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Alternatively spliced exon regulates context-dependent MEF2D higher-order assembly during myogenesis

During muscle cell differentiation, the alternatively spliced, acidic β-domain potentiates transcription of Myocyte-specific Enhancer Factor 2 (Mef2D). Sequence analysis by the FuzDrop method indicates that the β-domain can serve as an interaction element for Mef2D higher-order assembly. In accord,...

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Autores principales: Gönczi, Mónika, Teixeira, João M. C., Barrera-Vilarmau, Susana, Mediani, Laura, Antoniani, Francesco, Nagy, Tamás Milán, Fehér, Krisztina, Ráduly, Zsolt, Ambrus, Viktor, Tőzsér, József, Barta, Endre, Kövér, Katalin E., Csernoch, László, Carra, Serena, Fuxreiter, Monika
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10006080/
https://www.ncbi.nlm.nih.gov/pubmed/36898987
http://dx.doi.org/10.1038/s41467-023-37017-7
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author Gönczi, Mónika
Teixeira, João M. C.
Barrera-Vilarmau, Susana
Mediani, Laura
Antoniani, Francesco
Nagy, Tamás Milán
Fehér, Krisztina
Ráduly, Zsolt
Ambrus, Viktor
Tőzsér, József
Barta, Endre
Kövér, Katalin E.
Csernoch, László
Carra, Serena
Fuxreiter, Monika
author_facet Gönczi, Mónika
Teixeira, João M. C.
Barrera-Vilarmau, Susana
Mediani, Laura
Antoniani, Francesco
Nagy, Tamás Milán
Fehér, Krisztina
Ráduly, Zsolt
Ambrus, Viktor
Tőzsér, József
Barta, Endre
Kövér, Katalin E.
Csernoch, László
Carra, Serena
Fuxreiter, Monika
author_sort Gönczi, Mónika
collection PubMed
description During muscle cell differentiation, the alternatively spliced, acidic β-domain potentiates transcription of Myocyte-specific Enhancer Factor 2 (Mef2D). Sequence analysis by the FuzDrop method indicates that the β-domain can serve as an interaction element for Mef2D higher-order assembly. In accord, we observed Mef2D mobile nuclear condensates in C2C12 cells, similar to those formed through liquid-liquid phase separation. In addition, we found Mef2D solid-like aggregates in the cytosol, the presence of which correlated with higher transcriptional activity. In parallel, we observed a progress in the early phase of myotube development, and higher MyoD and desmin expression. In accord with our predictions, the formation of aggregates was promoted by rigid β-domain variants, as well as by a disordered β-domain variant, capable of switching between liquid-like and solid-like higher-order states. Along these lines, NMR and molecular dynamics simulations corroborated that the β-domain can sample both ordered and disordered interactions leading to compact and extended conformations. These results suggest that β-domain fine-tunes Mef2D higher-order assembly to the cellular context, which provides a platform for myogenic regulatory factors and the transcriptional apparatus during the developmental process.
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spelling pubmed-100060802023-03-12 Alternatively spliced exon regulates context-dependent MEF2D higher-order assembly during myogenesis Gönczi, Mónika Teixeira, João M. C. Barrera-Vilarmau, Susana Mediani, Laura Antoniani, Francesco Nagy, Tamás Milán Fehér, Krisztina Ráduly, Zsolt Ambrus, Viktor Tőzsér, József Barta, Endre Kövér, Katalin E. Csernoch, László Carra, Serena Fuxreiter, Monika Nat Commun Article During muscle cell differentiation, the alternatively spliced, acidic β-domain potentiates transcription of Myocyte-specific Enhancer Factor 2 (Mef2D). Sequence analysis by the FuzDrop method indicates that the β-domain can serve as an interaction element for Mef2D higher-order assembly. In accord, we observed Mef2D mobile nuclear condensates in C2C12 cells, similar to those formed through liquid-liquid phase separation. In addition, we found Mef2D solid-like aggregates in the cytosol, the presence of which correlated with higher transcriptional activity. In parallel, we observed a progress in the early phase of myotube development, and higher MyoD and desmin expression. In accord with our predictions, the formation of aggregates was promoted by rigid β-domain variants, as well as by a disordered β-domain variant, capable of switching between liquid-like and solid-like higher-order states. Along these lines, NMR and molecular dynamics simulations corroborated that the β-domain can sample both ordered and disordered interactions leading to compact and extended conformations. These results suggest that β-domain fine-tunes Mef2D higher-order assembly to the cellular context, which provides a platform for myogenic regulatory factors and the transcriptional apparatus during the developmental process. Nature Publishing Group UK 2023-03-10 /pmc/articles/PMC10006080/ /pubmed/36898987 http://dx.doi.org/10.1038/s41467-023-37017-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Gönczi, Mónika
Teixeira, João M. C.
Barrera-Vilarmau, Susana
Mediani, Laura
Antoniani, Francesco
Nagy, Tamás Milán
Fehér, Krisztina
Ráduly, Zsolt
Ambrus, Viktor
Tőzsér, József
Barta, Endre
Kövér, Katalin E.
Csernoch, László
Carra, Serena
Fuxreiter, Monika
Alternatively spliced exon regulates context-dependent MEF2D higher-order assembly during myogenesis
title Alternatively spliced exon regulates context-dependent MEF2D higher-order assembly during myogenesis
title_full Alternatively spliced exon regulates context-dependent MEF2D higher-order assembly during myogenesis
title_fullStr Alternatively spliced exon regulates context-dependent MEF2D higher-order assembly during myogenesis
title_full_unstemmed Alternatively spliced exon regulates context-dependent MEF2D higher-order assembly during myogenesis
title_short Alternatively spliced exon regulates context-dependent MEF2D higher-order assembly during myogenesis
title_sort alternatively spliced exon regulates context-dependent mef2d higher-order assembly during myogenesis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10006080/
https://www.ncbi.nlm.nih.gov/pubmed/36898987
http://dx.doi.org/10.1038/s41467-023-37017-7
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