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Published on: May 23, 2021
Characterization of YjjJ toxin of Escherichia coli
Yuki Maeda1, Chun-Yi Lin2, Yojiro Ishida2
1Department of Biology, Graduate School of Science, Osaka City University, Sumiyoshi-ku, Osaka 558-8585, Japan.
Abstract:
Reminiscent of eukaryotic apoptotic programmed cell death, bacteria also contain a large number of suicide genes, which are in general co-expressed with their cognate antitoxin genes. These systems called the toxin-antitoxin (TA) systems are associated with cellular dormancy, and play major roles in biofilm formation and persistent multidrug resistance of many human pathogens. In recent years, the study on TA system toxins has become a hot topic due to the health implications of these toxins by virtue of their role in bacterial pathogenicity. Here we report functional characterization of a hitherto uncharacterized Escherichia coli TA toxin, YjjJ. YjjJ exhibits several uncommon properties: (i) unlike the genes encoding most type II TA system toxins, the gene encoding YjjJ is present as a single gene and not in an operon, (ii) despite being a homolog of the well-characterized toxin HipA, YjjJ seems to have different cellular target(s), and (iii) HipB, the cognate antitoxin of HipA, also acts as an antitoxin for YjjJ. This forms a basis for an interesting next step in the study of TA systems with respect to cross-regulation between various TA systems and the evolutionary as well as clinical significance of these observations.
Insights
Bacteria utilize toxin-antitoxin (TA) systems for dormancy and drug resistance. This study characterizes YjjJ, an Escherichia coli TA toxin with unique properties, including shared antitoxin regulation, impacting bacterial pathogenicity.
Area of Science:
- Microbiology
- Molecular Biology
- Bacterial Pathogenesis
Background:
- Bacterial toxin-antitoxin (TA) systems are analogous to eukaryotic programmed cell death.
- TA systems are crucial for bacterial dormancy, biofilm formation, and multidrug resistance.
- The pathogenicity roles of TA system toxins make them a significant research focus.
Purpose of the Study:
- To functionally characterize the previously unstudied Escherichia coli toxin, YjjJ.
- To investigate the unique properties of YjjJ within the context of type II TA systems.
- To explore potential cross-regulation between different TA systems.
Main Methods:
- Functional characterization of the YjjJ toxin from Escherichia coli.
- Comparative analysis with the well-characterized HipA toxin and its antitoxin HipB.
- Investigation of gene organization and antitoxin specificity.
Main Results:
- YjjJ is encoded as a single gene, differing from typical operon structures of type II TA toxins.
- YjjJ, despite being a HipA homolog, appears to target different cellular components.
- HipB, the antitoxin for HipA, also functions as an antitoxin for YjjJ.
Conclusions:
- YjjJ possesses unique characteristics, including its gene structure and antitoxin interaction.
- The shared antitoxin HipB suggests cross-regulation between different TA systems.
- These findings have implications for understanding TA system evolution and clinical relevance in bacterial pathogens.
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