A systematic analysis of the RNA-targeting potential of secreted bacterial effector proteins.
Average rating
Cast your vote
You can rate an item by clicking the amount of stars they wish to award to this item.
When enough users have cast their vote on this item, the average rating will also be shown.
Star rating
Your vote was cast
Thank you for your feedback
Thank you for your feedback
Issue Date
2017-08-24
Metadata
Show full item recordAbstract
Many pathogenic bacteria utilize specialized secretion systems to deliver proteins called effectors into eukaryotic cells for manipulation of host pathways. The vast majority of known effector targets are host proteins, whereas a potential targeting of host nucleic acids remains little explored. There is only one family of effectors known to target DNA directly, and effectors binding host RNA are unknown. Here, we take a two-pronged approach to search for RNA-binding effectors, combining biocomputational prediction of RNA-binding domains (RBDs) in a newly assembled comprehensive dataset of bacterial secreted proteins, and experimental screening for RNA binding in mammalian cells. Only a small subset of effectors were predicted to carry an RBD, indicating that if RNA targeting was common, it would likely involve new types of RBDs. Our experimental evaluation of effectors with predicted RBDs further argues for a general paucity of RNA binding activities amongst bacterial effectors. We obtained evidence that PipB2 and Lpg2844, effector proteins of Salmonella and Legionella species, respectively, may harbor novel biochemical activities. Our study presenting the first systematic evaluation of the RNA-targeting potential of bacterial effectors offers a basis for discussion of whether or not host RNA is a prominent target of secreted bacterial proteins.Citation
A systematic analysis of the RNA-targeting potential of secreted bacterial effector proteins. 2017, 7 (1):9328 Sci RepAffiliation
Helmholtz-Institut für RNA-basierte Infektionsforschung, Josef-Schneider-Straße2, 97080 Würzburg, Germany.Journal
Scientific reportsPubMed ID
28839189Type
ArticleLanguage
enISSN
2045-2322ae974a485f413a2113503eed53cd6c53
10.1038/s41598-017-09527-0
Scopus Count
The following license files are associated with this item:
- Creative Commons
Except where otherwise noted, this item's license is described as http://creativecommons.org/licenses/by-nc-sa/4.0/
Related articles
- An acetyltransferase effector conserved across Legionella species targets the eukaryotic eIF3 complex to modulate protein translation.
- Authors: Syriste L, Patel DT, Stogios PJ, Skarina T, Patel D, Savchenko A
- Issue date: 2024 Mar 13
- A new means to identify type 3 secreted effectors: functionally interchangeable class IB chaperones recognize a conserved sequence.
- Authors: Costa SC, Schmitz AM, Jahufar FF, Boyd JD, Cho MY, Glicksman MA, Lesser CF
- Issue date: 2012
- High-Throughput Screening of Type III Secretion Determinants Reveals a Major Chaperone-Independent Pathway.
- Authors: Ernst NH, Reeves AZ, Ramseyer JE, Lesser CF
- Issue date: 2018 Jun 19
- Subcellular targeting of Salmonella virulence proteins by host-mediated S-palmitoylation.
- Authors: Hicks SW, Charron G, Hang HC, Galán JE
- Issue date: 2011 Jul 21
- Screening Legionella effectors for antiviral effects reveals Rab1 GTPase as a proviral factor coopted for tombusvirus replication.
- Authors: Inaba JI, Xu K, Kovalev N, Ramanathan H, Roy CR, Lindenbach BD, Nagy PD
- Issue date: 2019 Oct 22