HDAC5

From WikiMD's Wellness Encyclopedia

HDAC5 (Histone Deacetylase 5) is an enzyme that in humans is encoded by the HDAC5 gene. This enzyme is a member of the histone deacetylase family, which plays a critical role in regulating transcription and cell cycle progression. HDAC5 is part of the class IIa HDACs, which are known for their involvement in various cellular processes including muscle differentiation, neuronal survival, and heart development.

Function[edit | edit source]

HDAC5 is involved in the modification of chromatin, which is crucial for regulating gene expression by deacetylating histone proteins. The removal of acetyl groups from histones leads to a more condensed chromatin structure and a reduction in gene expression levels. HDAC5 can shuttle between the nucleus and the cytoplasm, and its activity is regulated by various signals such as phosphorylation.

In the nucleus, HDAC5 represses transcription by forming complexes with other proteins, such as members of the myocyte enhancer factor-2 (MEF2) family. This interaction is important in muscle cell differentiation and adaptation. In the nervous system, HDAC5 has been implicated in the regulation of neuronal survival and plasticity.

Clinical Significance[edit | edit source]

Alterations in HDAC5 function have been associated with several human diseases, including cardiovascular diseases, neurodegenerative diseases, and cancer. For instance, overexpression of HDAC5 has been observed in certain types of cancer, suggesting a potential role in tumorigenesis. Conversely, HDAC5 has protective roles in the heart; its inhibition has been linked to cardiac hypertrophy and failure.

Research[edit | edit source]

HDAC5 is a target for the development of new therapeutic drugs. Inhibitors of HDAC5 are being studied for their potential to treat various diseases, including those related to aberrant histone deacetylation. Research in this area focuses on developing selective HDAC5 inhibitors that can modulate gene expression beneficially without causing the side effects associated with broad-spectrum HDAC inhibitors.

See Also[edit | edit source]


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Contributors: Prab R. Tumpati, MD