40S ribosomal protein S14

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Ideogram human chromosome 5.svg

40S ribosomal protein S14 is a protein that in humans is encoded by the RPS14 gene. This protein is a component of the 40S subunit of the ribosome, which is involved in the initiation of protein synthesis. The 40S ribosomal proteins play a key role in the molecular mechanisms that regulate gene expression, cell growth, and cell division.

Function[edit | edit source]

The 40S ribosomal protein S14 is integral to the function of the ribosomes, which are essential for protein synthesis within the cell. Ribosomes translate messenger RNA (mRNA) sequences into amino acid chains, which then fold into functional proteins. The 40S subunit, in particular, is involved in the initiation phase of this process, binding to mRNA and the 60S ribosomal subunit to form the complete 80S ribosome in eukaryotic cells. Protein S14 contributes to the structural integrity of the 40S subunit and plays a role in the recognition and binding of mRNA.

Gene[edit | edit source]

The RPS14 gene is located on chromosome 5 in humans. It encodes the 40S ribosomal protein S14, which is one of the proteins that make up the small subunit of the ribosome. Mutations in the RPS14 gene have been associated with certain genetic disorders and diseases, including Diamond-Blackfan anemia, a rare bone marrow failure syndrome characterized by anemia that usually presents in early childhood.

Clinical Significance[edit | edit source]

Alterations in the expression or function of ribosomal proteins, including S14, can lead to ribosomopathies, a group of disorders caused by defects in ribosome biogenesis or function. These conditions often manifest as specific clinical syndromes, such as Diamond-Blackfan anemia, which is linked to mutations in ribosomal protein genes. Understanding the role of proteins like S14 in ribosome function helps in the diagnosis and treatment of these diseases.

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Contributors: Prab R. Tumpati, MD