDonald Gwen, Thompson Crista, Mueller Christopher R
Format: Article
Language:English
Published: BMC 2011-05-01
Series:Molecular Cancer
Online Access:http://www.molecular-cancer.com/content/10/1/62
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author MacDonald Gwen
Thompson Crista
Mueller Christopher R
author_facet MacDonald Gwen
Thompson Crista
Mueller Christopher R
author_sort MacDonald Gwen
collection DOAJ
description <p>Abstract</p> <p>Background</p> <p>BRCA1 has recently been identified as a potential regulator of mammary stem/progenitor cell differentiation, and this function may explain the high prevalence of breast cancer in <it>BRCA1 </it>mutation carriers, as well as the downregulation of BRCA1 in a large proportion of sporadic breast cancers. That is, loss of BRCA1 function results in blocked differentiation with expansion of the mammary stem/progenitor cells. Because BRCA1 also maintains genomic integrity, its loss could produce a pool of genetically unstable stem/progenitor cells that are prime targets for further transforming events. Thus, elucidating the regulatory mechanisms of <it>BRCA1 </it>expression is important to our understanding of normal and malignant breast differentiation.</p> <p>Results</p> <p>Loss of BRCA1 expression in the ErbB2-amplified SK-BR-3 cell line was found to be the result of loss of activity of the <it>ets </it>transcription factor GABP, a previously characterized regulator of BRCA1 transcription. The expression of the non-DNA binding GABPβ subunit was shown to be deficient, while the DNA binding subunit, GABPα was rendered unstable by the absence of GABPβ. Deletion analysis of the GABPβ proximal promoter identified a potential NRF-1 binding site as being critical for expression. Supershift analysis, the binding of recombinant protein and chromatin immunoprecipitation confirmed the role of NRF-1 in regulating the expression of GABPβ. The siRNA knockdown of NRF-1 resulted in decreased GABPβ and BRCA1 expression in MCF-7 cells indicating that they form a transcriptional network. NRF-1 levels and activity did not differ between SK-BR-3 and MCF-7 cells, however the NRF-1 containing complex on the GABPβ promoter differed between the two lines and appears to be the result of altered coactivator binding.</p> <p>Conclusions</p> <p>Both NRF-1 and GABP have been linked to the regulation of nuclear-encoded mitochondrial proteins, and the results of this study suggest their expression is coordinated by NRF-1's activation of the GABPβ promoter. Their linkage to BRCA1, a potential breast stem cell regulator, implies a connection between the induction of mitochondrial metabolism and breast differentiation.</p>
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spelling doaj.art-3c61ec494fff4fe8bcc612cca7c538972022-12-21T19:11:32ZengBMCMolecular Cancer1476-45982011-05-011016210.1186/1476-4598-10-62Decreased expression of BRCA1 in SK-BR-3 cells is the result of aberrant activation of the GABP Beta promoter by an NRF-1-containing complexMacDonald GwenThompson CristaMueller Christopher R<p>Abstract</p> <p>Background</p> <p>BRCA1 has recently been identified as a potential regulator of mammary stem/progenitor cell differentiation, and this function may explain the high prevalence of breast cancer in <it>BRCA1 </it>mutation carriers, as well as the downregulation of BRCA1 in a large proportion of sporadic breast cancers. That is, loss of BRCA1 function results in blocked differentiation with expansion of the mammary stem/progenitor cells. Because BRCA1 also maintains genomic integrity, its loss could produce a pool of genetically unstable stem/progenitor cells that are prime targets for further transforming events. Thus, elucidating the regulatory mechanisms of <it>BRCA1 </it>expression is important to our understanding of normal and malignant breast differentiation.</p> <p>Results</p> <p>Loss of BRCA1 expression in the ErbB2-amplified SK-BR-3 cell line was found to be the result of loss of activity of the <it>ets </it>transcription factor GABP, a previously characterized regulator of BRCA1 transcription. The expression of the non-DNA binding GABPβ subunit was shown to be deficient, while the DNA binding subunit, GABPα was rendered unstable by the absence of GABPβ. Deletion analysis of the GABPβ proximal promoter identified a potential NRF-1 binding site as being critical for expression. Supershift analysis, the binding of recombinant protein and chromatin immunoprecipitation confirmed the role of NRF-1 in regulating the expression of GABPβ. The siRNA knockdown of NRF-1 resulted in decreased GABPβ and BRCA1 expression in MCF-7 cells indicating that they form a transcriptional network. NRF-1 levels and activity did not differ between SK-BR-3 and MCF-7 cells, however the NRF-1 containing complex on the GABPβ promoter differed between the two lines and appears to be the result of altered coactivator binding.</p> <p>Conclusions</p> <p>Both NRF-1 and GABP have been linked to the regulation of nuclear-encoded mitochondrial proteins, and the results of this study suggest their expression is coordinated by NRF-1's activation of the GABPβ promoter. Their linkage to BRCA1, a potential breast stem cell regulator, implies a connection between the induction of mitochondrial metabolism and breast differentiation.</p>http://www.molecular-cancer.com/content/10/1/62
spellingShingle MacDonald Gwen
Thompson Crista
Mueller Christopher R
Decreased expression of BRCA1 in SK-BR-3 cells is the result of aberrant activation of the GABP Beta promoter by an NRF-1-containing complex
Molecular Cancer
title Decreased expression of BRCA1 in SK-BR-3 cells is the result of aberrant activation of the GABP Beta promoter by an NRF-1-containing complex
title_full Decreased expression of BRCA1 in SK-BR-3 cells is the result of aberrant activation of the GABP Beta promoter by an NRF-1-containing complex
title_fullStr Decreased expression of BRCA1 in SK-BR-3 cells is the result of aberrant activation of the GABP Beta promoter by an NRF-1-containing complex
title_full_unstemmed Decreased expression of BRCA1 in SK-BR-3 cells is the result of aberrant activation of the GABP Beta promoter by an NRF-1-containing complex
title_short Decreased expression of BRCA1 in SK-BR-3 cells is the result of aberrant activation of the GABP Beta promoter by an NRF-1-containing complex
title_sort decreased expression of brca1 in sk br 3 cells is the result of aberrant activation of the gabp beta promoter by an nrf 1 containing complex
url http://www.molecular-cancer.com/content/10/1/62
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AT thompsoncrista decreasedexpressionofbrca1inskbr3cellsistheresultofaberrantactivationofthegabpbetapromoterbyannrf1containingcomplex
AT muellerchristopherr decreasedexpressionofbrca1inskbr3cellsistheresultofaberrantactivationofthegabpbetapromoterbyannrf1containingcomplex