Cargando…
Notch and Hippo signaling converge on Strawberry Notch 1 (Sbno1) to synergistically activate Cdx2 during specification of the trophectoderm
The first binary cell fate decision occurs at the morula stage and gives rise to two distinct types of cells that constitute the trophectoderm (TE) and inner cell mass (ICM). The cell fate determinant, Cdx2, is induced in TE cells and plays an essential role in their differentiation and maintenance....
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389439/ https://www.ncbi.nlm.nih.gov/pubmed/28401892 http://dx.doi.org/10.1038/srep46135 |
_version_ | 1782521274111623168 |
---|---|
author | Watanabe, Yusuke Miyasaka, Kota Y. Kubo, Atsushi Kida, Yasuyuki S. Nakagawa, Osamu Hirate, Yoshikazu Sasaki, Hiroshi Ogura, Toshihiko |
author_facet | Watanabe, Yusuke Miyasaka, Kota Y. Kubo, Atsushi Kida, Yasuyuki S. Nakagawa, Osamu Hirate, Yoshikazu Sasaki, Hiroshi Ogura, Toshihiko |
author_sort | Watanabe, Yusuke |
collection | PubMed |
description | The first binary cell fate decision occurs at the morula stage and gives rise to two distinct types of cells that constitute the trophectoderm (TE) and inner cell mass (ICM). The cell fate determinant, Cdx2, is induced in TE cells and plays an essential role in their differentiation and maintenance. Notch and Hippo signaling cascades are assumed to converge onto regulatory elements of Cdx2, however, the underlying molecular mechanisms are largely unknown. Here, we show involvement of Strawberry Notch1 (Sbno1), a novel chromatin factor of the helicase superfamily 2, during preimplantation development. Sbno1 knockout embryos die at the preimplantation stage without forming a blastocoel, and Cdx2 is not turned on even though both Yap and Tead4 reside normally in nuclei. Accordingly, Sbno1 acts on the trophectoderm-enhancer (TEE) of Cdx2, ensuring its robust and synergistic activation by the Yap/Tead4 and NICD/Rbpj complexes. Interestingly, this synergism is enhanced when cells are mechanically stretched, which might reflect that TE cells are continuously stretched by the expanding ICM and blastocoel cavity. In addition, the histone chaperone, FACT (FAcilitates Chromatin Transcription) physically interacts with Sbno1. Our data provide new evidence on TE specification, highlighting unexpected but essential functions of the highly conserved chromatin factor, Sbno1. |
format | Online Article Text |
id | pubmed-5389439 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53894392017-04-14 Notch and Hippo signaling converge on Strawberry Notch 1 (Sbno1) to synergistically activate Cdx2 during specification of the trophectoderm Watanabe, Yusuke Miyasaka, Kota Y. Kubo, Atsushi Kida, Yasuyuki S. Nakagawa, Osamu Hirate, Yoshikazu Sasaki, Hiroshi Ogura, Toshihiko Sci Rep Article The first binary cell fate decision occurs at the morula stage and gives rise to two distinct types of cells that constitute the trophectoderm (TE) and inner cell mass (ICM). The cell fate determinant, Cdx2, is induced in TE cells and plays an essential role in their differentiation and maintenance. Notch and Hippo signaling cascades are assumed to converge onto regulatory elements of Cdx2, however, the underlying molecular mechanisms are largely unknown. Here, we show involvement of Strawberry Notch1 (Sbno1), a novel chromatin factor of the helicase superfamily 2, during preimplantation development. Sbno1 knockout embryos die at the preimplantation stage without forming a blastocoel, and Cdx2 is not turned on even though both Yap and Tead4 reside normally in nuclei. Accordingly, Sbno1 acts on the trophectoderm-enhancer (TEE) of Cdx2, ensuring its robust and synergistic activation by the Yap/Tead4 and NICD/Rbpj complexes. Interestingly, this synergism is enhanced when cells are mechanically stretched, which might reflect that TE cells are continuously stretched by the expanding ICM and blastocoel cavity. In addition, the histone chaperone, FACT (FAcilitates Chromatin Transcription) physically interacts with Sbno1. Our data provide new evidence on TE specification, highlighting unexpected but essential functions of the highly conserved chromatin factor, Sbno1. Nature Publishing Group 2017-04-12 /pmc/articles/PMC5389439/ /pubmed/28401892 http://dx.doi.org/10.1038/srep46135 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Watanabe, Yusuke Miyasaka, Kota Y. Kubo, Atsushi Kida, Yasuyuki S. Nakagawa, Osamu Hirate, Yoshikazu Sasaki, Hiroshi Ogura, Toshihiko Notch and Hippo signaling converge on Strawberry Notch 1 (Sbno1) to synergistically activate Cdx2 during specification of the trophectoderm |
title | Notch and Hippo signaling converge on Strawberry Notch 1 (Sbno1) to synergistically activate Cdx2 during specification of the trophectoderm |
title_full | Notch and Hippo signaling converge on Strawberry Notch 1 (Sbno1) to synergistically activate Cdx2 during specification of the trophectoderm |
title_fullStr | Notch and Hippo signaling converge on Strawberry Notch 1 (Sbno1) to synergistically activate Cdx2 during specification of the trophectoderm |
title_full_unstemmed | Notch and Hippo signaling converge on Strawberry Notch 1 (Sbno1) to synergistically activate Cdx2 during specification of the trophectoderm |
title_short | Notch and Hippo signaling converge on Strawberry Notch 1 (Sbno1) to synergistically activate Cdx2 during specification of the trophectoderm |
title_sort | notch and hippo signaling converge on strawberry notch 1 (sbno1) to synergistically activate cdx2 during specification of the trophectoderm |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5389439/ https://www.ncbi.nlm.nih.gov/pubmed/28401892 http://dx.doi.org/10.1038/srep46135 |
work_keys_str_mv | AT watanabeyusuke notchandhipposignalingconvergeonstrawberrynotch1sbno1tosynergisticallyactivatecdx2duringspecificationofthetrophectoderm AT miyasakakotay notchandhipposignalingconvergeonstrawberrynotch1sbno1tosynergisticallyactivatecdx2duringspecificationofthetrophectoderm AT kuboatsushi notchandhipposignalingconvergeonstrawberrynotch1sbno1tosynergisticallyactivatecdx2duringspecificationofthetrophectoderm AT kidayasuyukis notchandhipposignalingconvergeonstrawberrynotch1sbno1tosynergisticallyactivatecdx2duringspecificationofthetrophectoderm AT nakagawaosamu notchandhipposignalingconvergeonstrawberrynotch1sbno1tosynergisticallyactivatecdx2duringspecificationofthetrophectoderm AT hirateyoshikazu notchandhipposignalingconvergeonstrawberrynotch1sbno1tosynergisticallyactivatecdx2duringspecificationofthetrophectoderm AT sasakihiroshi notchandhipposignalingconvergeonstrawberrynotch1sbno1tosynergisticallyactivatecdx2duringspecificationofthetrophectoderm AT oguratoshihiko notchandhipposignalingconvergeonstrawberrynotch1sbno1tosynergisticallyactivatecdx2duringspecificationofthetrophectoderm |