Chromatin accessibility complex 1

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Chromatin Accessibility Complex 1 (CHRAC1) is a protein complex that plays a crucial role in the regulation of gene expression by modulating the accessibility of chromatin to the transcription machinery. This complex is composed of several subunits, including the ATPase subunit ISWI, which is responsible for the energy-dependent remodeling of chromatin structure.

Structure and Function[edit | edit source]

CHRAC1 is a multi-subunit complex that contains the ATPase ISWI, which uses the energy from ATP hydrolysis to alter the structure of chromatin. This remodeling process involves the sliding of nucleosomes along the DNA, which can either increase or decrease the accessibility of the underlying DNA to the transcription machinery.

In addition to ISWI, CHRAC1 also contains several other subunits, including CHRAC-15 and CHRAC-17, which are believed to play a role in targeting the complex to specific regions of the genome. The exact composition of CHRAC1 can vary depending on the cell type and developmental stage, suggesting that different versions of the complex may have distinct functions.

Role in Gene Regulation[edit | edit source]

By modulating the accessibility of chromatin, CHRAC1 plays a key role in the regulation of gene expression. This can have profound effects on a wide range of biological processes, including cell differentiation, development, and response to environmental stimuli.

In particular, CHRAC1 has been implicated in the regulation of genes involved in DNA repair, cell cycle control, and apoptosis. Dysregulation of these processes can lead to a variety of diseases, including cancer.

Clinical Significance[edit | edit source]

Given its role in gene regulation, CHRAC1 has been implicated in a number of diseases, particularly those involving aberrant gene expression. For example, mutations in the ISWI subunit of CHRAC1 have been linked to several types of cancer, including breast cancer and colorectal cancer.

In addition, CHRAC1 has been suggested as a potential therapeutic target for the treatment of certain diseases. For example, drugs that modulate the activity of CHRAC1 could potentially be used to alter the expression of disease-associated genes.

See Also[edit | edit source]

References[edit | edit source]


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Contributors: Prab R. Tumpati, MD