Endogenous CCAAT/enhancer binding protein beta and p300 are both regulated by growth hormone to mediate transcriptional activation

Autores
Cui, Tracy Xiao; Piwien Pilipuk, Graciela; Huo, Jeffrey S.; Kaplani, Julianne; Kwok, Roland; Schwartz, Jessica
Año de publicación
2005
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
The regulation of c-fos transcription by GH involves multiple factors, including CCAAT/enhancer binding protein (C/EBP)beta. Knockdown of C/EBPbeta by RNA interference prevents stimulation of endogenous c-fos mRNA by GH, indicating a key role for C/EBPbeta in GH-stimulated c-fos transcription. GH rapidly increases the occupancy of both endogenous C/EBPbeta and p300 on the c-fos promoter in 3T3-F442A preadipocytes as indicated by chromatin immunoprecipitation. The transient occupancy of p300 on c-fos and the presence of p300 in the anti-C/EBPbeta immunoprecipitate coincide with the transient increase in c-fos transcription with GH, suggesting that a nuclear complex containing  both p300 and C/EBPbeta occupies the c-fos promoter in response to GH. Expression of p300 with C/EBPbeta markedly increases c-fos promoter activity when neither alone is effective, indicating that p300 coactivates C/EBPbeta- mediated c-fos promoter activation. Such coactivation can determine a baseline for c-fos activation by GH. Furthermore, the occupancy of phosphorylated murine C/EBPbeta (T188) on c-fos upon GH treatment is simultaneous with increased occupancy by p300, suggesting that phospho-C/EBPbeta recruits p300 in response to GH. Thus, endogenous C/EBP beta and p300 on c-fos are dynamically regulated by GH to determine transcriptional activation. Phosphorylated C/EBPbeta and p300 appear to function as part of a regulated complex that mediates GH-stimulated transcription.
Fil: Cui, Tracy Xiao. University of Michigan; Estados Unidos
Fil: Piwien Pilipuk, Graciela. University of Michigan; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Huo, Jeffrey S.. University of Michigan; Estados Unidos
Fil: Kaplani, Julianne. University of Michigan; Estados Unidos
Fil: Kwok, Roland. University of Michigan; Estados Unidos
Fil: Schwartz, Jessica. University of Michigan; Estados Unidos
Materia
C/Ebpbeta
P300
Gh
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/36082

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repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Endogenous CCAAT/enhancer binding protein beta and p300 are both regulated by growth hormone to mediate transcriptional activationCui, Tracy XiaoPiwien Pilipuk, GracielaHuo, Jeffrey S.Kaplani, JulianneKwok, RolandSchwartz, JessicaC/EbpbetaP300Ghhttps://purl.org/becyt/ford/3.1https://purl.org/becyt/ford/3The regulation of c-fos transcription by GH involves multiple factors, including CCAAT/enhancer binding protein (C/EBP)beta. Knockdown of C/EBPbeta by RNA interference prevents stimulation of endogenous c-fos mRNA by GH, indicating a key role for C/EBPbeta in GH-stimulated c-fos transcription. GH rapidly increases the occupancy of both endogenous C/EBPbeta and p300 on the c-fos promoter in 3T3-F442A preadipocytes as indicated by chromatin immunoprecipitation. The transient occupancy of p300 on c-fos and the presence of p300 in the anti-C/EBPbeta immunoprecipitate coincide with the transient increase in c-fos transcription with GH, suggesting that a nuclear complex containing  both p300 and C/EBPbeta occupies the c-fos promoter in response to GH. Expression of p300 with C/EBPbeta markedly increases c-fos promoter activity when neither alone is effective, indicating that p300 coactivates C/EBPbeta- mediated c-fos promoter activation. Such coactivation can determine a baseline for c-fos activation by GH. Furthermore, the occupancy of phosphorylated murine C/EBPbeta (T188) on c-fos upon GH treatment is simultaneous with increased occupancy by p300, suggesting that phospho-C/EBPbeta recruits p300 in response to GH. Thus, endogenous C/EBP beta and p300 on c-fos are dynamically regulated by GH to determine transcriptional activation. Phosphorylated C/EBPbeta and p300 appear to function as part of a regulated complex that mediates GH-stimulated transcription.Fil: Cui, Tracy Xiao. University of Michigan; Estados UnidosFil: Piwien Pilipuk, Graciela. University of