Data · dataset · 2015
The multicopy sRNA LhrC controls expression of the oligopeptide-binding protein OppA in Listeria monocytogenes
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Listeria monocytogenes is the causative agent of the foodborne disease listeriosis.
Description
During infection, L. monocytogenes produces an array of non-coding RNAs, including the multicopy sRNA LhrC. These five, nearly identical sRNAs are highly induced in response to cell envelope stress and target the virulence adhesin lapB at the post-transcriptional level.
Here, we demonstrate that LhrC controls expression of additional genes encoding cell envelope-associated proteins with virulence function. Using transcriptomics and proteomics, we identified a set of genes affected by LhrC in response to cell envelope stress. Three targets were significantly down-regulated by LhrC at both the RNA and protein level: lmo2349, tcsA and oppA .
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All three genes encode membrane-associated proteins: A putative substrate binding protein of an amino acid ABC transporter (Lmo2349); the CD4+ T cell-stimulating antigen TcsA, and the oligopeptide binding protein OppA, of which the latter two are required for full virulence of L. monocytogenes . For OppA, we show that LhrC acts by direct base paring to the ribosome binding site of the oppA mRNA, leading to an impediment of its translation and a decreased mRNA level.
The sRNA-mRNA interaction depends on two of three CU-rich regions in LhrC allowing binding of two oppA mRNAs to a single LhrC molecule. Finally, we found that LhrC contributes to infection in macrophage-like cells. These findings demonstrate a central role for LhrC in controlling the level of OppA and other virulence-associated cell envelope proteins in response to cell envelope stress.
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- Repository landing page tandf.figshare.com/articles/dataset/The_multicopy_sRNA_LhrC_controls_expression_o… ↗
landing page · from DataCite
- DOI doi.org/10.6084/m9.figshare.1483479.v1 ↗
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Documentation and papers
- Creative Commons Attribution 4.0 International creativecommons.org/licenses/by/4.0/legalcode ↗
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- IsSupplementTo 10.1080/15476286.2015.1071011 doi.org/10.1080/15476286.2015.1071011 ↗
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- DataCite API api.datacite.org/dois/10.6084/m9.figshare.1483479.v1 ↗
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- DataCite Commons commons.datacite.org/doi.org/10.6084/m9.figshare.1483479.v1 ↗
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Topics
- Stated by source
- Biological sciences · Clinical medicine · Health sciences
- From keywords
- Biochemistry and cell biology · Cancer · Genetics · Immunology
- Inferred from text
- Disease 75% · Mass spectrometry 65%
Related
Provenance · 1 source records, 14 field assertions
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|---|---|---|---|
| DataCite | 10.6084/m9.figshare.1483479.v1 | 12 d ago | JSON v1 |
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