Forkhead box O1 (FOXO1) protein, but not p53, contributes to robust induction of p21 expression in fasted mice

Autores
Tinkum, Kelsey L.; White, Lynn S.; Marpegan, Luciano; Herzog, Erik; Piwnica Worms, David; Piwnica Worms, Helen
Año de publicación
2013
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Reporter mice that enable the activity of the endogenous p21 promoter to be dynamically monitored in real time in vivo and under a variety of experimental conditions revealed ubiquitous p21 expression in mouse organs including the brain. Low light bioluminescence microscopy was employed to localize p21 expression to specific regions of the brain. Interestingly, p21 expression was observed in the paraventricular, arcuate, and dorsomedial nuclei of the hypothalamus, regions that detect nutrient levels in the blood stream and signal metabolic actions throughout the body. These results suggested a link between p21 expression and metabolic regulation. We found that short-term food deprivation (fasting) potently induced p21 expression in tissues involved in metabolic regulation including liver, pancreas and hypothalamic nuclei. Conditional reporter mice were generated that enabled hepatocyte-specific expression of p21 to be monitored in vivo. Bioluminescence imaging demonstrated that fasting induced a 7-fold increase in p21 expression in livers of reporter mice and Western blotting demonstrated an increase in protein levels as well. The ability of fasting to induce p21 expression was found to be independent of p53 but dependent on FOXO1. Finally, occupancy of the endogenous p21 promoter by FOXO1 was observed in the livers of fasted but not fed mice. Thus, fasting promotes loading of FOXO1 onto the p21 promoter to induce p21 expression in hepatocytes.
Fil: Tinkum, Kelsey L.. BRIGHT Institute; Estados Unidos. Mallinckrodt Institute of Radiology; Estados Unidos
Fil: White, Lynn S.. Mallinckrodt Institute of Radiology; Estados Unidos. BRIGHT Institute; Estados Unidos
Fil: Marpegan, Luciano. University of Washington; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Herzog, Erik. University of Washington; Estados Unidos
Fil: Piwnica Worms, David. Mallinckrodt Institute of Radiology; Estados Unidos. BRIGHT Institute; Estados Unidos
Fil: Piwnica Worms, Helen. Mallinckrodt Institute of Radiology; Estados Unidos. BRIGHT Institute; Estados Unidos
Materia
Diet
Foxo
Bioluminescence
Hypothalamus
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:11336/88198

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network_name_str CONICET Digital (CONICET)
spelling Forkhead box O1 (FOXO1) protein, but not p53, contributes to robust induction of p21 expression in fasted miceTinkum, Kelsey L.White, Lynn S.Marpegan, LucianoHerzog, ErikPiwnica Worms, DavidPiwnica Worms, HelenDietFoxoBioluminescenceHypothalamushttps://purl.org/becyt/ford/1.6https://purl.org/becyt/ford/1Reporter mice that enable the activity of the endogenous p21 promoter to be dynamically monitored in real time in vivo and under a variety of experimental conditions revealed ubiquitous p21 expression in mouse organs including the brain. Low light bioluminescence microscopy was employed to localize p21 expression to specific regions of the brain. Interestingly, p21 expression was observed in the paraventricular, arcuate, and dorsomedial nuclei of the hypothalamus, regions that detect nutrient levels in the blood stream and signal metabolic actions throughout the body. These results suggested a link between p21 expression and metabolic regulation. We found that short-term food deprivation (fasting) potently induced p21 expression in tissues involved in metabolic regulation including liver, pancreas and hypothalamic nuclei. Conditional reporter mice were generated that enabled hepatocyte-specific expression of p21 to be monitored in vivo. Bioluminescence imaging demonstrated that fasting induced a 7-fold increase in p21 expression in livers of reporter mice and Western blotting demonstrated an increase in protein levels as well. The ability of fasting to induce p21 expression was found to be independent of p53 but dependent on FOXO1. Finally, occupancy of the endogenous p21 promoter by FOXO1 was observed in the livers of fasted but not fed mice. Thus, fasting promotes loading of FOXO1 onto the p21 promoter to induce p21 expression in hepatocytes.Fil: Tinkum, Kelsey L.. BRIGHT Institute; Estados Unidos. Mallinckrodt Institute of Radiology; Estados UnidosFil: White, Lynn