Target Name: MeCP1 histone deacetylase (HDAC) complex
NCBI ID: P16329
Review Report on MeCP1 histone deacetylase (HDAC) complex Target / Biomarker Content of Review Report on MeCP1 histone deacetylase (HDAC) complex Target / Biomarker
MeCP1 histone deacetylase (HDAC) complex
Other Name(s): None

Unlocking the Potential of MeCP1 Histone Deacetylase (HDAC) Complex as a Drug Target or Biomarker

Histone deacetylase (HDAC) is a key enzyme in the histone regulative pathway, which plays a critical role in cellular signaling, gene expression, and DNA replication. The HDAC enzyme has been implicated in various diseases, including cancer, neurodegenerative diseases, and developmental disorders. Therefore, targeting the HDAC pathway offers new avenues for therapeutic intervention. The MeCP1 histone deacetylase (HDAC) complex is a promising candidate for drug development due to its unique subcellular localization, structural complexity, and involvement in various cellular processes.

MeCP1 HDAC Complex

MeCP1 (Mammalian ears-associated protein 1) is a 21-kDa protein that is expressed in various tissues, including brain, heart, liver, and muscle. It is a key component of the nucleosome, which is the basic unit of chromatin, and is involved in the regulation of DNA replication, gene expression, and microtubule dynamics. The HDAC enzyme is a critical cofactor for MeCP1, allowing it to interact with chromatin and facilitate its functions.

The HDAC enzyme has three distinct subclasses: HDAC1, HDAC2, and HDAC3. Each subclass has a distinct catalytic mechanism and is involved in distinct cellular processes. For example, HDAC1 is involved in the regulation of DNA replication, while HDAC3 is involved in the regulation of cell growth and differentiation. The HDAC2 enzyme is responsible for the removal of acetyl groups from histones, which is a critical step in the histone regulative pathway.

MeCP1 HDAC Complex in Disease

The HDAC enzyme has been implicated in various diseases, including cancer, neurodegenerative diseases, and developmental disorders. In cancer, the HDAC enzyme has been shown to play a negative role in the regulation of cell cycle progression and the maintenance of cellular stability. Additionally, HDAC enzymes have been implicated in neurodegenerative diseases, including Alzheimer's disease, Parkinson's disease, and Huntington's disease, which are characterized by the progressive loss of brain cells and progressive cognitive decline.

Furthermore, the HDAC enzyme has also been implicated in developmental disorders, such as Down syndrome and Fragile X syndrome, which are characterized by the presence of specific genetic mutations that lead to the progressive loss of cellular structures and functions.

Drug Development

The MeCP1 HDAC complex offers a unique opportunity for drug development due to its subcellular localization and structural complexity. The HDAC enzyme is enriched in the nucleosome, which is the basic unit of chromatin, and is involved in the regulation of DNA replication, gene expression, and microtubule dynamics. Therefore, inhibiting the HDAC enzyme can lead to the disruption of these processes, which can have a significant impact on cellular behavior and function.

Several inhibitors have been shown to be effective in targeting the MeCP1 HDAC complex, including inhibitors that target the HDAC1 subclass (9), HDAC2 subclass (10), or HDAC3 subclass. These inhibitors have been shown to be effective in various cellular models, including cancer cell lines, neuroblastoma cells, and primary neurons, and have led to the inhibition of cellular processes, such as cell proliferation, migration, and invasion.

In addition to inhibitors, small molecules have also been shown to be effective in targeting the MeCP1 HDAC complex. These small molecules act by modulating the activity of the HDAC enzyme, leading to the disruption of its functions.

Conclusion

The MeCP1 HDAC complex is a promising candidate for drug development due to its unique subcellular localization, structural complexity, and involvement in various cellular processes. The inhibition of the HDAC enzyme has

Protein Name: MeCP1 Histone Deacetylase (HDAC) Complex

The "MeCP1 histone deacetylase (HDAC) complex Target / Biomarker Review Report" is a customizable review of hundreds up to thousends of related scientific research literature by AI technology, covering specific information about MeCP1 histone deacetylase (HDAC) complex comprehensively, including but not limited to:
•   general information;
•   protein structure and compound binding;
•   protein biological mechanisms;
•   its importance;
•   the target screening and validation;
•   expression level;
•   disease relevance;
•   drug resistance;
•   related combination drugs;
•   pharmacochemistry experiments;
•   related patent analysis;
•   advantages and risks of development, etc.
The report is helpful for project application, drug molecule design, research progress updates, publication of research papers, patent applications, etc. If you are interested to get a full version of this report, please feel free to contact us at BD@silexon.ai

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