Suz12 binds to silenced regions of the genome in a cell-type-specific manner

被引:255
作者
Squazzo, Sharon L.
O'Geen, Henriette
Komashko, Vitalina M.
Krig, Sheryl R.
Jin, Victor X.
Jang, Sung-wook
Margueron, Raphael
Reinberg, Danny
Green, Roland
Farnham, Peggy J. [1 ]
机构
[1] Univ Calif Davis, Dept Pharmacol, Davis, CA 95616 USA
[2] Univ Calif Davis, Genome Ctr, Davis, CA 95616 USA
[3] NimbleGen Syst Inc, Madison, WI 53711 USA
[4] Robert Wood Johnson Med Sch, Dept Biochem, Howard Hughes Med Inst, Div Nucle Acids Enzymol, Piscataway, NJ 08854 USA
[5] Univ Wisconsin, Grad Program Cellular & Mol Biol, Madison, WI 53706 USA
关键词
D O I
10.1101/gr.5306606
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Suzl2 is a component of the Polycomb group complexes 2, 3, and 4 (PRC 2/ 3/ 4). These complexes are critical for proper embryonic development, but very few target genes have been identified in either mouse or human cells. Using a variety of ChIP-chip approaches, we have identified a large set of Suz12 target genes in five different human and mouse cell lines. Interestingly, we found that Suz12 target promoters are cell type specific, with transcription factors and homeobox proteins predominating in embryonal cells and glycoproteins and immunoglobulin-related proteins predominating in adult tumors. We have also characterized the localization of other components of the PRC complex with Suz12 and investigated the overall relationship between Suz12 binding and markers of active versus inactive chromatin, using both promoter arrays and custom tiling arrays. Surprisingly, we find that the PRC complexes can be localized to discrete binding sites or spread through large regions of the mouse and human genomes. Finally, we have shown that some Suz12 target genes are bound by OCT4 in embryonal cells and suggest that OCT4 maintains stem cell self-renewal, in part, by recruiting PRC complexes to certain genes that promote differentiation.
引用
收藏
页码:890 / 900
页数:11
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