ArticleNucleic acids research2026
Cleavage of host tRNAs by mycoplasma membrane-associated nuclease.
Article in Nucleic acids research, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
What it found
Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.
The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
Abstract
Mycoplasmas are pathogens causing infectious diseases in various animals, including humans. They are also common contaminants of cell culture. Although it is suggested that mycoplasmas alter nucleic acid metabolism of host cells through their nucleases, the actual impact of the nucleases on host cell RNAs is unknown. Here we report that Mycoplasma hyorhinis, a common laboratory contaminant species, promotes cleavage of host cell transfer RNAs (tRNAs) through a membrane-associated nuclease. When infected by M. hyorhinis, scraping of cells as well as cell lysis induced a marked cleavage of host RNAs. Further analysis suggested that the protein encoded by the membrane nuclease A (mnuA) gene is responsible for the host RNA cleavage. MnuA protein demonstrates DNase and RNase activities dependent on Ca2+/Mg2+ ions. Purified MnuA protein acts as an atypical sugar non-specific nuclease: while it possesses broad DNase activities, its RNase activity is highly specific to tRNAs in live cells. Mutational analysis shows that the nuclease activity is mediated by a domain which is highly similar to DNase I. Furthermore, M. hyorhinis promoted cleavage of host tRNAs under amino acid deprivation, suggesting that M. hyorhinis infection may alter RNA metabolism in host cells under certain physiological stress. As mnuA genes are conserved in various mycoplasma species, our findings provide novel insights into the effects of MnuA nucleases on host cell RNAs under mycoplasma infection.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.