NucLoc · RNA localization in bacteria
Horizon 2020 — Marie Skłodowska-Curie Actions
- Duration
- 2018-09-01 → 2020-08-31
- EU contribution
- €165,599
- Participants
- 1
- Scheme
- MSCA-IF
Lines connect the coordinator with its partners.
Results in brief
RNA localization in bacteria
In eukaryotic cells mRNAs can be localized to specific places within a cell to achieve protein synthesis with spacial and temporal control. Recently, I and others have shown that bacteria can also target mRNAs to specific regions of the cell. Problem being addressed- Previous mRNA localization studies in bacteria were primarily restricted to a limited number of mRNAs, and due to the serendipitous nature of these discoveries and conflicting results, it is not clear how widespread mRNA localization is in bacterial cells and what conserved mechanisms are playing a role. To investigate this, I will assess the localization of mRNAs coding for different classes of localized proteins in the model bacterium Bacillus subtilis. Overall objectives- 1) To develop single molecule RNA FISH (smFISH) to visualize mRNAs in Bacillus subtilis 2) Develop a novel next generation sequencing based approach to identify all the mRNAs localized at the bacterial membrane 3) To investigate the role of protein translation, genome location and cell morphology on bacterial mRNAs localization This project is designed provide a unique insight into the scale and mechanisms of mRNA localization in bacteria.
Data: CORDIS, © European Union
Project objective
In eukaryotic cells mRNAs can be localized to specific places within a cell to achieve protein synthesis with spatiotemporal control. Recently, I and others have shown that prokaryotes can also target mRNAs to specific parts of the cell. However, these studies have been restricted to a limited number of mRNAs and were performed with Gram-negative bacteria, and due to the serendipitous nature of these discoveries and conflicting results, it is not clear how widespread mRNA localization is in a bacterial cell and what conserved mechanisms are playing a role. To investigate this, I will first employ a novel CLIP-seq-inspired deep-sequencing-based approach to gain an unbiased view of mRNAs enriched at the cell periphery and cell poles of the Gram-positive model bacterium Bacillus subtilis. This dataset will reveal the scope of mRNA targeting by the Signal Recognition Particle (SRP) and will reveal mRNAs that use another mechanism for cellular targeting. In addition, classic CLIP-seq experiments will be used to identify mRNAs that use the cytoskeleton and other morphological proteins for targeting. As a complementary approach, I will assess the localization of mRNAs coding for different classes of localized proteins (polar, cell division, cytoskeletal, membrane, secreted, motility, nucleoid and chaperone proteins) using the established fluorescence in situ hybridization (FISH) technique. Information obtained from these experiments will subsequently be used to investigate the role of protein translation, RNA sequences, genome location and cell morphology in mRNA localization, to gain functional insight into the mechanisms responsible for this basic morphogenetic process.
Original text from CORDIS.
Participants
- UNIVERSITEIT VAN AMSTERDAM · AmsterdamCoordinatorNetherlands
Links
Data: CORDIS, © European Union