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Xist/Tsix expression dynamics during mouse peri-implantation development revealed by whole-mount 3D RNA-FISH
During peri-implantation development in mice, X chromosome inactivation (XCI) status changes dynamically. Here, we examined the expression of Xist and its antisense partner, Tsix, via whole-mount 3D RNA-FISH using strand-specific probes and evaluated XCI status. The results indicate that Xist expres...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403393/ https://www.ncbi.nlm.nih.gov/pubmed/30842444 http://dx.doi.org/10.1038/s41598-019-38807-0 |
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author | Shiura, Hirosuke Abe, Kuniya |
author_facet | Shiura, Hirosuke Abe, Kuniya |
author_sort | Shiura, Hirosuke |
collection | PubMed |
description | During peri-implantation development in mice, X chromosome inactivation (XCI) status changes dynamically. Here, we examined the expression of Xist and its antisense partner, Tsix, via whole-mount 3D RNA-FISH using strand-specific probes and evaluated XCI status. The results indicate that Xist expression disappears completely by embryonic day (E) 4.5 without Tsix activation in the ICM and that Xist re-expression occurs at E4.75 in some cells, suggesting that random XCI is already initiated in these cells. Intriguingly, epiblast cells exhibiting biallelic Xist expression were observed frequently (~15%) at E5.25 and E5.5. Immunostaining analysis of epigenetic modifications suggests that global change in epigenomic status occurs concomitantly with the transition from imprinted to random XCI. However, global upregulation of H3K27me3 modifications initiated earlier than other modifications, occurring specifically in ICM during progression of Xist erasure. Although both Xist expression and imprinted XCI are thought to be stable in the primitive endoderm/visceral endoderm and trophectoderm/extraembryonic ectoderm lineages, transient loss of Xist clouds was noted only in a subset of extraembryonic ectodermal cells, suggesting distinct features of Xist regulation among the three different embryonic tissue layers. These results will serve as a basis for future functional studies of XCI regulation in vivo. |
format | Online Article Text |
id | pubmed-6403393 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64033932019-03-11 Xist/Tsix expression dynamics during mouse peri-implantation development revealed by whole-mount 3D RNA-FISH Shiura, Hirosuke Abe, Kuniya Sci Rep Article During peri-implantation development in mice, X chromosome inactivation (XCI) status changes dynamically. Here, we examined the expression of Xist and its antisense partner, Tsix, via whole-mount 3D RNA-FISH using strand-specific probes and evaluated XCI status. The results indicate that Xist expression disappears completely by embryonic day (E) 4.5 without Tsix activation in the ICM and that Xist re-expression occurs at E4.75 in some cells, suggesting that random XCI is already initiated in these cells. Intriguingly, epiblast cells exhibiting biallelic Xist expression were observed frequently (~15%) at E5.25 and E5.5. Immunostaining analysis of epigenetic modifications suggests that global change in epigenomic status occurs concomitantly with the transition from imprinted to random XCI. However, global upregulation of H3K27me3 modifications initiated earlier than other modifications, occurring specifically in ICM during progression of Xist erasure. Although both Xist expression and imprinted XCI are thought to be stable in the primitive endoderm/visceral endoderm and trophectoderm/extraembryonic ectoderm lineages, transient loss of Xist clouds was noted only in a subset of extraembryonic ectodermal cells, suggesting distinct features of Xist regulation among the three different embryonic tissue layers. These results will serve as a basis for future functional studies of XCI regulation in vivo. Nature Publishing Group UK 2019-03-06 /pmc/articles/PMC6403393/ /pubmed/30842444 http://dx.doi.org/10.1038/s41598-019-38807-0 Text en © The Author(s) 2019 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/. |
spellingShingle | Article Shiura, Hirosuke Abe, Kuniya Xist/Tsix expression dynamics during mouse peri-implantation development revealed by whole-mount 3D RNA-FISH |
title | Xist/Tsix expression dynamics during mouse peri-implantation development revealed by whole-mount 3D RNA-FISH |
title_full | Xist/Tsix expression dynamics during mouse peri-implantation development revealed by whole-mount 3D RNA-FISH |
title_fullStr | Xist/Tsix expression dynamics during mouse peri-implantation development revealed by whole-mount 3D RNA-FISH |
title_full_unstemmed | Xist/Tsix expression dynamics during mouse peri-implantation development revealed by whole-mount 3D RNA-FISH |
title_short | Xist/Tsix expression dynamics during mouse peri-implantation development revealed by whole-mount 3D RNA-FISH |
title_sort | xist/tsix expression dynamics during mouse peri-implantation development revealed by whole-mount 3d rna-fish |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6403393/ https://www.ncbi.nlm.nih.gov/pubmed/30842444 http://dx.doi.org/10.1038/s41598-019-38807-0 |
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