Methylation of Histone H4 at Arginine 3 Facilitating Transcriptional Activation by Nuclear Hormone Receptor
By Hengbin Wang, Zhi‐Qing Huang, Li Xia, Qin Feng, H. Erdjument‐Bromage, Brian D. Strahl, S. Briggs, C. D. Allis, J. Wong, Paul Tempst and 1 more. Science, 2001
823 citations recorded by the source corpus.
Subfields: Molecular Biology
View Paper: https://www.semanticscholar.org/paper/ee2fc8a3852a4ece288b69bea2ccc0fd55b07dd2
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In Molecular Biology
- Yi Zhang
- D. Reinberg
- C. D. Allis
- S. Khorasanizadeh
- Paul Tempst
- H. Erdjument‐Bromage
- W. Fischle
- Yanming Wang
Citations in the corpus
- Histone demethylation by a family of JmjC domain-containing proteins (2006, methodology): “To prepare for 3 H-labelled methyl-histone octamers or oligonucleosome substrates, histone methyltransferase (HMT) assays were performed as previously described 13 .”
- The nucleosome: from genomic organization to genomic regulation. (2004, background): “Whereas residues adjacent to methyllysine 9 in the H3 peptide form backbone hydrogen hormone receptors (Wang et al., 2001).”
- Overview of Nomenclature of Nuclear Receptors (2006, background): “…that are structurally and functionally distinguishable from the p160 family and that contain ATP-dependent remodeling or histone arginine methyltransferase activities (Fryer and Archer, 1998; Dilworth et al., 2000; DiRenzo et al., 2000; Koh et al., 2001; Wang et al., 2001b; Xu et al., 2004).”
- Androgen receptor (AR) coregulators: a diversity of functions converging on and regulating the AR transcriptional complex. (2007, neutral): “AR-dependent gene expression via SRC proteins (92).”
- Histone and chromatin cross-talk. (2003, background): “contrast, acetylation of H4 on K8 and K12 by the HAT p300 is elevated after methylation of R3 [30].”
- Transcriptional complexes engaged by apo‐estrogen receptor‐α isoforms have divergent outcomes (2004, positive): “These data also confirm that PRMT1 methylates H4 R3 (Wang et al, 2001).”
- Human SWI/SNF-Associated PRMT5 Methylates Histone H3 Arginine 8 and Negatively Regulates Expression of ST7 and NM23 Tumor Suppressor Genes (2004, background): “It is important to note that PRMT5 also targets H4R3 (GRG), which is known to be methylated by the transcriptional activator PRMT1 (51).”