An Embryonic Stem Cell-Specific NuRD Complex Functions through Interaction with WDR5

被引:20
作者
Ee, Ly-Sha [1 ]
McCannell, Kurtis N. [1 ]
Tang, Yang [2 ]
Fernandes, Nancy [2 ]
Hardy, W. Rod [1 ]
Green, Michael R. [1 ,3 ]
Chu, Feixia [2 ]
Fazzio, Thomas G. [1 ]
机构
[1] Univ Massachusetts, Med Sch, Dept Mol Cell & Canc Biol, Worcester, MA 01605 USA
[2] Univ New Hampshire, Dept Mol Cellular & Biomed Sci, Durham, NH 03824 USA
[3] Univ Massachusetts, Med Sch, Howard Hughes Med Inst, Worcester, MA 01605 USA
来源
STEM CELL REPORTS | 2017年 / 8卷 / 06期
关键词
CORE TRANSCRIPTIONAL NETWORK; LINEAGE LEUKEMIA PROTEIN-1; HISTONE H3; MOLECULAR RECOGNITION; STRUCTURAL BASIS; ACTIVE GENES; PLURIPOTENCY; DEACETYLASE; METHYLATION; MBD3;
D O I
10.1016/j.stemcr.2017.04.020
中图分类号
Q813 [细胞工程];
学科分类号
摘要
The Nucleosome Remodeling and Deacetylase (NuRD) complex is a chromatin regulatory complex that functions as a transcriptional corepressor in metazoans. The NuRD subunit MBD3 is essential for targeting and assembly of a functional NuRD complex as well as embryonic stem cell (ESC) pluripotency. Three MBD3 isoforms (MBD3A, MBD3B, and MBD3C) are expressed in mouse. Here, we find that the MBD3C isoform contains a unique 50-amino-acid N-terminal region that is necessary for MBD3C to specifically interact with the histone H3 binding protein WDR5. Domain analyses of WDR5 reveal that the H3 binding pocket is required for interaction with MBD3C. We find that while Mbd3c knockout ESCs differentiate normally, MBD3C is redundant with the MBD3A and MBD3B isoforms in regulation of gene expression, with the unique MBD3C N terminus required for this redundancy. Together, our data characterize a unique NuRD complex variant that functions specifically in ESCs.
引用
收藏
页码:1488 / 1496
页数:9
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