Michigan; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Huo, Jeffrey S.. University of Michigan; Estados UnidosFil: Kaplani, Julianne. University of Michigan; Estados UnidosFil: Kwok, Roland. University of Michigan; Estados UnidosFil: Schwartz, Jessica. University of Michigan; Estados UnidosEndocrine Society2005-08info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/36082Cui, Tracy Xiao; Piwien Pilipuk, Graciela; Huo, Jeffrey S.; Kaplani, Julianne; Kwok, Roland; et al.; Endogenous CCAAT/enhancer binding protein beta and p300 are both regulated by growth hormone to mediate transcriptional activation; Endocrine Society; Molecular Endocrinology; 19; 8; 8-2005; 2175-21860888-8809CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/mend/article/19/8/2175/2738190info:eu-repo/semantics/altIdentifier/doi/10.1210/me.2004-0502info:eu-repo/semantics/altIdentifier/pmid/15860545info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T12:04:56Zoai:ri.conicet.gov.ar:11336/36082instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-22 12:04:56.699CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Endogenous CCAAT/enhancer binding protein beta and p300 are both regulated by growth hormone to mediate transcriptional activation
title Endogenous CCAAT/enhancer binding protein beta and p300 are both regulated by growth hormone to mediate transcriptional activation
spellingShingle Endogenous CCAAT/enhancer binding protein beta and p300 are both regulated by growth hormone to mediate transcriptional activation
Cui, Tracy Xiao
C/Ebpbeta
P300
Gh
title_short Endogenous CCAAT/enhancer binding protein beta and p300 are both regulated by growth hormone to mediate transcriptional activation
title_full Endogenous CCAAT/enhancer binding protein beta and p300 are both regulated by growth hormone to mediate transcriptional activation
title_fullStr Endogenous CCAAT/enhancer binding protein beta and p300 are both regulated by growth hormone to mediate transcriptional activation
title_full_unstemmed Endogenous CCAAT/enhancer binding protein beta and p300 are both regulated by growth hormone to mediate transcriptional activation
title_sort Endogenous CCAAT/enhancer binding protein beta and p300 are both regulated by growth hormone to mediate transcriptional activation
dc.creator.none.fl_str_mv Cui, Tracy Xiao
Piwien Pilipuk, Graciela
Huo, Jeffrey S.
Kaplani, Julianne
Kwok, Roland
Schwartz, Jessica
author Cui, Tracy Xiao
author_facet Cui, Tracy Xiao
Piwien Pilipuk, Graciela
Huo, Jeffrey S.
Kaplani, Julianne
Kwok, Roland
Schwartz, Jessica
author_role author
author2 Piwien Pilipuk, Graciela
Huo, Jeffrey S.
Kaplani, Julianne
Kwok, Roland
Schwartz, Jessica
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv C/Ebpbeta
P300
Gh
topic C/Ebpbeta
P300
Gh
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.1
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv The regulation of c-fos transcription by GH involves multiple factors, including CCAAT/enhancer binding protein (C/EBP)beta. Knockdown of C/EBPbeta by RNA interference prevents stimulation of endogenous c-fos mRNA by GH, indicating a key role for C/EBPbeta in GH-stimulated c-fos transcription. GH rapidly increases the occupancy of both endogenous C/EBPbeta and p300 on the c-fos promoter in 3T3-F442A preadipocytes as indicated by chromatin immunoprecipitation. The transient occupancy of p300 on c-fos and the presence of p300 in the anti-C/EBPbeta immunoprecipitate coincide with the transient increase in c-fos transcription with GH, suggesting that a nuclear complex containing  both p300 and C/EBPbeta occupies the c-fos promoter in response to GH. Expression of p300 with C/EBPbeta markedly increases c-fos promoter activity when neither alone is effective, indicating that p300 coactivates C/EBPbeta- mediated c-fos promoter activation. Such coactivation can determine a baseline for c-fos activation by GH. Furthermore, the occupancy of phosphorylated murine C/EBPbeta (T188) on c-fos upon GH treatment is simultaneous with increased occupancy by p300, suggesting that phospho-C/EBPbeta recruits p300 in response to GH. Thus, endogenous C/EBP beta and p300 on c-fos are dynamically regulated by GH to determine transcriptional activation. Phosphorylated C/EBPbeta and p300 appear to function as part of a regulated complex that mediates GH-stimulated transcription.
