Literature DB >> 9504714

RNase E, the major player in mRNA degradation, is down-regulated in Escherichia coli during a transient growth retardation (diauxic lag).

T Barlow1, M Berkmen, D Georgellis, L Bayr, S Arvidson, A von Gabain.   

Abstract

The endoribonuclease RNase E plays a major part in mRNA degradation in Escherichia coli in addition to its role in processing rRNA. RNase E is encoded by an essential gene, rne, also known as ams and hmp, which is autoregulated post-transcriptionally. Here we report a transient decrease in the steady state level of the full-length rne transcript and a corresponding decline in the amount of the protein and enzymatic activity. During this period an mRNA fragment, lacking an intact 5' end, accumulates. This down-regulation of RNase E occurs under aerobic growth conditions in rich medium during a short diauxic lag in mid-exponential phase; it most likely reflects an exhaustion of a not yet identified medium compound which is followed by switching on a new metabolic pathway. During this lag, the levels of bulk protein are maintained. Our results suggest that a transient drop in the intracellular RNase E level is a means of cells to retard mRNA turnover in a period of adjustment to medium utilization. Furthermore, the here described regulation of the rne transcript and its cognate gene product seems to occur by an RNase E-independent mechanism responsive to changes in growth conditions.

Entities:  

Mesh:

Substances:

Year:  1998        PMID: 9504714     DOI: 10.1515/bchm.1998.379.1.33

Source DB:  PubMed          Journal:  Biol Chem        ISSN: 1431-6730            Impact factor:   3.915


  2 in total

Review 1.  mRNA decay in Escherichia coli comes of age.

Authors:  Sidney R Kushner
Journal:  J Bacteriol       Date:  2002-09       Impact factor: 3.490

Review 2.  Metabolic alarms and cell division in Escherichia coli.

Authors:  D Joseleau-Petit; D Vinella; R D'Ari
Journal:  J Bacteriol       Date:  1999-01       Impact factor: 3.490

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.