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The bipartite TAD organization of the X-inactivation center ensures opposing developmental regulation of Tsix and Xist

The mouse X-inactivation center (Xic) locus represents a powerful model for understanding the links between genome architecture and gene regulation, with the non-coding genes Xist and Tsix showing opposite developmental expression patterns while being organized as an overlapping sense/antisense unit...

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Autores principales: van Bemmel, Joke G., Galupa, Rafael, Gard, Chris, Servant, Nicolas, Picard, Christel, Davies, James, Szempruch, Anthony James, Zhan, Yinxiu, Żylicz, Jan J., Nora, Elphège P., Lameiras, Sonia, de Wit, Elzo, Gentien, David, Baulande, Sylvain, Giorgetti, Luca, Guttman, Mitchell, Hughes, Jim R., Higgs, Douglas R., Gribnau, Joost, Heard, Edith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551226/
https://www.ncbi.nlm.nih.gov/pubmed/31133748
http://dx.doi.org/10.1038/s41588-019-0412-0
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author van Bemmel, Joke G.
Galupa, Rafael
Gard, Chris
Servant, Nicolas
Picard, Christel
Davies, James
Szempruch, Anthony James
Zhan, Yinxiu
Żylicz, Jan J.
Nora, Elphège P.
Lameiras, Sonia
de Wit, Elzo
Gentien, David
Baulande, Sylvain
Giorgetti, Luca
Guttman, Mitchell
Hughes, Jim R.
Higgs, Douglas R.
Gribnau, Joost
Heard, Edith
author_facet van Bemmel, Joke G.
Galupa, Rafael
Gard, Chris
Servant, Nicolas
Picard, Christel
Davies, James
Szempruch, Anthony James
Zhan, Yinxiu
Żylicz, Jan J.
Nora, Elphège P.
Lameiras, Sonia
de Wit, Elzo
Gentien, David
Baulande, Sylvain
Giorgetti, Luca
Guttman, Mitchell
Hughes, Jim R.
Higgs, Douglas R.
Gribnau, Joost
Heard, Edith
author_sort van Bemmel, Joke G.
collection PubMed
description The mouse X-inactivation center (Xic) locus represents a powerful model for understanding the links between genome architecture and gene regulation, with the non-coding genes Xist and Tsix showing opposite developmental expression patterns while being organized as an overlapping sense/antisense unit. The Xic is organized into two topologically associating domains (TADs) but the role of this architecture in orchestrating cis-regulatory information remains elusive. To explore this, we generated genomic inversions that swap the Xist/Tsix transcriptional unit and place their promoters in each other’s TAD. We found that this led to a switch in their expression dynamics: Xist became precociously and ectopically up-regulated, both in male and female pluripotent cells, while Tsix expression aberrantly persisted during differentiation. The topological partitioning of the Xic is thus critical to ensure proper developmental timing of X inactivation. Our study illustrates how the genomic architecture of cis-regulatory landscapes can affect the regulation of mammalian developmental processes.
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spelling pubmed-65512262019-11-27 The bipartite TAD organization of the X-inactivation center ensures opposing developmental regulation of Tsix and Xist van Bemmel, Joke G. Galupa, Rafael Gard, Chris Servant, Nicolas Picard, Christel Davies, James Szempruch, Anthony James Zhan, Yinxiu Żylicz, Jan J. Nora, Elphège P. Lameiras, Sonia de Wit, Elzo Gentien, David Baulande, Sylvain Giorgetti, Luca Guttman, Mitchell Hughes, Jim R. Higgs, Douglas R. Gribnau, Joost Heard, Edith Nat Genet Article The mouse X-inactivation center (Xic) locus represents a powerful model for understanding the links between genome architecture and gene regulation, with the non-coding genes Xist and Tsix showing opposite developmental expression patterns while being organized as an overlapping sense/antisense unit. The Xic is organized into two topologically associating domains (TADs) but the role of this architecture in orchestrating cis-regulatory information remains elusive. To explore this, we generated genomic inversions that swap the Xist/Tsix transcriptional unit and place their promoters in each other’s TAD. We found that this led to a switch in their expression dynamics: Xist became precociously and ectopically up-regulated, both in male and female pluripotent cells, while Tsix expression aberrantly persisted during differentiation. The topological partitioning of the Xic is thus critical to ensure proper developmental timing of X inactivation. Our study illustrates how the genomic architecture of cis-regulatory landscapes can affect the regulation of mammalian developmental processes. 2019-05-27 2019-06 /pmc/articles/PMC6551226/ /pubmed/31133748 http://dx.doi.org/10.1038/s41588-019-0412-0 Text en Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
van Bemmel, Joke G.
Galupa, Rafael
Gard, Chris
Servant, Nicolas
Picard, Christel
Davies, James
Szempruch, Anthony James
Zhan, Yinxiu
Żylicz, Jan J.
Nora, Elphège P.
Lameiras, Sonia
de Wit, Elzo
Gentien, David
Baulande, Sylvain
Giorgetti, Luca
Guttman, Mitchell
Hughes, Jim R.
Higgs, Douglas R.
Gribnau, Joost
Heard, Edith
The bipartite TAD organization of the X-inactivation center ensures opposing developmental regulation of Tsix and Xist
title The bipartite TAD organization of the X-inactivation center ensures opposing developmental regulation of Tsix and Xist
title_full The bipartite TAD organization of the X-inactivation center ensures opposing developmental regulation of Tsix and Xist
title_fullStr The bipartite TAD organization of the X-inactivation center ensures opposing developmental regulation of Tsix and Xist
title_full_unstemmed The bipartite TAD organization of the X-inactivation center ensures opposing developmental regulation of Tsix and Xist
title_short The bipartite TAD organization of the X-inactivation center ensures opposing developmental regulation of Tsix and Xist
title_sort bipartite tad organization of the x-inactivation center ensures opposing developmental regulation of tsix and xist
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6551226/
https://www.ncbi.nlm.nih.gov/pubmed/31133748
http://dx.doi.org/10.1038/s41588-019-0412-0
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