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Direct targets of Klf5 transcription factor contribute to the maintenance of mouse embryonic stem cell undifferentiated state

BACKGROUND: A growing body of evidence has shown that Krüppel-like transcription factors play a crucial role in maintaining embryonic stem cell (ESC) pluripotency and in governing ESC fate decisions. Krüppel-like factor 5 (Klf5) appears to play a critical role in these processes, but detailed knowle...

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Autores principales: Parisi, Silvia, Cozzuto, Luca, Tarantino, Carolina, Passaro, Fabiana, Ciriello, Simona, Aloia, Luigi, Antonini, Dario, De Simone, Vincenzo, Pastore, Lucio, Russo, Tommaso
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955566/
https://www.ncbi.nlm.nih.gov/pubmed/20875108
http://dx.doi.org/10.1186/1741-7007-8-128
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author Parisi, Silvia
Cozzuto, Luca
Tarantino, Carolina
Passaro, Fabiana
Ciriello, Simona
Aloia, Luigi
Antonini, Dario
De Simone, Vincenzo
Pastore, Lucio
Russo, Tommaso
author_facet Parisi, Silvia
Cozzuto, Luca
Tarantino, Carolina
Passaro, Fabiana
Ciriello, Simona
Aloia, Luigi
Antonini, Dario
De Simone, Vincenzo
Pastore, Lucio
Russo, Tommaso
author_sort Parisi, Silvia
collection PubMed
description BACKGROUND: A growing body of evidence has shown that Krüppel-like transcription factors play a crucial role in maintaining embryonic stem cell (ESC) pluripotency and in governing ESC fate decisions. Krüppel-like factor 5 (Klf5) appears to play a critical role in these processes, but detailed knowledge of the molecular mechanisms of this function is still not completely addressed. RESULTS: By combining genome-wide chromatin immunoprecipitation and microarray analysis, we have identified 161 putative primary targets of Klf5 in ESCs. We address three main points: (1) the relevance of the pathways governed by Klf5, demonstrating that suppression or constitutive expression of single Klf5 targets robustly affect the ESC undifferentiated phenotype; (2) the specificity of Klf5 compared to factors belonging to the same family, demonstrating that many Klf5 targets are not regulated by Klf2 and Klf4; and (3) the specificity of Klf5 function in ESCs, demonstrated by the significant differences between Klf5 targets in ESCs compared to adult cells, such as keratinocytes. CONCLUSIONS: Taken together, these results, through the definition of a detailed list of Klf5 transcriptional targets in mouse ESCs, support the important and specific functional role of Klf5 in the maintenance of the undifferentiated ESC phenotype. See: http://www.biomedcental.com/1741-7007/8/125
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spelling pubmed-29555662010-10-16 Direct targets of Klf5 transcription factor contribute to the maintenance of mouse embryonic stem cell undifferentiated state Parisi, Silvia Cozzuto, Luca Tarantino, Carolina Passaro, Fabiana Ciriello, Simona Aloia, Luigi Antonini, Dario De Simone, Vincenzo Pastore, Lucio Russo, Tommaso BMC Biol Research Article BACKGROUND: A growing body of evidence has shown that Krüppel-like transcription factors play a crucial role in maintaining embryonic stem cell (ESC) pluripotency and in governing ESC fate decisions. Krüppel-like factor 5 (Klf5) appears to play a critical role in these processes, but detailed knowledge of the molecular mechanisms of this function is still not completely addressed. RESULTS: By combining genome-wide chromatin immunoprecipitation and microarray analysis, we have identified 161 putative primary targets of Klf5 in ESCs. We address three main points: (1) the relevance of the pathways governed by Klf5, demonstrating that suppression or constitutive expression of single Klf5 targets robustly affect the ESC undifferentiated phenotype; (2) the specificity of Klf5 compared to factors belonging to the same family, demonstrating that many Klf5 targets are not regulated by Klf2 and Klf4; and (3) the specificity of Klf5 function in ESCs, demonstrated by the significant differences between Klf5 targets in ESCs compared to adult cells, such as keratinocytes. CONCLUSIONS: Taken together, these results, through the definition of a detailed list of Klf5 transcriptional targets in mouse ESCs, support the important and specific functional role of Klf5 in the maintenance of the undifferentiated ESC phenotype. See: http://www.biomedcental.com/1741-7007/8/125 BioMed Central 2010-09-27 /pmc/articles/PMC2955566/ /pubmed/20875108 http://dx.doi.org/10.1186/1741-7007-8-128 Text en Copyright ©2010 Parisi et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Parisi, Silvia
Cozzuto, Luca
Tarantino, Carolina
Passaro, Fabiana
Ciriello, Simona
Aloia, Luigi
Antonini, Dario
De Simone, Vincenzo
Pastore, Lucio
Russo, Tommaso
Direct targets of Klf5 transcription factor contribute to the maintenance of mouse embryonic stem cell undifferentiated state
title Direct targets of Klf5 transcription factor contribute to the maintenance of mouse embryonic stem cell undifferentiated state
title_full Direct targets of Klf5 transcription factor contribute to the maintenance of mouse embryonic stem cell undifferentiated state
title_fullStr Direct targets of Klf5 transcription factor contribute to the maintenance of mouse embryonic stem cell undifferentiated state
title_full_unstemmed Direct targets of Klf5 transcription factor contribute to the maintenance of mouse embryonic stem cell undifferentiated state
title_short Direct targets of Klf5 transcription factor contribute to the maintenance of mouse embryonic stem cell undifferentiated state
title_sort direct targets of klf5 transcription factor contribute to the maintenance of mouse embryonic stem cell undifferentiated state
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2955566/
https://www.ncbi.nlm.nih.gov/pubmed/20875108
http://dx.doi.org/10.1186/1741-7007-8-128
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