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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...
Autores principales: | , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2010
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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 |
format | Text |
id | pubmed-2955566 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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