MT-TT: Difference between revisions
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Revision as of 03:33, 11 February 2025
MT-TT is a gene that in humans is encoded by the MT-TT mitochondrial DNA. This gene provides instructions for making a molecule called transfer RNA (tRNA) that is essential for protein production. MT-TT is a small structural RNA molecule component of the mitochondrial ribosome, which is involved in the protein synthesis within the mitochondrion.
Function
The MT-TT gene is located within the mitochondrial genome, which is found in the mitochondria. Mitochondria are structures within cells that convert the energy from food into a form that cells can use. Each cell contains hundreds to thousands of mitochondria, which are located in the fluid that surrounds the nucleus (the cytoplasm).
The MT-TT gene provides instructions for making a molecule called transfer RNA (tRNA), which is essential for protein production. Transfer RNA helps assemble protein building blocks (amino acids) into functioning proteins.
Clinical significance
Mutations in the MT-TT gene have been associated with several mitochondrial disorders, including mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS), myoclonic epilepsy with ragged-red fibers (MERRF), and Leber's hereditary optic neuropathy (LHON). These conditions often involve muscle weakness and pain, seizures, vision loss, and abnormalities of the heart, liver, and kidneys.
See also
References
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