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Menin directs regionalized decidual transformation through epigenetically setting PTX3 to balance FGF and BMP signaling

During decidualization in rodents, uterine stroma undergoes extensive reprograming into distinct cells, forming the discrete regions defined as the primary decidual zone (PDZ), the secondary decidual zone (SDZ) and the layer of undifferentiated stromal cells respectively. Here we show that uterine d...

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Autores principales: Liu, Mengying, Deng, Wenbo, Tang, Lu, Liu, Meng, Bao, Haili, Guo, Chuanhui, Zhang, Changxian, Lu, Jinhua, Wang, Haibin, Lu, Zhongxian, Kong, Shuangbo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8864016/
https://www.ncbi.nlm.nih.gov/pubmed/35194044
http://dx.doi.org/10.1038/s41467-022-28657-2
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author Liu, Mengying
Deng, Wenbo
Tang, Lu
Liu, Meng
Bao, Haili
Guo, Chuanhui
Zhang, Changxian
Lu, Jinhua
Wang, Haibin
Lu, Zhongxian
Kong, Shuangbo
author_facet Liu, Mengying
Deng, Wenbo
Tang, Lu
Liu, Meng
Bao, Haili
Guo, Chuanhui
Zhang, Changxian
Lu, Jinhua
Wang, Haibin
Lu, Zhongxian
Kong, Shuangbo
author_sort Liu, Mengying
collection PubMed
description During decidualization in rodents, uterine stroma undergoes extensive reprograming into distinct cells, forming the discrete regions defined as the primary decidual zone (PDZ), the secondary decidual zone (SDZ) and the layer of undifferentiated stromal cells respectively. Here we show that uterine deletion of Men1, a member of the histone H3K4 methyltransferase complex, disrupts the terminal differentiation of stroma, resulting in chaotic decidualization and pregnancy failure. Genome-wide epigenetic profile reveals that Men1 binding in chromatin recapitulates H3K4me3 distribution. Further transcriptomic investigation demonstrates that Men1 directly regulates the expression of PTX3, an extra-cellular trap for FGF2 in decidual cells. Decreased Ptx3 upon Men1 ablation leads to aberrant activation of ERK1/2 in the SDZ due to the unrestrained FGF2 signal emanated from undifferentiated stromal cells, which blunt BMP2 induction and decidualization. In brief, our study provides genetic and molecular mechanisms for epigenetic rewiring mediated decidual regionalization by Men1 and sheds new light on pregnancy maintenance.
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spelling pubmed-88640162022-03-17 Menin directs regionalized decidual transformation through epigenetically setting PTX3 to balance FGF and BMP signaling Liu, Mengying Deng, Wenbo Tang, Lu Liu, Meng Bao, Haili Guo, Chuanhui Zhang, Changxian Lu, Jinhua Wang, Haibin Lu, Zhongxian Kong, Shuangbo Nat Commun Article During decidualization in rodents, uterine stroma undergoes extensive reprograming into distinct cells, forming the discrete regions defined as the primary decidual zone (PDZ), the secondary decidual zone (SDZ) and the layer of undifferentiated stromal cells respectively. Here we show that uterine deletion of Men1, a member of the histone H3K4 methyltransferase complex, disrupts the terminal differentiation of stroma, resulting in chaotic decidualization and pregnancy failure. Genome-wide epigenetic profile reveals that Men1 binding in chromatin recapitulates H3K4me3 distribution. Further transcriptomic investigation demonstrates that Men1 directly regulates the expression of PTX3, an extra-cellular trap for FGF2 in decidual cells. Decreased Ptx3 upon Men1 ablation leads to aberrant activation of ERK1/2 in the SDZ due to the unrestrained FGF2 signal emanated from undifferentiated stromal cells, which blunt BMP2 induction and decidualization. In brief, our study provides genetic and molecular mechanisms for epigenetic rewiring mediated decidual regionalization by Men1 and sheds new light on pregnancy maintenance. Nature Publishing Group UK 2022-02-22 /pmc/articles/PMC8864016/ /pubmed/35194044 http://dx.doi.org/10.1038/s41467-022-28657-2 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Liu, Mengying
Deng, Wenbo
Tang, Lu
Liu, Meng
Bao, Haili
Guo, Chuanhui
Zhang, Changxian
Lu, Jinhua
Wang, Haibin
Lu, Zhongxian
Kong, Shuangbo
Menin directs regionalized decidual transformation through epigenetically setting PTX3 to balance FGF and BMP signaling
title Menin directs regionalized decidual transformation through epigenetically setting PTX3 to balance FGF and BMP signaling
title_full Menin directs regionalized decidual transformation through epigenetically setting PTX3 to balance FGF and BMP signaling
title_fullStr Menin directs regionalized decidual transformation through epigenetically setting PTX3 to balance FGF and BMP signaling
title_full_unstemmed Menin directs regionalized decidual transformation through epigenetically setting PTX3 to balance FGF and BMP signaling
title_short Menin directs regionalized decidual transformation through epigenetically setting PTX3 to balance FGF and BMP signaling
title_sort menin directs regionalized decidual transformation through epigenetically setting ptx3 to balance fgf and bmp signaling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8864016/
https://www.ncbi.nlm.nih.gov/pubmed/35194044
http://dx.doi.org/10.1038/s41467-022-28657-2
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