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Histone Modification02:32

Histone Modification

16.1K
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...
16.1K
Histone Modification02:32

Histone Modification

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No description available
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Histone Variants at the Centromere02:30

Histone Variants at the Centromere

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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...
5.0K
Phase II Reactions: Acetylation Reactions01:24

Phase II Reactions: Acetylation Reactions

800
Acetylation, a phase II biotransformation reaction, introduces an acetyl group to drugs or their metabolites. Acetyltransferase enzymes facilitate this reaction, which resembles α-amino acid conjugation due to the addition of a functional group to the drug molecule.
The substrates for acetylation are typically drugs or their metabolites with an amino, sulfonamide, or hydrazine functional group. Acetylation can occur at several points in the drug molecule, including primary, secondary, and...
800
DNA Microarrays02:34

DNA Microarrays

21.1K
Microarrays are high-throughput and relatively inexpensive assays that can be automated to analyze large quantities of data at a time. They are used in genome-wide studies to compare gene or protein expression under two varied conditions, such as healthy and diseased states. Microarrays consist of glass or silica slides on which probe molecules are covalently attached through surface functionalization. Most commonly, the slides are prepared through the chemisorption of silanes to silica...
21.1K
Covalently Linked Protein Regulators02:04

Covalently Linked Protein Regulators

9.4K
Proteins can undergo many types of post-translational modifications, often in response to changes in their environment. These modifications play an important role in the function and stability of these proteins. Covalently linked molecules include functional groups, such as methyl, acetyl, and phosphate groups, and also small proteins, such as ubiquitin. There are around 200 different types of covalent regulators that have been identified.
These groups modify specific amino acids in a protein....
9.4K

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Updated: Jan 29, 2026

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Genomewide histone acetylation microarrays.

Daniel Robyr1, Michael Grunstein

  • 1Department of Biological Chemistry, UCLA School of Medicine and the Molecular Biology Institute, Boyer Hall, University of California, Los Angeles, CA 90095, USA.

Methods (San Diego, Calif.)
|August 2, 2003
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Summary
This summary is machine-generated.

This study introduces a rapid method to analyze histone modifications across the entire genome. By combining chromatin immunoprecipitation (ChIP) with DNA microarrays, researchers can uncover broad chromosomal patterns of gene regulation.

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Area of Science:

  • Molecular Biology
  • Epigenetics
  • Genomics

Background:

  • Histone modifications like acetylation and methylation are key regulators of gene activity.
  • Chromatin immunoprecipitation (ChIP) enables the study of specific histone modifications at genes.
  • Previous methods were limited to analyzing individual genes, potentially missing broader patterns.

Purpose of the Study:

  • To develop a rapid, genome-wide approach for studying histone modifications.
  • To investigate chromosomal patterns of histone modification.
  • To advance the understanding of epigenetic regulation.

Main Methods:

  • Combining chromatin immunoprecipitation (ChIP) with DNA microarrays.
  • Enabling the analysis of various histone modifications, including acetylation, methylation, phosphorylation, and ubiquitination.
  • Facilitating the study of histone modifications genome-wide.

Main Results:

  • A novel approach for rapid, genome-wide analysis of histone modifications was established.
  • The method allows for the identification of chromosomal patterns of histone modification.
  • This technique provides a broader view of epigenetic regulation compared to gene-specific studies.

Conclusions:

  • The described method significantly enhances the ability to study histone modifications across the genome.
  • This approach facilitates the discovery of novel insights into gene regulation and epigenetic mechanisms.
  • Future studies can leverage this technique to explore other histone modifications and their roles in biological processes.