E-GEOD-20213 - ChIP for H3K27me3 in Murine ES Cells: wild type and Ring1B-/- cells

Released on 14 May 2010, last updated on 1 May 2014
Mus musculus
Samples (20)
Array (1)
Protocols (8)
Native ChIP on chip for H3K27me3 in murine ES cells comparing WT and Ring1B-/- cells. Paper Abstract: How polycomb group proteins repress gene expression in vivo is not known. Whilst histone modifying activities of the polycomb repressive complexes have been studied extensively, in vitro data has suggested a direct activity of the PRC1 complex in compacting chromatin. Here, we investigate higher-order chromatin compaction of polycomb targets in vivo. We show that polycomb repressive complexes are required to maintain a compact chromatin state at Hox loci in embryonic stem (ES) cells. There is specific decompaction in the absence of PRC2 or PRC1. This is due to PRC1, since decompaction occurs in Ring1B null cells that still have PRC2-mediated H3K27 methylation. Moreover, we show that the ability of Ring1B to restore a compact chromatin state, and to repress Hox gene expression in ES cells, is not dependent on its histone ubiquitination activity. We suggest that Ring1B-mediated chromatin compaction acts to directly limit transcription in vivo. Biological replicates: 3 independently grown, harvested,preplated, micrococcal nuclease digested and ChIP for H3K27me3. 5 Technical replicates.
Experiment type
ChIP-chip by tiling array 
Graeme Richard Grimes <Graeme.Grimes@hgu.mrc.ac.uk>, Graeme R Grimes, Ragnhild Eskeland, Wendy A Bickmore
Ring1B compacts chromatin structure and represses gene expression independent of histone ubiquitination. Eskeland R, Leeb M, Grimes GR, Kress C, Boyle S, Sproul D, Gilbert N, Fan Y, Skoultchi AI, Wutz A, Bickmore WA. , Europe PMC 20471950
Investigation descriptionE-GEOD-20213.idf.txt
Sample and data relationshipE-GEOD-20213.sdrf.txt
Raw data (1)E-GEOD-20213.raw.1.zip
Processed data (1)E-GEOD-20213.processed.1.zip
Array designA-GEOD-10011.adf.txt