S.. Mallinckrodt Institute of Radiology; Estados Unidos. BRIGHT Institute; Estados UnidosFil: Marpegan, Luciano. University of Washington; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Herzog, Erik. University of Washington; Estados UnidosFil: Piwnica Worms, David. Mallinckrodt Institute of Radiology; Estados Unidos. BRIGHT Institute; Estados UnidosFil: Piwnica Worms, Helen. Mallinckrodt Institute of Radiology; Estados Unidos. BRIGHT Institute; Estados UnidosAmerican Society for Biochemistry and Molecular Biology2013-09info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/88198Tinkum, Kelsey L.; White, Lynn S.; Marpegan, Luciano; Herzog, Erik; Piwnica Worms, David; et al.; Forkhead box O1 (FOXO1) protein, but not p53, contributes to robust induction of p21 expression in fasted mice; American Society for Biochemistry and Molecular Biology; Journal of Biological Chemistry (online); 288; 39; 9-2013; 27999-280080021-9258CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1074/jbc.M113.494328info:eu-repo/semantics/altIdentifier/url/http://www.jbc.org/content/288/39/27999info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-22T11:45:20Zoai:ri.conicet.gov.ar:11336/88198instacron: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 11:45:20.668CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Forkhead box O1 (FOXO1) protein, but not p53, contributes to robust induction of p21 expression in fasted mice
title Forkhead box O1 (FOXO1) protein, but not p53, contributes to robust induction of p21 expression in fasted mice
spellingShingle Forkhead box O1 (FOXO1) protein, but not p53, contributes to robust induction of p21 expression in fasted mice
Tinkum, Kelsey L.
Diet
Foxo
Bioluminescence
Hypothalamus
title_short Forkhead box O1 (FOXO1) protein, but not p53, contributes to robust induction of p21 expression in fasted mice
title_full Forkhead box O1 (FOXO1) protein, but not p53, contributes to robust induction of p21 expression in fasted mice
title_fullStr Forkhead box O1 (FOXO1) protein, but not p53, contributes to robust induction of p21 expression in fasted mice
title_full_unstemmed Forkhead box O1 (FOXO1) protein, but not p53, contributes to robust induction of p21 expression in fasted mice
title_sort Forkhead box O1 (FOXO1) protein, but not p53, contributes to robust induction of p21 expression in fasted mice
dc.creator.none.fl_str_mv Tinkum, Kelsey L.
White, Lynn S.
Marpegan, Luciano
Herzog, Erik
Piwnica Worms, David
Piwnica Worms, Helen
author Tinkum, Kelsey L.
author_facet Tinkum, Kelsey L.
White, Lynn S.
Marpegan, Luciano
Herzog, Erik
Piwnica Worms, David
Piwnica Worms, Helen
author_role author
author2 White, Lynn S.
Marpegan, Luciano
Herzog, Erik
Piwnica Worms, David
Piwnica Worms, Helen
author2_role author
author
author
author
author
dc.subject.none.fl_str_mv Diet
Foxo
Bioluminescence
Hypothalamus
topic Diet
Foxo
Bioluminescence
Hypothalamus
purl_subject.fl_str_mv https://purl.org/becyt/ford/1.6
https://purl.org/becyt/ford/1
dc.description.none.fl_txt_mv Reporter mice that enable the activity of the endogenous p21 promoter to be dynamically monitored in real time in vivo and under a variety of experimental conditions revealed ubiquitous p21 expression in mouse organs including the brain. Low light bioluminescence microscopy was employed to localize p21 expression to specific regions of the brain. Interestingly, p21 expression was observed in the paraventricular, arcuate, and dorsomedial nuclei of the hypothalamus, regions that detect nutrient levels in the blood stream and signal metabolic actions throughout the body. These results suggested a link between p21 expression and metabolic regulation. We found that short-term food deprivation (fasting) potently induced p21 expression in tissues involved in metabolic regulation including liver, pancreas and hypothalamic nuclei. Conditional reporter mice were generated that enabled hepatocyte-specific expression of p21 to be monitored in vivo. Bioluminescence imaging demonstrated that fasting induced a 7-fold increase in p21 expression in livers of reporter mice and Western blotting demonstrated an increase in protein levels as well. The ability of fasting to induce p21 expression was found to be independent of p53 but dependent on FOXO1. Finally, occupancy of the endogenous p21 promoter by FOXO1 was observed in the livers of fasted but not fed mice. Thus, fasting promotes loading of FOXO1 onto the p21 promoter to induce p21 expression in hepatocytes.
