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Inversion of a topological domain leads to restricted changes in its gene expression and affects interdomain communication

The interplay between the topological organization of the genome and the regulation of gene expression remains unclear. Depletion of molecular factors (e.g. CTCF) underlying topologically associating domains (TADs) leads to modest alterations in gene expression, whereas genomic rearrangements involv...

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Autores principales: Galupa, Rafael, Picard, Christel, Servant, Nicolas, Nora, Elphège P., Zhan, Yinxiu, van Bemmel, Joke G., El Marjou, Fatima, Johanneau, Colin, Borensztein, Maud, Ancelin, Katia, Giorgetti, Luca, Heard, Edith
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Company of Biologists Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9148567/
https://www.ncbi.nlm.nih.gov/pubmed/35502750
http://dx.doi.org/10.1242/dev.200568
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author Galupa, Rafael
Picard, Christel
Servant, Nicolas
Nora, Elphège P.
Zhan, Yinxiu
van Bemmel, Joke G.
El Marjou, Fatima
Johanneau, Colin
Borensztein, Maud
Ancelin, Katia
Giorgetti, Luca
Heard, Edith
author_facet Galupa, Rafael
Picard, Christel
Servant, Nicolas
Nora, Elphège P.
Zhan, Yinxiu
van Bemmel, Joke G.
El Marjou, Fatima
Johanneau, Colin
Borensztein, Maud
Ancelin, Katia
Giorgetti, Luca
Heard, Edith
author_sort Galupa, Rafael
collection PubMed
description The interplay between the topological organization of the genome and the regulation of gene expression remains unclear. Depletion of molecular factors (e.g. CTCF) underlying topologically associating domains (TADs) leads to modest alterations in gene expression, whereas genomic rearrangements involving TAD boundaries disrupt normal gene expression and can lead to pathological phenotypes. Here, we targeted the TAD neighboring that of the noncoding transcript Xist, which controls X-chromosome inactivation. Inverting 245 kb within the TAD led to expected rearrangement of CTCF-based contacts but revealed heterogeneity in the ‘contact’ potential of different CTCF sites. Expression of most genes therein remained unaffected in mouse embryonic stem cells and during differentiation. Interestingly, expression of Xist was ectopically upregulated. The same inversion in mouse embryos led to biased Xist expression. Smaller inversions and deletions of CTCF clusters led to similar results: rearrangement of contacts and limited changes in local gene expression, but significant changes in Xist expression in embryos. Our study suggests that the wiring of regulatory interactions within a TAD can influence the expression of genes in neighboring TADs, highlighting the existence of mechanisms of inter-TAD communication.
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spelling pubmed-91485672022-07-01 Inversion of a topological domain leads to restricted changes in its gene expression and affects interdomain communication Galupa, Rafael Picard, Christel Servant, Nicolas Nora, Elphège P. Zhan, Yinxiu van Bemmel, Joke G. El Marjou, Fatima Johanneau, Colin Borensztein, Maud Ancelin, Katia Giorgetti, Luca Heard, Edith Development Research Article The interplay between the topological organization of the genome and the regulation of gene expression remains unclear. Depletion of molecular factors (e.g. CTCF) underlying topologically associating domains (TADs) leads to modest alterations in gene expression, whereas genomic rearrangements involving TAD boundaries disrupt normal gene expression and can lead to pathological phenotypes. Here, we targeted the TAD neighboring that of the noncoding transcript Xist, which controls X-chromosome inactivation. Inverting 245 kb within the TAD led to expected rearrangement of CTCF-based contacts but revealed heterogeneity in the ‘contact’ potential of different CTCF sites. Expression of most genes therein remained unaffected in mouse embryonic stem cells and during differentiation. Interestingly, expression of Xist was ectopically upregulated. The same inversion in mouse embryos led to biased Xist expression. Smaller inversions and deletions of CTCF clusters led to similar results: rearrangement of contacts and limited changes in local gene expression, but significant changes in Xist expression in embryos. Our study suggests that the wiring of regulatory interactions within a TAD can influence the expression of genes in neighboring TADs, highlighting the existence of mechanisms of inter-TAD communication. The Company of Biologists Ltd 2022-05-06 /pmc/articles/PMC9148567/ /pubmed/35502750 http://dx.doi.org/10.1242/dev.200568 Text en © 2022. Published by The Company of Biologists Ltd https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.
spellingShingle Research Article
Galupa, Rafael
Picard, Christel
Servant, Nicolas
Nora, Elphège P.
Zhan, Yinxiu
van Bemmel, Joke G.
El Marjou, Fatima
Johanneau, Colin
Borensztein, Maud
Ancelin, Katia
Giorgetti, Luca
Heard, Edith
Inversion of a topological domain leads to restricted changes in its gene expression and affects interdomain communication
title Inversion of a topological domain leads to restricted changes in its gene expression and affects interdomain communication
title_full Inversion of a topological domain leads to restricted changes in its gene expression and affects interdomain communication
title_fullStr Inversion of a topological domain leads to restricted changes in its gene expression and affects interdomain communication
title_full_unstemmed Inversion of a topological domain leads to restricted changes in its gene expression and affects interdomain communication
title_short Inversion of a topological domain leads to restricted changes in its gene expression and affects interdomain communication
title_sort inversion of a topological domain leads to restricted changes in its gene expression and affects interdomain communication
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9148567/
https://www.ncbi.nlm.nih.gov/pubmed/35502750
http://dx.doi.org/10.1242/dev.200568
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