Serum response factor

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Serum response factor (SRF) is a transcription factor that binds to the serum response element (SRE), a short sequence of DNA found in the promoter region of some genes. It is a crucial component of the cellular machinery that regulates gene expression. SRF is involved in a wide range of physiological processes, including cell growth and differentiation, muscle development, and the response to serum stimulation.

Structure[edit | edit source]

SRF is a member of the MADS (MCM1, Agamous, Deficiens, and SRF) box superfamily of transcription factors. It contains a highly conserved DNA-binding domain, known as the MADS box, which allows it to bind to the SRE in the promoter region of target genes. The MADS box is approximately 58 amino acids in length and is located towards the N-terminus of the protein.

Function[edit | edit source]

SRF regulates the expression of a large number of genes that are involved in a variety of cellular processes. These include genes that encode proteins involved in cell cycle regulation, cytoskeletal organization, and muscle differentiation. SRF can either activate or repress the transcription of these genes, depending on the context.

In response to serum stimulation, SRF binds to the SRE in the promoter region of immediate early genes, such as c-fos, and activates their transcription. This is a crucial step in the cellular response to growth signals.

In muscle cells, SRF plays a key role in the regulation of muscle-specific genes. It binds to the SRE in the promoter region of these genes and activates their transcription, leading to muscle differentiation.

Clinical significance[edit | edit source]

Alterations in SRF function have been implicated in a number of diseases, including cancer, cardiovascular disease, and neurodegenerative disease. In cancer, overexpression of SRF has been observed in several types of tumors, and it has been suggested that SRF may contribute to tumor growth and progression. In cardiovascular disease, mutations in SRF have been linked to congenital heart defects and cardiomyopathy. In neurodegenerative disease, changes in SRF activity have been associated with Alzheimer's disease and Parkinson's disease.

See also[edit | edit source]


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Contributors: Prab R. Tumpati, MD