Evidence map›Paper›PMID 19917103›Full record

ArticleBMC systems biology2009

Network analysis of the transcriptional pattern of young and old cells of Escherichia coli during lag phase.

Carmen Pin, Matthew D Rolfe, Marina Muñoz-Cuevas, Jay C D Hinton, Michael W Peck, Nicholas J Walton, József Baranyi

Open access · diamondAbstract read
In one paragraph

Article in BMC systems biology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
2.0field-weighted citation impact, top 13% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 33 citations in OpenAlex.

  1. Regulation of phosphate starvation-specific responses inMicrobiology (Reading, England) · 2023
    Review
  2. Nontraditional systems in aging research: an update.Cellular and molecular life sciences : CMLS · 2021
    Review
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  13. Bacterial aging: from mechanistic basis to evolutionary perspective.Cellular and molecular life sciences : CMLS · 2010
    Review
  14. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 2 countries.

Carmen PinInstitute of Food Research, Norwich NR4 7UA, UK. carmen.pin@bbsrc.ac.uk
Matthew D Rolfe
Marina Muñoz-Cuevas
Jay C D Hinton
Michael W Peck
Nicholas J Walton
József Baranyi
Quadram Institute · GB

Funding

Biotechnology and Biological Sciences Research Council 42230ABiotechnology and Biological Sciences Research Council 42266ABiotechnology and Biological Sciences Research Council BBS/E/F/00042266
6 · The paper itself

Abstract

backgroundThe aging process of bacteria in stationary phase is halted if cells are subcultured and enter lag phase and it is then followed by cellular division. Network science has been applied to analyse the transcriptional response, during lag phase, of bacterial cells starved previously in stationary phase for 1 day (young cells) and 16 days (old cells).

resultsA genome scale network was constructed for E. coli K-12 by connecting genes with operons, transcription and sigma factors, metabolic pathways and cell functional categories. Most of the transcriptional changes were detected immediately upon entering lag phase and were maintained throughout this period. The lag period was longer for older cells and the analysis of the transcriptome revealed different intracellular activity in young and old cells. The number of genes differentially expressed was smaller in old cells (186) than in young cells (467). Relatively, few genes (62) were up- or down-regulated in both cultures. Transcription of genes related to osmotolerance, acid resistance, oxidative stress and adaptation to other stresses was down-regulated in both young and old cells. Regarding carbohydrate metabolism, genes related to the citrate cycle were up-regulated in young cells while old cells up-regulated the Entner Doudoroff and gluconate pathways and down-regulated the pentose phosphate pathway. In both old and young cells, anaerobic respiration and fermentation pathways were down-regulated, but only young cells up-regulated aerobic respiration while there was no evidence of aerobic respiration in old cells.Numerous genes related to DNA maintenance and replication, translation, ribosomal biosynthesis and RNA processing as well as biosynthesis of the cell envelope and flagellum and several components of the chemotaxis signal transduction complex were up-regulated only in young cells. The genes for several transport proteins for iron compounds were up-regulated in both young and old cells. Numerous genes encoding transporters for carbohydrates and organic alcohols and acids were down-regulated in old cells only.

conclusionNetwork analysis revealed very different transcriptional activities during the lag period in old and young cells. Rejuvenation seems to take place during exponential growth by replicative dilution of old cellular components.

Indexed as

Age FactorsCarbohydrate MetabolismCell CycleEscherichia coliGene Expression Regulation, BacterialGene Regulatory NetworksOligonucleotide Array Sequence AnalysisOxidative StressStress, PhysiologicalTranscription FactorsTranscription, GeneticVesicular Transport ProteinsTranscription FactorsVesicular Transport Proteins

Identifiers

PMID19917103
PMCPMC2780417
OpenAlexW2148975232

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.