Evidence map›Paper›PMID 32058961›Full record

ArticleiScience2020

Inferring Biochemical Reactions and Metabolite Structures to Understand Metabolic Pathway Drift.

Arnaud Belcour, Jean Girard, Méziane Aite, Ludovic Delage, Camille Trottier, Charlotte Marteau, Cédric Leroux, Simon M Dittami, Pierre Sauleau, Erwan Corre and 6 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. The genus Serratia revisited by genomics.Nature communications · 2022
    Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. 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

16 authors at 2 institutions in 1 country.

Arnaud BelcourUniv Rennes, Inria, CNRS, IRISA, Equipe Dyliss, Rennes, France.
Jean GirardSorbonne Université, CNRS, Integrative Biology of Marine Models (LBI2M, UMR8227), Station Biologique de Roscoff (SBR), 29680 Roscoff, France.
Méziane AiteUniv Rennes, Inria, CNRS, IRISA, Equipe Dyliss, Rennes, France.
Ludovic DelageSorbonne Université, CNRS, Integrative Biology of Marine Models (LBI2M, UMR8227), Station Biologique de Roscoff (SBR), 29680 Roscoff, France.
Camille TrottierUniv Rennes, Inria, CNRS, IRISA, Equipe Dyliss, Rennes, France.
Charlotte MarteauLBCM, IUEM, University of Bretagne-Sud, Lorient, France.
Cédric LerouxSorbonne Université, CNRS, Plateforme METABOMER-Corsaire (FR2424), Station Biologique de Roscoff, Roscoff, France.
Simon M DittamiSorbonne Université, CNRS, Integrative Biology of Marine Models (LBI2M, UMR8227), Station Biologique de Roscoff (SBR), 29680 Roscoff, France.
Pierre SauleauLBCM, IUEM, University of Bretagne-Sud, Lorient, France.
Erwan CorreSorbonne Université, CNRS, Plateforme ABiMS (FR2424), Station Biologique de Roscoff, Roscoff, France.
Jacques NicolasUniv Rennes, Inria, CNRS, IRISA, Equipe Dyliss, Rennes, France.
Catherine BoyenSorbonne Université, CNRS, Integrative Biology of Marine Models (LBI2M, UMR8227), Station Biologique de Roscoff (SBR), 29680 Roscoff, France.
Catherine LeblancSorbonne Université, CNRS, Integrative Biology of Marine Models (LBI2M, UMR8227), Station Biologique de Roscoff (SBR), 29680 Roscoff, France.
Jonas CollénSorbonne Université, CNRS, Integrative Biology of Marine Models (LBI2M, UMR8227), Station Biologique de Roscoff (SBR), 29680 Roscoff, France.
Anne SiegelUniv Rennes, Inria, CNRS, IRISA, Equipe Dyliss, Rennes, France.
Gabriel V MarkovSorbonne Université, CNRS, Integrative Biology of Marine Models (LBI2M, UMR8227), Station Biologique de Roscoff (SBR), 29680 Roscoff, France. Electronic address: gabriel.markov@sb-roscoff.fr.
Centre National de la Recherche Scientifique · FRUniversité de Bretagne Sud · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inferring genome-scale metabolic networks in emerging model organisms is challenged by incomplete biochemical knowledge and partial conservation of biochemical pathways during evolution. Therefore, specific bioinformatic tools are necessary to infer biochemical reactions and metabolic structures that can be checked experimentally. Using an integrative approach combining genomic and metabolomic data in the red algal model Chondrus crispus, we show that, even metabolic pathways considered as conserved, like sterols or mycosporine-like amino acid synthesis pathways, undergo substantial turnover. This phenomenon, here formally defined as "metabolic pathway drift," is consistent with findings from other areas of evolutionary biology, indicating that a given phenotype can be conserved even if the underlying molecular mechanisms are changing. We present a proof of concept with a methodological approach to formalize the logical reasoning necessary to infer reactions and molecular structures, abstracting molecular transformations based on previous biochemical knowledge.

Indexed as

BioinformaticsGenomicsMetabolomics

Identifiers

PMID32058961
PMCPMC6997860
OpenAlexW3000039767

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.