Nature Communications (Feb 2024)

Matrin3 mediates differentiation through stabilizing chromatin loop-domain interactions and YY1 mediated enhancer-promoter interactions

  • Tianxin Liu,
  • Qian Zhu,
  • Yan Kai,
  • Trevor Bingham,
  • Stacy Wang,
  • Hye Ji Cha,
  • Stuti Mehta,
  • Thorsten M. Schlaeger,
  • Guo-Cheng Yuan,
  • Stuart H. Orkin

DOI
https://doi.org/10.1038/s41467-024-45386-w
Journal volume & issue
Vol. 15, no. 1
pp. 1 – 18

Abstract

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Abstract Although emerging evidence indicates that alterations in proteins within nuclear compartments elicit changes in chromosomal architecture and differentiation, the underlying mechanisms are not well understood. Here we investigate the direct role of the abundant nuclear complex protein Matrin3 (Matr3) in chromatin architecture and development in the context of myogenesis. Using an acute targeted protein degradation platform (dTAG-Matr3), we reveal the dynamics of development-related chromatin reorganization. High-throughput chromosome conformation capture (Hi-C) experiments revealed substantial chromatin loop rearrangements soon after Matr3 depletion. Notably, YY1 binding was detected, accompanied by the emergence of novel YY1-mediated enhancer-promoter loops, which occurred concurrently with changes in histone modifications and chromatin-level binding patterns. Changes in chromatin occupancy by Matr3 also correlated with these alterations. Overall, our results suggest that Matr3 mediates differentiation through stabilizing chromatin accessibility and chromatin loop-domain interactions, and highlight a conserved and direct role for Matr3 in maintenance of chromosomal architecture.