Sieber, Alina; Parr, Marina; Ehr, Julian von; Dhamotharan, Karthikeyan; Kielkowski, Pavel; Brewer, Tess; Schäpers, Anna; Krafczyk, Ralph; Qi, Fei; Schlundt, Andreas; Frishman, Dmitrij; Lassak, Jürgen (2024): EF-P and its paralog EfpL (YeiP) differentially control translation of proline-containing sequences. Nature Communications, 15: 10465. ISSN 2041-1723
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Abstract
Polyproline sequences are deleterious to cells because they stall ribosomes. In bacteria, EF-P plays an important role in overcoming such polyproline sequence-induced ribosome stalling. Additionally, numerous bacteria possess an EF-P paralog called EfpL (also known as YeiP) of unknown function. Here, we functionally and structurally characterize EfpL from Escherichia coli and demonstrate its role in the translational stress response. Through ribosome profiling, we analyze the EfpL arrest motif spectrum and find additional sequences beyond the canonical polyproline motifs that both EF-P and EfpL can resolve. Notably, the two factors can also induce pauses. We further report that EfpL can sense the metabolic state of the cell via lysine acylation. Overall, our work characterizes the role of EfpL in ribosome rescue at proline-containing sequences, and provides evidence that co-occurrence of EF-P and EfpL is an evolutionary driver for higher bacterial growth rates.
Doc-Type: | Article (LMU) |
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Organisational unit (Faculties): | 19 Biology |
DFG subject classification of scientific disciplines: | Life sciences |
Date Deposited: | 05. May 2025 09:05 |
Last Modified: | 06. May 2025 10:27 |
URI: | https://oa-fund.ub.uni-muenchen.de/id/eprint/1839 |
DFG: | Funded by the Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) - 491502892 |