10 sources retrieved · Most recent: April 2026 · Index updated 14 days ago
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40PubMed Papers
20Diseases
0Drugs
0Pathogenic Variants
DATA QUALITY✓ Experimental GO Evidence✓ Swiss-Prot Reviewed
ribosome disassemblyprotein bindingmitochondrionribosomal large subunit bindingneurodegenerative diseaseocular hypotensiondeficiency anemiamyoepithelial tumor
MRRF (mitochondrial ribosome recycling factor) is a mitochondrial protein responsible for disassembling ribosomes from messenger RNA at the termination of mitochondrial protein biosynthesis 1. The protein functions collaboratively with GFM2 to promote mitochondrial ribosome recycling by dissolving intersubunit contacts between ribosomal subunits 2. This recycling process is essential for completing the translational cycle and releasing ribosomal components for subsequent rounds of protein synthesis. MRRF operates within the mitochondrial matrix and exhibits protein-binding capacity, binding to ribosomal large subunits during the disassembly process 2. The gene exhibits time-dependent expression patterns in response to cellular signals, as demonstrated in LPA-treated human fibroblasts where MRRF expression showed a characteristic up-and-down profile 3. While insufficient information is provided regarding direct disease associations or clinical significance in the available abstracts, the critical role of MRRF in terminating mitochondrial translation suggests its dysfunction could potentially impair mitochondrial protein synthesis and cellular energy metabolism.
1
MRRF is responsible for disassembly of ribosomes from mRNA at termination of mitochondrial protein biosynthesis
PMID: 197167932
MRRF acts in collaboration with GFM2 and promotes mitochondrial ribosome recycling by dissolution of intersubunit contacts
PMID: 338782943
MRRF gene expression shows time-dependent up-and-down profile in response to LPA treatment in human diploid fibroblasts
PMID: 19563823⚠Limited data available — This gene has 3 indexed publications. Summary and analysis may be incomplete.
neurodegenerative diseaseOpen Targets
ocular hypotensionOpen Targets
deficiency anemiaOpen Targets
myoepithelial tumorOpen Targets
lysosomal lipid storage disorderOpen Targets
squamous cell lung carcinomaOpen Targets
alcohol drinkingOpen Targets
mathematical abilityOpen Targets
hypopituitarismOpen Targets
schizophreniaOpen Targets
pyridoxine-dependent epilepsy caused by ALDH7A1 mutantOpen Targets
Parkinson diseaseOpen Targets
psychiatric disorderOpen Targets
No pathogenic variants reported on ClinVar for this gene.