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Regulatory landscape fusion in rhabdomyosarcoma through interactions between the PAX3 promoter and FOXO1 regulatory elements

BACKGROUND: The organisation of vertebrate genomes into topologically associating domains (TADs) is believed to facilitate the regulation of the genes located within them. A remaining question is whether TAD organisation is achieved through the interactions of the regulatory elements within them or...

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Autores principales: Vicente-García, Cristina, Villarejo-Balcells, Barbara, Irastorza-Azcárate, Ibai, Naranjo, Silvia, Acemel, Rafael D., Tena, Juan J., Rigby, Peter W. J., Devos, Damien P., Gómez-Skarmeta, Jose L., Carvajal, Jaime J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470208/
https://www.ncbi.nlm.nih.gov/pubmed/28615069
http://dx.doi.org/10.1186/s13059-017-1225-z
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author Vicente-García, Cristina
Villarejo-Balcells, Barbara
Irastorza-Azcárate, Ibai
Naranjo, Silvia
Acemel, Rafael D.
Tena, Juan J.
Rigby, Peter W. J.
Devos, Damien P.
Gómez-Skarmeta, Jose L.
Carvajal, Jaime J.
author_facet Vicente-García, Cristina
Villarejo-Balcells, Barbara
Irastorza-Azcárate, Ibai
Naranjo, Silvia
Acemel, Rafael D.
Tena, Juan J.
Rigby, Peter W. J.
Devos, Damien P.
Gómez-Skarmeta, Jose L.
Carvajal, Jaime J.
author_sort Vicente-García, Cristina
collection PubMed
description BACKGROUND: The organisation of vertebrate genomes into topologically associating domains (TADs) is believed to facilitate the regulation of the genes located within them. A remaining question is whether TAD organisation is achieved through the interactions of the regulatory elements within them or if these interactions are favoured by the pre-existence of TADs. If the latter is true, the fusion of two independent TADs should result in the rewiring of the transcriptional landscape and the generation of ectopic contacts. RESULTS: We show that interactions within the PAX3 and FOXO1 domains are restricted to their respective TADs in normal conditions, while in a patient-derived alveolar rhabdomyosarcoma cell line, harbouring the diagnostic t(2;13)(q35;q14) translocation that brings together the PAX3 and FOXO1 genes, the PAX3 promoter interacts ectopically with FOXO1 sequences. Using a combination of 4C-seq datasets, we have modelled the three-dimensional organisation of the fused landscape in alveolar rhabdomyosarcoma. CONCLUSIONS: The chromosomal translocation that leads to alveolar rhabdomyosarcoma development generates a novel TAD that is likely to favour ectopic PAX3:FOXO1 oncogene activation in non-PAX3 territories. Rhabdomyosarcomas may therefore arise from cells which do not normally express PAX3. The borders of this novel TAD correspond to the original 5'- and 3'- borders of the PAX3 and FOXO1 TADs, respectively, suggesting that TAD organisation precedes the formation of regulatory long-range interactions. Our results demonstrate that, upon translocation, novel regulatory landscapes are formed allowing new intra-TAD interactions between the original loci involved. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-017-1225-z) contains supplementary material, which is available to authorized users.
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spelling pubmed-54702082017-06-19 Regulatory landscape fusion in rhabdomyosarcoma through interactions between the PAX3 promoter and FOXO1 regulatory elements Vicente-García, Cristina Villarejo-Balcells, Barbara Irastorza-Azcárate, Ibai Naranjo, Silvia Acemel, Rafael D. Tena, Juan J. Rigby, Peter W. J. Devos, Damien P. Gómez-Skarmeta, Jose L. Carvajal, Jaime J. Genome Biol Research BACKGROUND: The organisation of vertebrate genomes into topologically associating domains (TADs) is believed to facilitate the regulation of the genes located within them. A remaining question is whether TAD organisation is achieved through the interactions of the regulatory elements within them or if these interactions are favoured by the pre-existence of TADs. If the latter is true, the fusion of two independent TADs should result in the rewiring of the transcriptional landscape and the generation of ectopic contacts. RESULTS: We show that interactions within the PAX3 and FOXO1 domains are restricted to their respective TADs in normal conditions, while in a patient-derived alveolar rhabdomyosarcoma cell line, harbouring the diagnostic t(2;13)(q35;q14) translocation that brings together the PAX3 and FOXO1 genes, the PAX3 promoter interacts ectopically with FOXO1 sequences. Using a combination of 4C-seq datasets, we have modelled the three-dimensional organisation of the fused landscape in alveolar rhabdomyosarcoma. CONCLUSIONS: The chromosomal translocation that leads to alveolar rhabdomyosarcoma development generates a novel TAD that is likely to favour ectopic PAX3:FOXO1 oncogene activation in non-PAX3 territories. Rhabdomyosarcomas may therefore arise from cells which do not normally express PAX3. The borders of this novel TAD correspond to the original 5'- and 3'- borders of the PAX3 and FOXO1 TADs, respectively, suggesting that TAD organisation precedes the formation of regulatory long-range interactions. Our results demonstrate that, upon translocation, novel regulatory landscapes are formed allowing new intra-TAD interactions between the original loci involved. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-017-1225-z) contains supplementary material, which is available to authorized users. BioMed Central 2017-06-14 /pmc/articles/PMC5470208/ /pubmed/28615069 http://dx.doi.org/10.1186/s13059-017-1225-z Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Vicente-García, Cristina
Villarejo-Balcells, Barbara
Irastorza-Azcárate, Ibai
Naranjo, Silvia
Acemel, Rafael D.
Tena, Juan J.
Rigby, Peter W. J.
Devos, Damien P.
Gómez-Skarmeta, Jose L.
Carvajal, Jaime J.
Regulatory landscape fusion in rhabdomyosarcoma through interactions between the PAX3 promoter and FOXO1 regulatory elements
title Regulatory landscape fusion in rhabdomyosarcoma through interactions between the PAX3 promoter and FOXO1 regulatory elements
title_full Regulatory landscape fusion in rhabdomyosarcoma through interactions between the PAX3 promoter and FOXO1 regulatory elements
title_fullStr Regulatory landscape fusion in rhabdomyosarcoma through interactions between the PAX3 promoter and FOXO1 regulatory elements
title_full_unstemmed Regulatory landscape fusion in rhabdomyosarcoma through interactions between the PAX3 promoter and FOXO1 regulatory elements
title_short Regulatory landscape fusion in rhabdomyosarcoma through interactions between the PAX3 promoter and FOXO1 regulatory elements
title_sort regulatory landscape fusion in rhabdomyosarcoma through interactions between the pax3 promoter and foxo1 regulatory elements
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5470208/
https://www.ncbi.nlm.nih.gov/pubmed/28615069
http://dx.doi.org/10.1186/s13059-017-1225-z
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