Fil: Tinkum, Kelsey L.. BRIGHT Institute; Estados Unidos. Mallinckrodt Institute of Radiology; Estados Unidos
Fil: White, Lynn S.. Mallinckrodt Institute of Radiology; Estados Unidos. BRIGHT Institute; Estados Unidos
Fil: Marpegan, Luciano. University of Washington; Estados Unidos. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Herzog, Erik. University of Washington; Estados Unidos
Fil: Piwnica Worms, David. Mallinckrodt Institute of Radiology; Estados Unidos. BRIGHT Institute; Estados Unidos
Fil: Piwnica Worms, Helen. Mallinckrodt Institute of Radiology; Estados Unidos. BRIGHT Institute; Estados Unidos
description Reporter mice that enable the activity of the endogenous p21 promoter to be dynamically monitored in real time in vivo and under a variety of experimental conditions revealed ubiquitous p21 expression in mouse organs including the brain. Low light bioluminescence microscopy was employed to localize p21 expression to specific regions of the brain. Interestingly, p21 expression was observed in the paraventricular, arcuate, and dorsomedial nuclei of the hypothalamus, regions that detect nutrient levels in the blood stream and signal metabolic actions throughout the body. These results suggested a link between p21 expression and metabolic regulation. We found that short-term food deprivation (fasting) potently induced p21 expression in tissues involved in metabolic regulation including liver, pancreas and hypothalamic nuclei. Conditional reporter mice were generated that enabled hepatocyte-specific expression of p21 to be monitored in vivo. Bioluminescence imaging demonstrated that fasting induced a 7-fold increase in p21 expression in livers of reporter mice and Western blotting demonstrated an increase in protein levels as well. The ability of fasting to induce p21 expression was found to be independent of p53 but dependent on FOXO1. Finally, occupancy of the endogenous p21 promoter by FOXO1 was observed in the livers of fasted but not fed mice. Thus, fasting promotes loading of FOXO1 onto the p21 promoter to induce p21 expression in hepatocytes.
publishDate 2013
dc.date.none.fl_str_mv 2013-09
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/11336/88198
Tinkum, Kelsey L.; White, Lynn S.; Marpegan, Luciano; Herzog, Erik; Piwnica Worms, David; et al.; Forkhead box O1 (FOXO1) protein, but not p53, contributes to robust induction of p21 expression in fasted mice; American Society for Biochemistry and Molecular Biology; Journal of Biological Chemistry (online); 288; 39; 9-2013; 27999-28008
0021-9258
CONICET Digital
CONICET
url http://hdl.handle.net/11336/88198
identifier_str_mv Tinkum, Kelsey L.; White, Lynn S.; Marpegan, Luciano; Herzog, Erik; Piwnica Worms, David; et al.; Forkhead box O1 (FOXO1) protein, but not p53, contributes to robust induction of p21 expression in fasted mice; American Society for Biochemistry and Molecular Biology; Journal of Biological Chemistry (online); 288; 39; 9-2013; 27999-28008
0021-9258
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/doi/10.1074/jbc.M113.494328
info:eu-repo/semantics/altIdentifier/url/http://www.jbc.org/content/288/39/27999
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 American Society for Biochemistry and Molecular Biology
publisher.none.fl_str_mv American Society for Biochemistry and Molecular Biology
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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