Evidence map›Paper›PMID 31406376›Full record

ArticleNature chemical biology2019

Inducible asymmetric cell division and cell differentiation in a bacterium.

Nikolai V Mushnikov, Anastasia Fomicheva, Mark Gomelsky, Grant R Bowman

Open access · greenAbstract read
In one paragraph

Article in Nature chemical biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
4.1field-weighted citation impact, top 6% 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

23 citing papers in PubMed, 46 citations in OpenAlex.

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  11. You're in then you're out.Nature chemical biology · 2023
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  18. Proceedings of the 7th ACM International Conference on Nanoscale Computing and Communication : Virtual Conference, September 23-25, 2020 : NanoCom 2020. ACM International Conference on Nanoscale Computing and Communication (7th : 2020 :... · 2020
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Nikolai V MushnikovDepartment of Molecular Biology, University of Wyoming, Laramie, WY, USA.ORCID http://orcid.org/0000-0002-2429-3624
Anastasia FomichevaDepartment of Molecular Biology, University of Wyoming, Laramie, WY, USA.
Mark GomelskyDepartment of Molecular Biology, University of Wyoming, Laramie, WY, USA.
Grant R BowmanDepartment of Molecular Biology, University of Wyoming, Laramie, WY, USA. grant.bowman@uwyo.edu.ORCID http://orcid.org/0000-0002-8817-8262
University of Wyoming · US

Funding

University of Colorado Cancer Center Support Grant - Lung Cancer Patient-Derived Xenografts with Autologous Human Immune SystemsP30CA046934 · NCI · UNIVERSITY OF COLORADO DENVER · PI James V Degregori · 1988 to 2026
$117.0M
Wyoming INBRE Phase 4- Equipment Supplement for x-ray diffractometer for Center for Advanced Scientific InstrumentationP20GM103432 · NIGMS · UNIVERSITY OF WYOMING · PI Robert Scott Seville · 2012 to 2026
$56.8M
Bacterial Mechanisms for Establishing and Maintaining Cell PolarityR01GM118792 · NIGMS · UNIVERSITY OF WYOMING · PI BOWMAN, GRANT ROBERT · 2016 to 2019
$821k
NCI NIH HHS P30 CA046934NIGMS NIH HHS P20 GM103432NIGMS NIH HHS R01 GM118792
6 · The paper itself

Abstract

Multicellular organisms achieve greater complexity through cell divisions that generate different cell types. We engineered a simple genetic circuit that induces asymmetric cell division and subsequent cell differentiation in Escherichia coli. The circuit involves a scaffolding protein, PopZ, that is stably maintained at a single cell pole over multiple asymmetric cell divisions. PopZ was functionalized to degrade the signaling molecule, c-di-GMP. By regulating synthesis of functionalized PopZ via small molecules or light, we can chemically or optogenetically control the relative abundance of two distinct cell types, characterized by either low or high c-di-GMP levels. Differences in c-di-GMP levels can be transformed into genetically programmable differences in protein complex assembly or gene expression, which in turn produce differential behavior or biosynthetic activities. This study shows emergence of complex biological phenomena from a simple genetic circuit and adds programmable bacterial cell differentiation to the genetic toolbox of synthetic biology and biotechnology.

Indexed as

Asymmetric Cell DivisionBacterial ProteinsCell MovementCloning, MolecularDNA, BacterialEscherichia coliGene Expression Regulation, BacterialSignal TransductionBacterial ProteinsDNA, Bacterial

Identifiers

PMID31406376
PMCPMC7439754
OpenAlexW2968855766

What OpenQuestion holds

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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.