Mapping the chromatin landscape and Blimp1 transcriptional targets that regulate trophoblast differentiation
Abstract Trophoblast stem cells (TSCs) give rise to specialized cell types within the placenta. However, the regulatory mechanisms that guide trophoblast cell fate decisions during placenta development remain ill defined. Here we exploited ATAC-seq and transcriptional profiling strategies to describ...
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doaj-26d028b01be84c588d0195e0202b97a32020-12-08T01:18:52ZengNature Publishing GroupScientific Reports2045-23222017-07-017111510.1038/s41598-017-06859-9Mapping the chromatin landscape and Blimp1 transcriptional targets that regulate trophoblast differentiationAndrew C. Nelson0Arne W. Mould1Elizabeth K. Bikoff2Elizabeth J. Robertson3Sir William Dunn School of Pathology, University of OxfordSir William Dunn School of Pathology, University of OxfordSir William Dunn School of Pathology, University of OxfordSir William Dunn School of Pathology, University of OxfordAbstract Trophoblast stem cells (TSCs) give rise to specialized cell types within the placenta. However, the regulatory mechanisms that guide trophoblast cell fate decisions during placenta development remain ill defined. Here we exploited ATAC-seq and transcriptional profiling strategies to describe dynamic changes in gene expression and chromatin accessibility during TSC differentiation. We detect significantly increased chromatin accessibility at key genes upregulated as TSCs exit from the stem cell state. However, downregulated gene expression is not simply due to the loss of chromatin accessibility in proximal regions. Additionally, transcriptional targets recognized by the zinc finger transcriptional repressor Prdm1/Blimp1, an essential regulator of placenta development, were identified in ChIP-seq experiments. Comparisons with previously reported ChIP-seq datasets for primordial germ cell-like cells and E18.5 small intestine, combined with functional annotation analysis revealed that Blimp1 has broadly shared as well as cell type-specific functional activities unique to the trophoblast lineage. Importantly, Blimp1 not only silences TSC gene expression but also prevents aberrant activation of divergent developmental programmes. Overall the present study provides new insights into the chromatin landscape and Blimp1-dependent regulatory networks governing trophoblast gene expression.https://doi.org/10.1038/s41598-017-06859-9 |
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DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Andrew C. Nelson Arne W. Mould Elizabeth K. Bikoff Elizabeth J. Robertson |
spellingShingle |
Andrew C. Nelson Arne W. Mould Elizabeth K. Bikoff Elizabeth J. Robertson Mapping the chromatin landscape and Blimp1 transcriptional targets that regulate trophoblast differentiation Scientific Reports |
author_facet |
Andrew C. Nelson Arne W. Mould Elizabeth K. Bikoff Elizabeth J. Robertson |
author_sort |
Andrew C. Nelson |
title |
Mapping the chromatin landscape and Blimp1 transcriptional targets that regulate trophoblast differentiation |
title_short |
Mapping the chromatin landscape and Blimp1 transcriptional targets that regulate trophoblast differentiation |
title_full |
Mapping the chromatin landscape and Blimp1 transcriptional targets that regulate trophoblast differentiation |
title_fullStr |
Mapping the chromatin landscape and Blimp1 transcriptional targets that regulate trophoblast differentiation |
title_full_unstemmed |
Mapping the chromatin landscape and Blimp1 transcriptional targets that regulate trophoblast differentiation |
title_sort |
mapping the chromatin landscape and blimp1 transcriptional targets that regulate trophoblast differentiation |
publisher |
Nature Publishing Group |
series |
Scientific Reports |
issn |
2045-2322 |
publishDate |
2017-07-01 |
description |
Abstract Trophoblast stem cells (TSCs) give rise to specialized cell types within the placenta. However, the regulatory mechanisms that guide trophoblast cell fate decisions during placenta development remain ill defined. Here we exploited ATAC-seq and transcriptional profiling strategies to describe dynamic changes in gene expression and chromatin accessibility during TSC differentiation. We detect significantly increased chromatin accessibility at key genes upregulated as TSCs exit from the stem cell state. However, downregulated gene expression is not simply due to the loss of chromatin accessibility in proximal regions. Additionally, transcriptional targets recognized by the zinc finger transcriptional repressor Prdm1/Blimp1, an essential regulator of placenta development, were identified in ChIP-seq experiments. Comparisons with previously reported ChIP-seq datasets for primordial germ cell-like cells and E18.5 small intestine, combined with functional annotation analysis revealed that Blimp1 has broadly shared as well as cell type-specific functional activities unique to the trophoblast lineage. Importantly, Blimp1 not only silences TSC gene expression but also prevents aberrant activation of divergent developmental programmes. Overall the present study provides new insights into the chromatin landscape and Blimp1-dependent regulatory networks governing trophoblast gene expression. |
url |
https://doi.org/10.1038/s41598-017-06859-9 |
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