Mitochondrial ribosomal protein L15

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Mitochondrial ribosomal protein L15 (MRPL15) is a protein that in humans is encoded by the MRPL15 gene. This protein is a component of the mitochondrial ribosome, which is specialized for the synthesis of mitochondrial proteins. The mitochondrial ribosome is distinct from the cytoplasmic ribosomes of the cell, and MRPL15 plays a critical role in the function of the mitochondrial ribosome, particularly in the assembly and stability of the large ribosomal subunit.

Function[edit | edit source]

Mitochondrial ribosomal proteins (MRPs) are essential for mitochondrial DNA-encoded protein synthesis within the mitochondrion. MRPL15 is part of the large ribosomal subunit and contributes to the synthesis of mitochondrial proteins, which are crucial for the mitochondrion's role in energy production. The mitochondrion is often referred to as the powerhouse of the cell, and the proteins synthesized by the mitochondrial ribosome are integral to the electron transport chain and ATP synthesis.

Gene[edit | edit source]

The MRPL15 gene is located on the chromosome 3 in humans. It consists of multiple exons and introns that encode the MRPL15 protein. The regulation of this gene is crucial for the proper synthesis of mitochondrial proteins and, consequently, for mitochondrial function.

Structure[edit | edit source]

MRPL15 is a component of the 39S large subunit of the mitochondrial ribosome. Its structure, like that of other mitochondrial ribosomal proteins, is adapted to function within the mitochondrion. The exact structure of MRPL15 and how it interacts with other components of the mitochondrial ribosome to facilitate protein synthesis is an area of ongoing research.

Clinical Significance[edit | edit source]

Alterations in the MRPL15 gene can lead to mitochondrial dysfunction, which is associated with a variety of diseases and conditions. Given the critical role of mitochondria in energy production, defects in mitochondrial protein synthesis can lead to diseases characterized by energy deficiency. However, the specific diseases associated with mutations in the MRPL15 gene are not well-defined, highlighting the need for further research in this area.

See Also[edit | edit source]

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Contributors: Prab R. Tumpati, MD