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Multiple interactions of the oncoprotein transcription factor MYC with the SWI/SNF chromatin remodeler
The SNF5 subunit of the SWI/SNF chromatin remodeling complex has been shown to act as a tumor suppressor through multiple mechanisms, including impairing the ability of the oncoprotein transcription factor MYC to bind chromatin. Beyond SNF5, however, it is unknown to what extent MYC can access addit...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8141032/ https://www.ncbi.nlm.nih.gov/pubmed/33931740 http://dx.doi.org/10.1038/s41388-021-01804-7 |
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author | Woodley, Chase M. Romer, Alexander S. Wang, Jing Guarnaccia, Alissa D. Elion, David L. Maxwell, Jack N. Guerrazzi, Kiana McCann, Tyler S. Popay, Tessa M. Matlock, Brittany K. Flaherty, David K. Lorey, Shelly L. Liu, Qi Tansey, William P. Weissmiller, April M. |
author_facet | Woodley, Chase M. Romer, Alexander S. Wang, Jing Guarnaccia, Alissa D. Elion, David L. Maxwell, Jack N. Guerrazzi, Kiana McCann, Tyler S. Popay, Tessa M. Matlock, Brittany K. Flaherty, David K. Lorey, Shelly L. Liu, Qi Tansey, William P. Weissmiller, April M. |
author_sort | Woodley, Chase M. |
collection | PubMed |
description | The SNF5 subunit of the SWI/SNF chromatin remodeling complex has been shown to act as a tumor suppressor through multiple mechanisms, including impairing the ability of the oncoprotein transcription factor MYC to bind chromatin. Beyond SNF5, however, it is unknown to what extent MYC can access additional SWI/SNF subunits or how these interactions affect the ability of MYC to drive transcription particularly in SNF5-null cancers. Here, we report that MYC interacts with multiple SWI/SNF components independent of SNF5. We show that MYC binds the pan-SWI/SNF subunit BAF155 through the BAF155 SWIRM domain, an interaction that is inhibited by the presence of SNF5. In SNF5-null cells, MYC binds with remaining SWI/SNF components to essential genes, although for a purpose that is distinct from chromatin remodeling. Analysis of MYC–SWI/SNF target genes in SNF5-null cells reveals that they are associated with core biological functions of MYC linked to protein synthesis. These data reveal that MYC can bind SWI/SNF in a SNF5-independent manner and that SNF5 modulates access of MYC to core SWI/SNF complexes. This work provides a framework in which to interrogate the influence of SWI/SNF on MYC function in cancers in which SWI/SNF or MYC are altered. |
format | Online Article Text |
id | pubmed-8141032 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
record_format | MEDLINE/PubMed |
spelling | pubmed-81410322021-10-30 Multiple interactions of the oncoprotein transcription factor MYC with the SWI/SNF chromatin remodeler Woodley, Chase M. Romer, Alexander S. Wang, Jing Guarnaccia, Alissa D. Elion, David L. Maxwell, Jack N. Guerrazzi, Kiana McCann, Tyler S. Popay, Tessa M. Matlock, Brittany K. Flaherty, David K. Lorey, Shelly L. Liu, Qi Tansey, William P. Weissmiller, April M. Oncogene Article The SNF5 subunit of the SWI/SNF chromatin remodeling complex has been shown to act as a tumor suppressor through multiple mechanisms, including impairing the ability of the oncoprotein transcription factor MYC to bind chromatin. Beyond SNF5, however, it is unknown to what extent MYC can access additional SWI/SNF subunits or how these interactions affect the ability of MYC to drive transcription particularly in SNF5-null cancers. Here, we report that MYC interacts with multiple SWI/SNF components independent of SNF5. We show that MYC binds the pan-SWI/SNF subunit BAF155 through the BAF155 SWIRM domain, an interaction that is inhibited by the presence of SNF5. In SNF5-null cells, MYC binds with remaining SWI/SNF components to essential genes, although for a purpose that is distinct from chromatin remodeling. Analysis of MYC–SWI/SNF target genes in SNF5-null cells reveals that they are associated with core biological functions of MYC linked to protein synthesis. These data reveal that MYC can bind SWI/SNF in a SNF5-independent manner and that SNF5 modulates access of MYC to core SWI/SNF complexes. This work provides a framework in which to interrogate the influence of SWI/SNF on MYC function in cancers in which SWI/SNF or MYC are altered. 2021-04-30 2021-05 /pmc/articles/PMC8141032/ /pubmed/33931740 http://dx.doi.org/10.1038/s41388-021-01804-7 Text en http://www.nature.com/authors/editorial_policies/license.html#termsUsers 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 Woodley, Chase M. Romer, Alexander S. Wang, Jing Guarnaccia, Alissa D. Elion, David L. Maxwell, Jack N. Guerrazzi, Kiana McCann, Tyler S. Popay, Tessa M. Matlock, Brittany K. Flaherty, David K. Lorey, Shelly L. Liu, Qi Tansey, William P. Weissmiller, April M. Multiple interactions of the oncoprotein transcription factor MYC with the SWI/SNF chromatin remodeler |
title | Multiple interactions of the oncoprotein transcription factor MYC with the SWI/SNF chromatin remodeler |
title_full | Multiple interactions of the oncoprotein transcription factor MYC with the SWI/SNF chromatin remodeler |
title_fullStr | Multiple interactions of the oncoprotein transcription factor MYC with the SWI/SNF chromatin remodeler |
title_full_unstemmed | Multiple interactions of the oncoprotein transcription factor MYC with the SWI/SNF chromatin remodeler |
title_short | Multiple interactions of the oncoprotein transcription factor MYC with the SWI/SNF chromatin remodeler |
title_sort | multiple interactions of the oncoprotein transcription factor myc with the swi/snf chromatin remodeler |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8141032/ https://www.ncbi.nlm.nih.gov/pubmed/33931740 http://dx.doi.org/10.1038/s41388-021-01804-7 |
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