MT-TE: Difference between revisions
CSV import |
CSV import |
||
| Line 25: | Line 25: | ||
{{medicine-stub}} | {{medicine-stub}} | ||
{{No image}} | {{No image}} | ||
__NOINDEX__ | |||
Latest revision as of 12:23, 17 March 2025
MT-TE or Mitochondrial tRNA Threonine is a gene that in humans is encoded by the MT-TE genetic sequence. This gene is a member of the mitochondrial DNA (mtDNA) tRNA family and plays a crucial role in the protein synthesis within the mitochondria.
Function[edit]
The MT-TE gene provides instructions for making a molecule called transfer RNA (tRNA) which is essential for assembling amino acids into functioning proteins. Specifically, the MT-TE gene produces a tRNA molecule that helps incorporate the amino acid threonine into proteins. This process is a critical part of the mitochondrial protein synthesis.
Clinical significance[edit]
Mutations in the MT-TE gene have been associated with several mitochondrial disorders, including Mitochondrial encephalomyopathy, lactic acidosis, and stroke-like episodes (MELAS) and Myoclonic Epilepsy with Ragged Red Fibers (MERRF). These conditions often involve muscle weakness and pain, seizures, and problems with movement and balance.
See also[edit]
References[edit]
<references />
