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Miswired Enhancer Logic Drives a Cancer of the Muscle Lineage

Core regulatory transcription factors (CR TFs) establish enhancers with logical ordering during embryogenesis and development. Here we report that in fusion-positive rhabdomyosarcoma, a cancer of the muscle lineage, the chief oncogene PAX3-FOXO1 is driven by a translocated FOXO1 super enhancer (SE)...

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Autores principales: Gryder, Berkley E., Wachtel, Marco, Chang, Kenneth, El Demerdash, Osama, Aboreden, Nicholas G., Mohammed, Wardah, Ewert, Winston, Pomella, Silvia, Rota, Rossella, Wei, Jun S., Song, Young, Stanton, Benjamin Z., Schäfer, Beat, Vakoc, Christopher R., Khan, Javed
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226896/
https://www.ncbi.nlm.nih.gov/pubmed/32416589
http://dx.doi.org/10.1016/j.isci.2020.101103
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author Gryder, Berkley E.
Wachtel, Marco
Chang, Kenneth
El Demerdash, Osama
Aboreden, Nicholas G.
Mohammed, Wardah
Ewert, Winston
Pomella, Silvia
Rota, Rossella
Wei, Jun S.
Song, Young
Stanton, Benjamin Z.
Schäfer, Beat
Vakoc, Christopher R.
Khan, Javed
author_facet Gryder, Berkley E.
Wachtel, Marco
Chang, Kenneth
El Demerdash, Osama
Aboreden, Nicholas G.
Mohammed, Wardah
Ewert, Winston
Pomella, Silvia
Rota, Rossella
Wei, Jun S.
Song, Young
Stanton, Benjamin Z.
Schäfer, Beat
Vakoc, Christopher R.
Khan, Javed
author_sort Gryder, Berkley E.
collection PubMed
description Core regulatory transcription factors (CR TFs) establish enhancers with logical ordering during embryogenesis and development. Here we report that in fusion-positive rhabdomyosarcoma, a cancer of the muscle lineage, the chief oncogene PAX3-FOXO1 is driven by a translocated FOXO1 super enhancer (SE) restricted to a late stage of myogenesis. Using chromatin conformation capture techniques, we demonstrate that the extensive FOXO1 cis-regulatory domain interacts with PAX3. Furthermore, RNA sequencing and chromatin immunoprecipitation sequencing data in tumors bearing rare PAX translocations implicate enhancer miswiring across all fusion-positive tumors. HiChIP of H3K27ac showed connectivity between the FOXO1 SE, additional intra-domain enhancers, and the PAX3 promoter. We show that PAX3-FOXO1 transcription is diminished when this network of enhancers is ablated by CRISPR. Our data reveal a hijacked enhancer network that disrupts the stepwise CR TF logic of normal skeletal muscle development (PAX3 to MYOD to MYOG), replacing it with an “infinite loop” enhancer logic that locks rhabdomyosarcoma in an undifferentiated stage.
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spelling pubmed-72268962020-05-18 Miswired Enhancer Logic Drives a Cancer of the Muscle Lineage Gryder, Berkley E. Wachtel, Marco Chang, Kenneth El Demerdash, Osama Aboreden, Nicholas G. Mohammed, Wardah Ewert, Winston Pomella, Silvia Rota, Rossella Wei, Jun S. Song, Young Stanton, Benjamin Z. Schäfer, Beat Vakoc, Christopher R. Khan, Javed iScience Article Core regulatory transcription factors (CR TFs) establish enhancers with logical ordering during embryogenesis and development. Here we report that in fusion-positive rhabdomyosarcoma, a cancer of the muscle lineage, the chief oncogene PAX3-FOXO1 is driven by a translocated FOXO1 super enhancer (SE) restricted to a late stage of myogenesis. Using chromatin conformation capture techniques, we demonstrate that the extensive FOXO1 cis-regulatory domain interacts with PAX3. Furthermore, RNA sequencing and chromatin immunoprecipitation sequencing data in tumors bearing rare PAX translocations implicate enhancer miswiring across all fusion-positive tumors. HiChIP of H3K27ac showed connectivity between the FOXO1 SE, additional intra-domain enhancers, and the PAX3 promoter. We show that PAX3-FOXO1 transcription is diminished when this network of enhancers is ablated by CRISPR. Our data reveal a hijacked enhancer network that disrupts the stepwise CR TF logic of normal skeletal muscle development (PAX3 to MYOD to MYOG), replacing it with an “infinite loop” enhancer logic that locks rhabdomyosarcoma in an undifferentiated stage. Elsevier 2020-04-29 /pmc/articles/PMC7226896/ /pubmed/32416589 http://dx.doi.org/10.1016/j.isci.2020.101103 Text en http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gryder, Berkley E.
Wachtel, Marco
Chang, Kenneth
El Demerdash, Osama
Aboreden, Nicholas G.
Mohammed, Wardah
Ewert, Winston
Pomella, Silvia
Rota, Rossella
Wei, Jun S.
Song, Young
Stanton, Benjamin Z.
Schäfer, Beat
Vakoc, Christopher R.
Khan, Javed
Miswired Enhancer Logic Drives a Cancer of the Muscle Lineage
title Miswired Enhancer Logic Drives a Cancer of the Muscle Lineage
title_full Miswired Enhancer Logic Drives a Cancer of the Muscle Lineage
title_fullStr Miswired Enhancer Logic Drives a Cancer of the Muscle Lineage
title_full_unstemmed Miswired Enhancer Logic Drives a Cancer of the Muscle Lineage
title_short Miswired Enhancer Logic Drives a Cancer of the Muscle Lineage
title_sort miswired enhancer logic drives a cancer of the muscle lineage
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7226896/
https://www.ncbi.nlm.nih.gov/pubmed/32416589
http://dx.doi.org/10.1016/j.isci.2020.101103
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