Histone: Difference between revisions
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{{Short description|Proteins that package and order DNA into structural units}} | {{Short description|Proteins that package and order DNA into structural units}} | ||
{{Use dmy dates|date=October 2023}} | {{Use dmy dates|date=October 2023}} | ||
[[File:Nucleosome structure.png|thumb|right|250px|Assembly of histones into a nucleosome]] | |||
[[File:PDB 1kx3 EBI.jpg|thumb|right|250px|DNA on outside winding round histone on inside. View from top through helical axis]] | |||
Histones are highly alkaline proteins found in eukaryotic cell nuclei that package and order the DNA into structural units called [[nucleosomes]]. They are the chief protein components of [[chromatin]], acting as spools around which DNA winds, and play a role in gene regulation. | Histones are highly alkaline proteins found in eukaryotic cell nuclei that package and order the DNA into structural units called [[nucleosomes]]. They are the chief protein components of [[chromatin]], acting as spools around which DNA winds, and play a role in gene regulation. | ||
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* [[Gene expression]] | * [[Gene expression]] | ||
* [[DNA]] | * [[DNA]] | ||
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[[Category:Proteins]] | [[Category:Proteins]] | ||
[[Category:Epigenetics]] | [[Category:Epigenetics]] | ||
[[Category:Gene expression]] | [[Category:Gene expression]] | ||
Latest revision as of 15:50, 24 March 2025
Proteins that package and order DNA into structural units
Histones are highly alkaline proteins found in eukaryotic cell nuclei that package and order the DNA into structural units called nucleosomes. They are the chief protein components of chromatin, acting as spools around which DNA winds, and play a role in gene regulation.
Structure[edit]
Histones are composed of a core of eight proteins: two each of histone H2A, histone H2B, histone H3, and histone H4. This octamer forms the nucleosome core particle, around which approximately 147 base pairs of DNA are wrapped. The linker histone, histone H1, binds to the nucleosome and the linker DNA, helping to compact the nucleosome into higher-order structures.
Function[edit]
Histones play a critical role in the regulation of gene expression. By undergoing various post-translational modifications, such as methylation, acetylation, phosphorylation, and ubiquitination, histones can influence chromatin structure and function. These modifications can either promote or inhibit the transcription of genes, depending on the specific modification and the context in which it occurs.
Gene Regulation[edit]
Histone modifications are a key component of the epigenetic regulation of gene expression. For example, acetylation of histone tails is generally associated with transcriptional activation, as it reduces the positive charge on histones, decreasing their affinity for the negatively charged DNA and allowing transcription factors easier access to the DNA. Conversely, methylation can either activate or repress transcription, depending on which amino acids in the histone tails are methylated.
Histone Variants[edit]
In addition to the canonical histones, there are several histone variants that can replace the standard histones in the nucleosome. These variants can impart specific structural and functional properties to the chromatin. For example, the histone variant H2A.Z is involved in the regulation of gene expression and the maintenance of genome stability.
Role in Disease[edit]
Abnormal histone modifications and mutations in histone genes have been implicated in a variety of diseases, including cancer. For instance, mutations in the histone H3 gene have been associated with certain types of pediatric brain tumors. Additionally, the dysregulation of histone-modifying enzymes can lead to aberrant gene expression patterns that contribute to the development and progression of cancer.
Research and Therapeutic Implications[edit]
The study of histones and their modifications is a rapidly advancing field, with significant implications for understanding the mechanisms of gene regulation and the development of novel therapeutic strategies. Histone deacetylase inhibitors, for example, are being explored as potential treatments for cancer and other diseases characterized by dysregulated gene expression.
