Transcription Factor Antagonism Controls Enteroendocrine Cell Specification from Intestinal Stem Cells
Abstract The balanced maintenance and differentiation of local stem cells is required for Homeostatic renewal of tissues. In the Drosophila midgut, the transcription factor Escargot (Esg) maintains undifferentiated states in intestinal stem cells, whereas the transcription factors Scute (Sc) and Pro...
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2017-04-01
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Online Access: | https://doi.org/10.1038/s41598-017-01138-z |
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doaj-0d50718730f44815a12f3e844a13d3602020-12-08T01:40:45ZengNature Publishing GroupScientific Reports2045-23222017-04-017111210.1038/s41598-017-01138-zTranscription Factor Antagonism Controls Enteroendocrine Cell Specification from Intestinal Stem CellsYumei Li0Zhimin Pang1Huanwei Huang2Chenhui Wang3Tao Cai4Rongwen Xi5School of Life Science, Tsinghua UniversityNational Institute of Biological Sciences, Zhongguancun Life Science Park 7 Science Park RoadNational Institute of Biological Sciences, Zhongguancun Life Science Park 7 Science Park RoadNational Institute of Biological Sciences, Zhongguancun Life Science Park 7 Science Park RoadNational Institute of Biological Sciences, Zhongguancun Life Science Park 7 Science Park RoadNational Institute of Biological Sciences, Zhongguancun Life Science Park 7 Science Park RoadAbstract The balanced maintenance and differentiation of local stem cells is required for Homeostatic renewal of tissues. In the Drosophila midgut, the transcription factor Escargot (Esg) maintains undifferentiated states in intestinal stem cells, whereas the transcription factors Scute (Sc) and Prospero (Pros) promote enteroendocrine cell specification. However, the mechanism through which Esg and Sc/Pros coordinately regulate stem cell differentiation is unknown. Here, by combining chromatin immunoprecipitation analysis with genetic studies, we show that both Esg and Sc bind to a common promoter region of pros. Moreover, antagonistic activity between Esg and Sc controls the expression status of Pros in stem cells, thereby, specifying whether stem cells remain undifferentiated or commit to enteroendocrine cell differentiation. Our study therefore reveals transcription factor antagonism between Esg and Sc as a novel mechanism that underlies fate specification from intestinal stem cells in Drosophila.https://doi.org/10.1038/s41598-017-01138-z |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yumei Li Zhimin Pang Huanwei Huang Chenhui Wang Tao Cai Rongwen Xi |
spellingShingle |
Yumei Li Zhimin Pang Huanwei Huang Chenhui Wang Tao Cai Rongwen Xi Transcription Factor Antagonism Controls Enteroendocrine Cell Specification from Intestinal Stem Cells Scientific Reports |
author_facet |
Yumei Li Zhimin Pang Huanwei Huang Chenhui Wang Tao Cai Rongwen Xi |
author_sort |
Yumei Li |
title |
Transcription Factor Antagonism Controls Enteroendocrine Cell Specification from Intestinal Stem Cells |
title_short |
Transcription Factor Antagonism Controls Enteroendocrine Cell Specification from Intestinal Stem Cells |
title_full |
Transcription Factor Antagonism Controls Enteroendocrine Cell Specification from Intestinal Stem Cells |
title_fullStr |
Transcription Factor Antagonism Controls Enteroendocrine Cell Specification from Intestinal Stem Cells |
title_full_unstemmed |
Transcription Factor Antagonism Controls Enteroendocrine Cell Specification from Intestinal Stem Cells |
title_sort |
transcription factor antagonism controls enteroendocrine cell specification from intestinal stem cells |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2017-04-01 |
description |
Abstract The balanced maintenance and differentiation of local stem cells is required for Homeostatic renewal of tissues. In the Drosophila midgut, the transcription factor Escargot (Esg) maintains undifferentiated states in intestinal stem cells, whereas the transcription factors Scute (Sc) and Prospero (Pros) promote enteroendocrine cell specification. However, the mechanism through which Esg and Sc/Pros coordinately regulate stem cell differentiation is unknown. Here, by combining chromatin immunoprecipitation analysis with genetic studies, we show that both Esg and Sc bind to a common promoter region of pros. Moreover, antagonistic activity between Esg and Sc controls the expression status of Pros in stem cells, thereby, specifying whether stem cells remain undifferentiated or commit to enteroendocrine cell differentiation. Our study therefore reveals transcription factor antagonism between Esg and Sc as a novel mechanism that underlies fate specification from intestinal stem cells in Drosophila. |
url |
https://doi.org/10.1038/s41598-017-01138-z |
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