Transfer RNA is highly unstable during early amino acid starvation in Escherichia coli

© The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research..

Due to its long half-life compared to messenger RNA, bacterial transfer RNA is known as stable RNA. Here, we show that tRNAs become highly unstable as part of Escherichia coli's response to amino acid starvation. Degradation of the majority of cellular tRNA occurs within twenty minutes of the onset of starvation for each of several amino acids. Both the non-cognate and cognate tRNA for the amino acid that the cell is starving for are degraded, and both charged and uncharged tRNA species are affected. The alarmone ppGpp orchestrates the stringent response to amino acid starvation. However, tRNA degradation occurs in a ppGpp-independent manner, as it occurs with similar kinetics in a relaxed mutant. Further, we also observe rapid tRNA degradation in response to rifampicin treatment, which does not induce the stringent response. We propose a unifying model for these observations, in which the surplus tRNA is degraded whenever the demand for protein synthesis is reduced. Thus, the tRNA pool is a highly regulated, dynamic entity. We propose that degradation of surplus tRNA could function to reduce mistranslation in the stressed cell, because it would reduce competition between cognate and near-cognate charged tRNAs at the ribosomal A-site.

Medienart:

E-Artikel

Erscheinungsjahr:

2017

Erschienen:

2017

Enthalten in:

Zur Gesamtaufnahme - volume:45

Enthalten in:

Nucleic acids research - 45(2017), 2 vom: 25. Jan., Seite 793-804

Sprache:

Englisch

Beteiligte Personen:

Svenningsen, Sine Lo [VerfasserIn]
Kongstad, Mette [VerfasserIn]
Stenum, Thomas Søndergaard [VerfasserIn]
Muñoz-Gómez, Ana J [VerfasserIn]
Sørensen, Michael A [VerfasserIn]

Links:

Volltext

Themen:

9014-25-9
Amino Acids
Journal Article
RNA, Messenger
RNA, Transfer

Anmerkungen:

Date Completed 06.06.2017

Date Revised 24.03.2024

published: Print-Electronic

Citation Status MEDLINE

doi:

10.1093/nar/gkw1169

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM266700624