Affinage mechanistic annotation for ATP5MJ (human) Affinage Affinage (Claude Sonnet reading pass + Opus synthesis pass) 3 citations

Affinage mechanistic annotation for ATP5MJ (human)

Current model (mechanistic narrative)

ATP5MJ (MLQ/6.8PL) encodes a small mitochondrial proteolipid that post-transcriptionally controls the abundance of the ATP synthase complex PMID:24330338. Its knockdown reduces the mitochondrial population of ATP synthase without altering the mRNA levels of ATP synthase α- and β-subunits, and lowers mitochondrial ATP synthesis activity, slows cell growth, and sensitizes cells to glucose deprivation, establishing it as a determinant of assembled ATP synthase levels rather than a transcriptional regulator PMID:24330338. The ATP5MJ 3' UTR harbors a functional SECIS element that binds SECISBP2 and supports UGA readthrough for selenocysteine insertion, linking the transcript to selenoprotein synthesis machinery PMID:41201471. Beyond these observations, the structural basis of its association with ATP synthase and its mechanism of action have not been characterized in the available corpus.

Affinage mechanism profile (Affinage's own GO/Reactome grounding)

Dated findings (citation-anchored)

Year Confidence Finding PMIDs Journal
2013 Medium MLQ (ATP5MJ/6.8PL) knockdown in HeLa cells reduces the population of ATP synthase in mitochondria without affecting mRNA levels of ATP synthase α- and β-subunits, indicating that MLQ controls ATP synthase abundance post-transcriptionally. Knockdown cells show decreased mitochondrial ATP synthesis activity, slower growth, and increased vulnerability to glucose deprivation. PMID:24330338 Genes to cells : devoted to molecular & cellular mechanisms
2014 Low The 6.8 kDa mitochondrial proteolipid MLQ (ATP5MJ) was identified as differentially expressed in mitochondria isolated from peripheral blood mononuclear cells of type 2 diabetic patients compared to healthy controls, placing it among ATP synthase-related proteins altered in disease. PMID:25420343 European journal of mass spectrometry (Chichester, England)
2025 Medium The 3' UTR of ATP5MJ mRNA contains a functional SECIS (selenocysteine insertion sequence) element, as validated by luciferase assays and fusion to known selenoprotein RNAs, indicating that ATP5MJ transcripts can support UGA stop codon readthrough for selenocysteine insertion. PMID:41201471 Redox biology

Citations