Fil: Cui, Tracy Xiao. University of Michigan; Estados Unidos
Fil: Piwien Pilipuk, Graciela. University of Michigan; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Huo, Jeffrey S.. University of Michigan; Estados Unidos
Fil: Kaplani, Julianne. University of Michigan; Estados Unidos
Fil: Kwok, Roland. University of Michigan; Estados Unidos
Fil: Schwartz, Jessica. University of Michigan; Estados Unidos
description The regulation of c-fos transcription by GH involves multiple factors, including CCAAT/enhancer binding protein (C/EBP)beta. Knockdown of C/EBPbeta by RNA interference prevents stimulation of endogenous c-fos mRNA by GH, indicating a key role for C/EBPbeta in GH-stimulated c-fos transcription. GH rapidly increases the occupancy of both endogenous C/EBPbeta and p300 on the c-fos promoter in 3T3-F442A preadipocytes as indicated by chromatin immunoprecipitation. The transient occupancy of p300 on c-fos and the presence of p300 in the anti-C/EBPbeta immunoprecipitate coincide with the transient increase in c-fos transcription with GH, suggesting that a nuclear complex containing  both p300 and C/EBPbeta occupies the c-fos promoter in response to GH. Expression of p300 with C/EBPbeta markedly increases c-fos promoter activity when neither alone is effective, indicating that p300 coactivates C/EBPbeta- mediated c-fos promoter activation. Such coactivation can determine a baseline for c-fos activation by GH. Furthermore, the occupancy of phosphorylated murine C/EBPbeta (T188) on c-fos upon GH treatment is simultaneous with increased occupancy by p300, suggesting that phospho-C/EBPbeta recruits p300 in response to GH. Thus, endogenous C/EBP beta and p300 on c-fos are dynamically regulated by GH to determine transcriptional activation. Phosphorylated C/EBPbeta and p300 appear to function as part of a regulated complex that mediates GH-stimulated transcription.
publishDate 2005
dc.date.none.fl_str_mv 2005-08
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/36082
Cui, Tracy Xiao; Piwien Pilipuk, Graciela; Huo, Jeffrey S.; Kaplani, Julianne; Kwok, Roland; et al.; Endogenous CCAAT/enhancer binding protein beta and p300 are both regulated by growth hormone to mediate transcriptional activation; Endocrine Society; Molecular Endocrinology; 19; 8; 8-2005; 2175-2186
0888-8809
CONICET Digital
CONICET
url http://hdl.handle.net/11336/36082
identifier_str_mv Cui, Tracy Xiao; Piwien Pilipuk, Graciela; Huo, Jeffrey S.; Kaplani, Julianne; Kwok, Roland; et al.; Endogenous CCAAT/enhancer binding protein beta and p300 are both regulated by growth hormone to mediate transcriptional activation; Endocrine Society; Molecular Endocrinology; 19; 8; 8-2005; 2175-2186
0888-8809
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://academic.oup.com/mend/article/19/8/2175/2738190
info:eu-repo/semantics/altIdentifier/doi/10.1210/me.2004-0502
info:eu-repo/semantics/altIdentifier/pmid/15860545
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Endocrine Society
publisher.none.fl_str_mv Endocrine Society
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
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