Transcription regulation by histone methylation: interplay between different covalent modifications of the core histone tails.

By Yi Zhang, D. Reinberg. Genes & Development, 2001

1,647 citations recorded by the source corpus.

Department of Biochemistry and Biophysics, Curriculum in Genetics and Molecular Biology, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, North Carolina 27599-7295, USA; Howard Hughes Medical Institute, Division of Nucleic Acids Enzymology, Department of Biochemistry, University of Medicine and Dentistry of New Jersey, Robert Wood Johnson Medical School, Piscataway, New Jersey 08854, USA

Subfields: Molecular Biology

View Paper: https://www.semanticscholar.org/paper/689d1ca87326f07b09be00dac044983677715877

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In Molecular Biology

1. Yi Zhang
2. D. Reinberg
3. C. D. Allis
4. S. Khorasanizadeh
5. Yang Shi
6. T. Jenuwein
7. A. Bird
8. Tony Kouzarides

Citations in the corpus

• The diverse functions of histone lysine methylation (2005, background): “Histone methylation occurs on arginine and lysine residues and is catalysed by enzymes belonging to three distinct families of proteins — the PRMT1 family, the SETDOMAIN -containing protein family, and the non-SET-domain proteins DOT1/DOT1L 3–6 .”
• DNA methylation patterns and epigenetic memory. (2002, background): “In mammalian and yeast systems, histone H3 Lys 9 methylation is associated with transcriptionally repressed heterochromatin (Bannister et al. 2001; Nakayama et al. 2001; Noma et al. 2001; Zhang and Reinberg 2001).”
• Histone H3 lysine 4 methylation is mediated by Set1 and required for cell growth and rDNA silencing in Saccharomyces cerevisiae. (2001, background): “Currently, it is not clear why Set1 is not active in a recombinant form compared with other recombinantly active histone methyltransferases, SUV39H1 family, G9a, and Set2 (for review, see Zhang and Reinberg 2001).”
• Review Histone Methylation: Dynamic or Static? (2002, background): “A stable methyl group also makes sense as part There are several documented cases in which active reversal of methylation may be deemed to be necessary, of an epigenetic mark for the inheritance of the silenced state following replication (Zhang and Reinberg, 2001).”
• Histone and chromatin cross-talk. (2003, background): “Similarly, arginines might be mono- or dimethylated (symmetric or asymmetric) [1,20].”
• G9a histone methyltransferase plays a dominant role in euchromatic histone H3 lysine 9 methylation and is essential for early embryogenesis. (2002, background): “In addition to acetylation and phosphorylation, methylation of histone tails at different residues has been implicated in transcriptional regulation (Jenuwein and Allis 2001; Zhang and Reinberg 2001).”
• The Roles of Post-translational Modifications in the Context of Protein Interaction Networks (2015, background): “Similar consideration apply to methylation events in histone [50] and other protein complexes [51].”
• RNA meets chromatin. (2005, background): “Relatively unstructured histone “tail” domains are exposed on the nucleosomal surface and are rich in post-translational modifications such as serine and threonine phosphorylation, lysine acetylation, lysine and arginine methylation, lysine ubiquitination and sumoylation, and ADPribosylation (Strahl”
• Dot1p modulates silencing in yeast by methylation of the nucleosome core. (2002, background): “The entire (3)H label was of AdoMet is a highly conserved glycine (Gly) in motif I recovered in the histone preparation and coeluted with (Zhang and Reinberg, 2001).”
• Reversal of histone lysine trimethylation by the JMJD2 family of histone demethylases. (2006, background): “Enzymes that are responsible for trimethylation at many of these sites have been identified (as reviewed in Margueron et al. [2005]; Sun et al., 2005; Zhang and Reinberg, 2001).”