Suz12 binds to silenced regions of the genome in a cell-type-specific manner
Autor: | Peggy J. Farnham, Henriette O'Geen, Victor X. Jin, Vitalina M. Komashko, Danny Reinberg, Sung Wook Jang, Sheryl R. Krig, Roland Green, Raphaël Margueron, Sharon L. Squazzo |
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Rok vydání: | 2006 |
Předmět: |
Genetic Markers
Chromatin Immunoprecipitation Letter Cellular differentiation Immunoglobulins Repressor Biology Mice Carcinoma Embryonal Genetics Animals Humans Gene Silencing Promoter Regions Genetic Gene Transcription factor Genetics (clinical) Glycoproteins Oligonucleotide Array Sequence Analysis Homeodomain Proteins Binding Sites Genome Tiling array Stem Cells Polycomb Repressive Complex 2 Gene Expression Regulation Developmental Cell Differentiation Promoter Molecular biology Chromatin Repressor Proteins Gene Targeting Octamer Transcription Factor-3 Chromatin immunoprecipitation Transcription Factors |
Zdroj: | Genome Research. 16:890-900 |
ISSN: | 1088-9051 |
Popis: | Suz12 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. |
Databáze: | OpenAIRE |
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