肌发生
MyoD公司
背景(考古学)
细胞生物学
增强子
转录因子
C2C12型
心肌细胞
化学
生物
生物化学
基因
古生物学
作者
Mónika Gönczi,João Miguel Correia Teixeira,Susana Barrera-Vilarmau,Laura Mediani,Francesco Antoniani,Tamás Milán Nagy,Krisztina Fehér,Zsolt Ráduly,Viktor Ambrus,József Tőzsér,Endre Barta,Katalin E. Kövér,László Csernoch,Serena Carra,Mónika Fuxreiter
标识
DOI:10.1038/s41467-023-37017-7
摘要
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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