Histone and chromatin cross-talk.

By W. Fischle, Yanming Wang, C. D. Allis. Current Opinion in Cell Biology, 2003

1,243 citations recorded by the source corpus.

View Paper: https://www.semanticscholar.org/paper/564334d818d68100500189c2093a62ee9af59998

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

In Molecular Biology

Citations in the corpus

Rhythmic CLOCK-BMAL1 binding to multiple E-box motifs drives circadian Dbp transcription and chromatin transitions (2006, positive): “To this end, we used ChIP experiments to examine for the presence of signatures diagnostic for transcriptionally permissive chromatin, such as acetylation of Lys9 (H3-K9) and trimethylation of Lys4 (H3-K4) within histone H3, and for signatures diagnostic for transcriptionally inert chromatin, such a”
The SET-domain protein superfamily: protein lysine methyltransferases (2005, background): “These tails are subject to several post-translational covalent modifications, including acetylation, phosphorylation, ubiquitination, sumoylation and methylation (reviewed in [1]).”
Non-commercial Research and Educational Use including without Limitation Use in Instruction at Your Institution, Sending It to Specific Colleagues That You Know, and Providing a Copy to Your Institution's Administrator. All Other Uses, Reproduction and Distribution, including without Limitation Comm (2005, neutral): “(4) it is clear that the dipolar couplings depend on geometrical information about the solute and on a maximum of five independent order parameters.”
From silencing to gene expression: real-time analysis in single cells. (2004, background): “Lysine residues in histone tails can be either mono-, di- or Introduction trimethylated (reviewed, Fischle et al., 2003) and a number of histone H3 K9 methyltransferases (HMTases) have Genes are expressed as a result of the concerted probeen identified (reviewed, Marmorstein, 2003). cesses of…”
REST and its corepressors mediate plasticity of neuronal gene chromatin throughout neurogenesis. (2005, background): “Because this modification is associated with DNA methylation (Bird, 2002) and silencing (reviewed in Bannister et al. [2002] and Fischle et al. [2003] ), we examined the methylation status of the RE1 site.”
Phylogenomics of the nucleosome (2003, background): “These modifications would in turn have imposed a strict evolutionary constraint on the amino acid residues in the histone tails, which are essentially invariant, especially in H3 and H4 (see below”
Chromatin decondensation and nuclear reorganization of the HoxB locus upon induction of transcription. (2004, background): “They can act as binding sites for specific regulatory proteins (Fischle et al. 2003) and may directly affect higher-order chromatin structure and condensation (Tse et al. 1998; Wolffe and Hayes 1999; Carruthers and Hansen 2000; Wang et al. 2001).”
Molecular basis for the discrimination of repressive methyl-lysine marks in histone H3 by Polycomb and HP1 chromodomains. (2003, background): “These include dynamic marks permitting rapid changes in gene expression in response to physiological and environmental stimuli as well as more permanent indexing systems required for the passage of heritable patterns of epigenetic information from one cell generation to the next (Fischle et al. 2003”
Structural and Functional Conservation of the NuA4 Histone Acetyltransferase Complex from Yeast to Humans (2004, background): “Furthermore, specific histone modifications have been shown to regulate others, both on the same N-terminal tail and in a transhistone fashion ( 17 ).”
Erasers of histone acetylation: the histone deacetylase enzymes. (2014, background): “One of the best studied examples of histone modification cross talk occurs between acetylation and methylation (Fischle et al. 2003).”
Phosphorylation of histone H3: a balancing act between chromosome condensation and transcriptional activation. (2004, background): “Acetylation and methylation of different lysine (Lys) and arginine residues in histones H3 and H4 have been linked to either transcriptionally active or transcriptionally repressed states of gene expression [ 10 ], whereas phosphorylation of histone H3 was initially linked to chromosome condensation”
Combinatorial patterns of histone acetylations and methylations in the human genome (2008, background): “It has been proposed that histone modifications can cross-tal”