CSRP3: Difference between revisions

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[[Category:Cardiomyopathy]]
[[Category:Cardiomyopathy]]
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Latest revision as of 05:57, 17 March 2025


Overview[edit]

CSRP3 (Cysteine and Glycine-Rich Protein 3) is a protein encoded by the CSRP3 gene in humans. It is a member of the LIM domain protein family, which is characterized by the presence of LIM domains that are involved in protein-protein interactions. CSRP3 is also known as Muscle LIM Protein (MLP) and plays a crucial role in muscle development and function.

Structure[edit]

CSRP3 contains two LIM domains, which are zinc finger-like motifs that facilitate interactions with other proteins. These domains are essential for the protein's role in muscle cell differentiation and maintenance. The protein is predominantly expressed in cardiac and skeletal muscle tissues.

Function[edit]

CSRP3 is involved in the regulation of muscle cell differentiation and growth. It acts as a scaffold protein, interacting with other proteins to form complexes that are critical for muscle function. CSRP3 is also implicated in the mechanotransduction pathways, which are processes by which cells convert mechanical stimuli into chemical activity.

Clinical Significance[edit]

Mutations in the CSRP3 gene have been associated with various cardiomyopathies, including hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM). These conditions are characterized by abnormal heart muscle structure and function, leading to heart failure and other complications.

Research[edit]

Ongoing research is focused on understanding the precise molecular mechanisms by which CSRP3 mutations lead to cardiomyopathy. Studies are also exploring potential therapeutic strategies to target these pathways and ameliorate the effects of these mutations.

Also see[edit]

References[edit]

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