Chromosome 12 Open Reading Frame 65 (C12orf65)

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Chromosome 12 Open Reading Frame 65 (C12orf65)
Mitochondrial DNA encodes 13 proteins of oxidative phosphorylation, and these are translated on dedicated mitochondrial ribosomes with translation machinery that resembles that of prokaryotes. C12ORF65 encodes a protein that is critical for the release of newly synthesized proteins from mitochondrial ribosomes. C12ORF65-mutant fibroblasts cultured from 2 patients with a combined oxidative phosphorylation deficiency (COXPD7) showed global and uniform defect in translation of mitochondrial DNA-encoded proteins, resulting in a severe decrease of oxidative phosphorylation complexes I, IV, and V, and a small decrease in complex III. Expression of wildtype C12ORF65 rescued the defect, and overexpression of the mitochondrial release factor ICT1 partly rescued the defect, suggesting C12ORF65 may have a role in releasing peptides from mitochondrial ribosomes.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Chromosome 12 Open Reading Frame 65 (C12orf65) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Chromosome 12 Open Reading Frame 65 (C12orf65) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Chromosome 12 Open Reading Frame 65 (C12orf65) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Chromosome 12 Open Reading Frame 65 (C12orf65) CLIA Kit Customized Service Offer
n/a ELISA Kit for Chromosome 12 Open Reading Frame 65 (C12orf65) ELISA Kit Customized Service Offer
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  2. "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
  3. "Mutations in C12orf65 in patients with encephalomyopathy and a mitochondrial translation defect."Am. J. Hum. Genet. 87:115-122(2010) [PubMed] [Europe PMC] [Abstract]
  4. "A functional peptidyl-tRNA hydrolase, ICT1, has been recruited into the human mitochondrial ribosome."EMBO J. 29:1116-1125(2010) [PubMed] [Europe PMC] [Abstract]
  5. "A homozygous mutation of C12orf65 causes spastic paraplegia with optic atrophy and neuropathy (SPG55)."J. Med. Genet. 49:777-784(2012) [PubMed] [Europe PMC] [Abstract]
  6. "Solution structure and siRNA-mediated knockdown analysis of the mitochondrial disease-related protein C12orf65."Proteins 80:2629-2642(2012) [PubMed] [Europe PMC] [Abstract]