# MTO1

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**Protein MTO1 homolog, mitochondrial** is a [protein](/source/Protein) that in humans is encoded by the *MTO1* [gene](/source/Gene).[1][2]

## References

1. Li X, Li R, Lin X, Guan MX (Jul 2002). "Isolation and characterization of the putative nuclear modifier gene MTO1 involved in the pathogenesis of deafness-associated mitochondrial 12 S rRNA A1555G mutation". *J Biol Chem*. **277** (30): 27256–64. [doi:10.1074/jbc.M203267200](https://doi.org/10.1074/jbc.M203267200). [PMID 12011058](https://pubmed.ncbi.nlm.nih.gov/12011058)

1. ["Entrez Gene: MTO1 mitochondrial translation optimization 1 homolog (S. cerevisiae)"](https://www.ncbi.nlm.nih.gov/gene?Db=gene&Cmd=ShowDetailView&TermToSearch=25821)

## Further reading

- Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides.". *Gene*. **138** (1–2): 171–4. [doi:10.1016/0378-1119(94)90802-8](https://doi.org/10.1016/0378-1119(94)90802-8). [PMID 8125298](https://pubmed.ncbi.nlm.nih.gov/8125298)
- Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, etal (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". *Gene*. **200** (1–2): 149–56. [doi:10.1016/S0378-1119(97)00411-3](https://doi.org/10.1016/S0378-1119(97)00411-3). [PMID 9373149](https://pubmed.ncbi.nlm.nih.gov/9373149)
- Lai CH, Chou CY, Ch'ang LY, etal (2000). "Identification of novel human genes evolutionarily conserved in Caenorhabditis elegans by comparative proteomics". *Genome Res.*. **10** (5): 703–13. [doi:10.1101/gr.10.5.703](https://doi.org/10.1101/gr.10.5.703). [PMC 310876](https://www.ncbi.nlm.nih.gov/pmc/articles/PMC310876). [PMID 10810093](https://pubmed.ncbi.nlm.nih.gov/10810093)
- Strausberg RL, Feingold EA, Grouse LH, etal (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". *Proc. Natl. Acad. Sci. U.S.A.*. **99** (26): 16899–903. [Bibcode:2002PNAS...9916899M](https://ui.adsabs.harvard.edu/abs/2002PNAS...9916899M). [doi:10.1073/pnas.242603899](https://doi.org/10.1073/pnas.242603899). [PMC 139241](https://www.ncbi.nlm.nih.gov/pmc/articles/PMC139241). [PMID 12477932](https://pubmed.ncbi.nlm.nih.gov/12477932)
- Mungall AJ, Palmer SA, Sims SK, etal (2003). "The DNA sequence and analysis of human chromosome 6". *Nature*. **425** (6960): 805–11. [Bibcode:2003Natur.425..805M](https://ui.adsabs.harvard.edu/abs/2003Natur.425..805M). [doi:10.1038/nature02055](https://doi.org/10.1038/nature02055). [PMID 14574404](https://pubmed.ncbi.nlm.nih.gov/14574404)
- Gerhard DS, Wagner L, Feingold EA, etal (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". *Genome Res.*. **14** (10B): 2121–7. [doi:10.1101/gr.2596504](https://doi.org/10.1101/gr.2596504). [PMC 528928](https://www.ncbi.nlm.nih.gov/pmc/articles/PMC528928). [PMID 15489334](https://pubmed.ncbi.nlm.nih.gov/15489334)
- Bykhovskaya Y, Mengesha E, Wang D, etal (2005). "Phenotype of non-syndromic deafness associated with the mitochondrial A1555G mutation is modulated by mitochondrial RNA modifying enzymes MTO1 and GTPBP3". *Mol. Genet. Metab.*. **83** (3): 199–206. [doi:10.1016/j.ymgme.2004.07.009](https://doi.org/10.1016/j.ymgme.2004.07.009). [PMID 15542390](https://pubmed.ncbi.nlm.nih.gov/15542390)
- Krull M, Brosius J, Schmitz J (2005). "Alu-SINE exonization: en route to protein-coding function". *Mol. Biol. Evol.*. **22** (8): 1702–11. [doi:10.1093/molbev/msi164](https://doi.org/10.1093/molbev/msi164). [PMID 15901843](https://pubmed.ncbi.nlm.nih.gov/15901843)

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