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Related Concept Videos

Histone Modification02:32

Histone Modification

The histone proteins have a flexible N-terminal tail extending out from the nucleosome. These histone tails are often subjected to post-translational modifications such as acetylation, methylation, phosphorylation, and ubiquitination. Particular combinations of these modifications form “histone codes” that influence the chromatin folding and tissue-specific gene expression.
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone deacetylase,...
Histone Modification02:32

Histone Modification

The histone proteins have a flexible N-terminal tail extending out from the nucleosome. These histone tails are often subjected to post-translational modifications such as acetylation, methylation, phosphorylation, and ubiquitination. Particular combinations of these modifications form “histone codes” that influence the chromatin folding and tissue-specific gene expression.
Acetylation
The enzyme histone acetyltransferase adds acetyl group to the histones. Another enzyme, histone deacetylase,...
Spreading of Chromatin Modifications02:25

Spreading of Chromatin Modifications

The histone proteins in the nucleosomes are post-translationally modified (PTM) to increase or decrease access to DNA. The commonly observed PTMs are methylation, acetylation, phosphorylation, and ubiquitination of lysine amino acids in the histone H3 tail region. These histone modifications have specific meaning for the cell. Hence, they are called "histone code". The protein complex involved in histone modification is termed as "reader-writer" complex.
Writers
The writer is an enzyme that can...
Histone Variants at the Centromere02:30

Histone Variants at the Centromere

Histone variants are the histone proteins with structural and sequence variations. These variants may be regarded as “mutant” forms that replace their canonical histone counterparts in the nucleosomes. Specific post-translational modifications on the histone variants enable further chromatin complexity and regulate tissue-specific gene expression. The most common histone variants are from histone H2A, H2B, and linker histone H1 families. However, several variants of histone H3 variants are also...
The Nucleosome Core Particle02:10

The Nucleosome Core Particle

Nucleosomes are the DNA-histone complex, where the DNA strand is wound around the histone core. The histone core is an octamer containing two copies of H2A, H2B, H3, and H4 histone proteins.
The paradox
Nucleosomes, paradoxically, perform two opposite functions simultaneously. On the one hand, their main responsibility is to protect the delicate DNA strands from physical damage and help achieve a higher compaction ratio. While on the other hand, they must allow polymerase enzymes to access DNA...
The Nucleosome Core Particle01:12

The Nucleosome Core Particle

Nucleosomes are the DNA-histone complex, where the DNA strand is wound around the histone core. The histone core is an octamer containing two copies of H2A, H2B, H3, and H4 histone proteins.
Nucleosomes, paradoxically, perform two opposite functions simultaneously. On the one hand, their primary aim is to protect the delicate DNA strands from physical damage and help achieve a higher compaction ratio. On the other hand, they must allow polymerase enzymes to access histone-bound DNA during...

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Updated: May 10, 2026

Unveiling Histone Proteoforms using 2D-TAU Gel Electrophoresis
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Toward breaking the histone code: bayesian graphical models for histone modifications.

Riten Mitra1, Peter Müller, Shoudan Liang

  • 1ICES, University of Texas at Austin, USA.

Circulation. Cardiovascular Genetics
|June 11, 2013
PubMed
Summary
This summary is machine-generated.

This study introduces a Bayesian graphical model to decode histone modification networks and their functional roles in different genomic regions. The approach reveals how histone networks differ across genomic locations, linking histone patterns to gene regulation.

Keywords:
epigenomicsgene expression regulationgraphmodels, statisticalnetworknucleosomesstatistics

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Area of Science:

  • Epigenetics and Genomics
  • Computational Biology
  • Molecular Biology

Background:

  • Histones are core components of nucleosomes, organizing DNA.
  • Histone modifications (HMs) are post-translational changes on histone tails.
  • Combinatorial patterns of HMs, or histone codes, regulate biological processes.

Purpose of the Study:

  • To decode the complex biological network of histone modifications within specific genomic regions.
  • To demonstrate how histone modification networks vary across different regulatory genomic regions.
  • To establish a link between histone network attributes and genomic functions.

Main Methods:

  • Development of a Bayesian graphical model for probabilistic inference of HM dependence patterns.
  • Utilizing posterior inference to compute probabilities of distinct HM dependence patterns via graphs.
  • Application of differential network analysis to compare HM networks across different genomic locations.

Main Results:

  • The Bayesian model successfully inferred histone modification networks from ChIP-Seq data.
  • Differential network analyses provided insights into the coregulation of HMs in various genomic regions.
  • The study confirmed existing findings and generated new hypotheses regarding histone codes.

Conclusions:

  • Bayesian graphical models offer a powerful framework for inferring histone networks.
  • Borrowing strength across conditions enhances the power to detect differences in histone networks.
  • This approach links histone modification patterns to genomic functions.