Understanding bacterial epitranscriptomics on the basis of Escherichia coli – T4 phage interactions
The principal knowledge gap in T4 phage biology is linked to the importance of identifying the molecular mechanisms by which viruses hijack their host’s genetic machinery at the transcriptional and translational level.
In this project, we characterise the bacterial epitranscriptome on the basis of T4 phage – E. coli interaction. By combining next-generation sequencing strategies and proteomic approaches, we will study the molecular influence of post-translational protein modifications such as ADP-ribosylation and RNAylation on the central cellular processes of transcription and translation during phage-host interactions. This study will broaden our understanding of how the ADP-ribosyltransferases of the T4 phage modulate the bacterial key mechanisms and inhibit bacterial defence mechanisms to trigger an effective infection.
Figure 1: ADP-ribosylation and RNAylation of target proteins by T4 phage ADP-ribosyltransferase ModB. ModB accepts NAD as well as NAD-capped-RNA as substrate, thereby covalently linking ADP-ribose (ADP-ribosylation) or ADP-ribose modified-RNA (RNAylation) to a target protein.
Dr. Katharina Höfer Max-Planck-Institute for Terrestrial Microbiology Karl-von-Frisch-Str. 16 35043 Marburg, Germany
Höfer K*, Schauerte M, Grawenhoff J, Wulf A, Welp LM, Billau FA, Urlaub H, Jäschke A* (2021) Viral ADP-ribosyltransferases attach RNA chains to host proteins. bioRxiv, doi: https://doi.org/10.1101/2021.06.04.446905
Schauerte M, Pozhydaieva N, Höfer K* (2021) Shaping the Bacterial Epitranscriptome—5′-Terminal and Internal RNA Modifications. Advanced Biology, doi: https://doi.org/10.1002/adbi.202100834