Evidence map›Paper›PMID 29672509›Full record

ArticlePLoS genetics2018

Robustness encoded across essential and accessory replicons of the ecologically versatile bacterium Sinorhizobium meliloti.

George C diCenzo, Alex B Benedict, Marco Fondi, Graham C Walker, Turlough M Finan, Alessio Mengoni, Joel S Griffitts

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
11.2field-weighted citation impact, top 2% 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

34 citing papers in PubMed, 63 citations in OpenAlex.

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  16. Diversification of plasmids in a genus of pathogenic and nitrogen-fixing bacteria.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2022
    Article
  17. Article
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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 4 institutions in 3 countries.

George C diCenzoDepartment of Biology, University of Florence, Sesto Fiorentino, FI, Italy.ORCID 0000-0003-3889-6570
Alex B BenedictDepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT, United States of America.ORCID 0000-0002-4801-2989
Marco FondiDepartment of Biology, University of Florence, Sesto Fiorentino, FI, Italy.ORCID 0000-0001-9291-5467
Graham C WalkerDepartment of Biology, Massachusetts Institute of Technology, Cambridge, MA, United States of America.
Turlough M FinanDepartment of Biology, McMaster University, Hamilton, ON, Canada.
Alessio MengoniDepartment of Biology, University of Florence, Sesto Fiorentino, FI, Italy.
Joel S GriffittsDepartment of Microbiology and Molecular Biology, Brigham Young University, Provo, UT, United States of America.
University of Florence · ITBrigham Young University · USMassachusetts Institute of Technology · USMcMaster University · CA

Funding

MOLEULAR GENETICS OF RHIZOBIUM PLASMIDSR01GM031030 · NIGMS · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI WALKER, GRAHAM C · 1985 to 2020
$8.6M
NIGMS NIH HHS R01 GM031030
6 · The paper itself

Abstract

Bacterial genome evolution is characterized by gains, losses, and rearrangements of functional genetic segments. The extent to which large-scale genomic alterations influence genotype-phenotype relationships has not been investigated in a high-throughput manner. In the symbiotic soil bacterium Sinorhizobium meliloti, the genome is composed of a chromosome and two large extrachromosomal replicons (pSymA and pSymB, which together constitute 45% of the genome). Massively parallel transposon insertion sequencing (Tn-seq) was employed to evaluate the contributions of chromosomal genes to growth fitness in both the presence and absence of these extrachromosomal replicons. Ten percent of chromosomal genes from diverse functional categories are shown to genetically interact with pSymA and pSymB. These results demonstrate the pervasive robustness provided by the extrachromosomal replicons, which is further supported by constraint-based metabolic modeling. A comprehensive picture of core S. meliloti metabolism was generated through a Tn-seq-guided in silico metabolic network reconstruction, producing a core network encompassing 726 genes. This integrated approach facilitated functional assignments for previously uncharacterized genes, while also revealing that Tn-seq alone missed over a quarter of wild-type metabolism. This work highlights the many functional dependencies and epistatic relationships that may arise between bacterial replicons and across a genome, while also demonstrating how Tn-seq and metabolic modeling can be used together to yield insights not obtainable by either method alone.

Indexed as

Genome, BacterialRepliconComputer SimulationConserved SequenceDNA, BacterialDNA Transposable ElementsEcosystemEpistasis, GeneticEvolution, MolecularGenetic Association StudiesHigh-Throughput Nucleotide SequencingMetabolic Networks and PathwaysModels, GeneticMolecular Sequence AnnotationMutationSequence Analysis, DNADNA, BacterialDNA Transposable Elements

Identifiers

PMID29672509
PMCPMC5929573
OpenAlexW2802955747

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.