Evidence map›Paper›PMID 29052983›Full record

ArticleBiochemistry2018

In Vivo Biochemistry: Single-Cell Dynamics of Cyclic Di-GMP in Escherichia coli in Response to Zinc Overload.

Jongchan Yeo, Andrew B Dippel, Xin C Wang, Ming C Hammond

Abstract read
In one paragraph

Article in Biochemistry, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

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  14. "Second-generation" fluorogenic RNA-based sensors.Methods (San Diego, Calif.) · 2019
    Review
  15. Article
  16. Review
  17. Live Flow Cytometry Analysis of c-di-GMP Levels in Single Cell Populations.Methods in molecular biology (Clifton, N.J.) · 2017
    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

4 authors at 1 institution in 1 country.

Jongchan YeoDepartment of Chemistry, University of California , Berkeley, California 94720, United States.
Andrew B DippelDepartment of Chemistry, University of California , Berkeley, California 94720, United States.
Xin C WangDepartment of Molecular & Cell Biology, University of California , Berkeley, California 94720, United States.
Ming C HammondDepartment of Chemistry, University of California , Berkeley, California 94720, United States.ORCID 0000-0003-2666-4764
University of California, Berkeley · US

Funding

Enabling High-Throughput Analysis and Single-Cell Imaging of Bacterial SignalsR01GM124589 · NIGMS · UTAH STATE HIGHER EDUCATION SYSTEM--UNIVERSITY OF UTAH · PI HAMMOND, MING CHEN · 2017 to 2025
$2.8M
A Chemical Biology Approach to Tagging RNAs in Live CellsDP2OD008677 · OD · UNIVERSITY OF CALIFORNIA BERKELEY · PI HAMMOND, MING CHEN · 2011 to 2011
$2.3M
NIGMS NIH HHS R01 GM124589NIH HHS DP2 OD008677
6 · The paper itself

Abstract

Intracellular signaling enzymes drive critical changes in cellular physiology and gene expression, but their endogenous activities in vivo remain highly challenging to study in real time and for individual cells. Here we show that flow cytometry can be performed in complex media to monitor single-cell population distributions and dynamics of cyclic di-GMP signaling, which controls the bacterial colonization program. These in vivo biochemistry experiments are enabled by our second-generation RNA-based fluorescent (RBF) biosensors, which exhibit high fluorescence turn-on in response to cyclic di-GMP. Specifically, we demonstrate that intracellular levels of cyclic di-GMP in Escherichia coli are repressed with excess zinc, but not with other divalent metals. Furthermore, in both flow cytometry and fluorescence microscopy setups, we monitor the dynamic increase in cellular cyclic di-GMP levels upon zinc depletion and show that this response is due to de-repression of the endogenous diguanylate cyclase DgcZ. In the presence of zinc, cells exhibit enhanced cell motility and increased sensitivity to antibiotics due to inhibited biofilm formation. Taken together, these results showcase the application of RBF biosensors in visualizing single-cell dynamic changes in cyclic di-GMP signaling in direct response to environmental cues such as zinc and highlight our ability to assess whether observed phenotypes are related to specific signaling enzymes and pathways.

Indexed as

Biosensing TechniquesSingle-Cell AnalysisCyclic GMPEscherichia coliFlow CytometryMicroscopy, FluorescenceRNASignal TransductionZincbis(3',5')-cyclic diguanylic acidCyclic GMPRNAZinc

Identifiers

PMID29052983
PMCPMC5942897
OpenAlexW2766467561

What OpenQuestion holds

Textmetadata
LicenceTDM
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.