A Complex with Chromatin Modifiers That Occupies E2F- and Myc-Responsive Genes in G0 Cells

By Hidesato Ogawa, K. Ishiguro, S. Gaubatz, D. Livingston, Y. Nakatani. Science, 2002

835 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/06f430dce7ac13e6faf24a2190843b587cea6866

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Citations in the corpus

Histone and chromatin cross-talk. (2003, background): “recently, it was shown that several transcription factors are able to recruit proteins or protein complexes containing HMT activity to specific sites of the genome ([65–67].”
Coordinated histone modifications mediated by a CtBP co-repressor complex (2003, methodology): “To understand how CtBP represses transcription, we undertook the biochemical purification of CtB”
Transcriptional regulation by Polycomb group proteins (2013, background): “; and from the Novo Nordisk Foundation, the Danish Cancer Society and the Danish Council for Strategic Research (12-110503) to K.”
An epigenetic road map for histone lysine methylation (2003, background): “Recruitment of several H3-K9-specific HMTases induces gene repression within euchromatin (Tachibana et al., 2001; Nielsen et al., 2001; Vandel et al., 2001; Ogawa et al., 2002; Schultz et al., 2002; Tachibana et al., 2002; Yang et al., 2002).”
The E2F transcriptional network: old acquaintances with new faces (2005, background): “Consistent with these observations, an E2F6 containing chromatin-modifying complex was detected at cell cycle-regulated promoters in G0 cells (Ogawa et al., 2002).”
Histone methyltransferases G9a and GLP form heteromeric complexes and are both crucial for methylation of euchromatin at H3-K9. (2005, background): “Recent biochemical studies have shown that several transcriptional silencing complexes, such as E2F6 (Ogawa et al. 2002), CtBP-1 (Shi et al. 2003), and CDP/cut (Nishio and Walsh 2004), contained not only G9a but also Eu-HMTase1.”
The E2F family: specific functions and overlapping interests (2004, background): “E2F6 is known to interact, and form complexes with, the Polycomb Group (PcG) proteins, but it is not yet clear if these interactions are required to regulate its activity (Trimarchi et al, 2001; Ogawa et al, 2002).”
Pocket proteins and cell cycle control (2005, background): “Whereas SUV39H1 is a H3K9 trimethylase that is implicated in transcriptional silencing, Eu-HMTase1 is homologous to the ‘G9a’ H3K9 mono- and dimethylase (Peters et al., 2003; Rice et al., 2003) and is implicated in reversible promoter repression (Ogawa et al., 2002).”
Variant PRC1 Complex-Dependent H2A Ubiquitylation Drives PRC2 Recruitment and Polycomb Domain Formation (2014, background): “The catalytic core of PRC1 consists of RING1A or RING1B, which dimerize with one of six PCGFprotein partners (PCGF1-6) that regulate assembly of specific PRC1 complexes (Buchwald et al., 2006; Chamberlain et al., 2008; Farcas et al., 2012; Gao et al., 2012; Gearhart et al., 2006; Li et al., 2006; Og”