Mmtr/dmap1, Tip-p400 Complex, Polycomb Repressive Complexes (Prcs), Bivalency, Poised Gene, Embryonic Stem Cells
Digital Object Identifier (DOI)
Chromatin remodeling, including histone modification, chromatin (un)folding, and nucleosome remodeling, is a significant transcriptional regulation mechanism. By these epigenetic modifications, transcription factors and their regulators are recruited to the promoters of target genes, and thus gene expression is controlled through either transcriptional activation or repression. The Mat1-mediated transcriptional repressor (MMTR)/DNA methyltransferase 1 (DNMT1)-associated protein (Dmap1) is a transcription corepressor involved in chromatin remodeling, cell cycle regulation, DNA double-strand break repair, and tumor suppression. The Tip60-p400 complex proteins, including MMTR/Dmap1, interact with the oncogene Myc in embryonic stem cells (ESCs). These proteins interplay with the stem cell-related proteome networks and regulate gene expressions. However, the detailed mechanisms of their functions are unknown. Here, we show that MMTR/Dmap1, along with other Tip60-p400 complex proteins, bind the promoters of differentiation commitment genes in mouse ESCs. Hence, MMTR/Dmap1 controls gene expression alterations during differentiation. Furthermore, we propose a novel mechanism of MMTR/Dmap1 function in early stage lineage commitment of mouse ESCs by crosstalk with the polycomb group (PcG) proteins. The complex controls histone mark bivalency and transcriptional poising of commitment genes. Taken together, our comprehensive findings will help better understand the MMTR/Dmap1-mediated transcriptional regulation in ESCs and other cell types.
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Citation / Publisher Attribution
Cells, v. 9, issue 5, art. 1190
Scholar Commons Citation
Lee, Young Jin; Son, Seung Han; Lim, Chang Su; Lee, Si Woo; Lee, Sangwoon; Jeon, Jinseon; Ha, Dae Hyun; Jung, Na Rae; Han, Su Youne; Do, Byung-Rok; Na, Insung; Uversky, Vladimir N.; and Kim, Chul Geun, "MMTR/Dmap1 Sets the Stage for Early Lineage Commitment of Embryonic Stem Cells by Crosstalk with PcG Proteins" (2020). Molecular Medicine Faculty Publications. 886.