Evidence map›Paper›PMID 40052422›Full record

ArticleGenome biology and evolution2025

Tracing the Origin and Evolution of the Fungal Mycophenolic Acid Biosynthesis Pathway.

Baptiste Bidon, Hajar Yaakoub, Arnaud Lanoue, Antoine Géry, Virginie Séguin, Florent Magot, Claire Hoffmann, Vincent Courdavault, Jean-Philippe Bouchara, Jean-Pierre Gangneux and 8 more

Abstract read
In one paragraph

Article in Genome biology and evolution, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

18 authors.

Baptiste BidonUniv Angers, Univ Brest, IRF, SFR ICAT, F-49000 Angers, France.ORCID 0000-0003-0113-8717
Hajar YaakoubUniv Angers, Univ Brest, IRF, SFR ICAT, F-49000 Angers, France.ORCID 0000-0001-8467-6021
Arnaud LanoueUniversité de Tours, BBV EA2106, Tours, France.ORCID 0000-0002-7377-8177
Antoine GéryABTE EA 4651-ToxEMAC, Normandie Université, UNICAEN, UNIROUEN, Caen, France.ORCID 0000-0002-3144-9260
Virginie SéguinABTE EA 4651-ToxEMAC, Normandie Université, UNICAEN, UNIROUEN, Caen, France.ORCID 0009-0000-5097-6966
Florent MagotUniversité de Tours, BBV EA2106, Tours, France.ORCID 0009-0009-2433-9950
Claire HoffmannUniv Angers, Univ Brest, IRF, SFR ICAT, F-49000 Brest, France.
Vincent CourdavaultUniversité de Tours, BBV EA2106, Tours, France.ORCID 0000-0001-8902-4532
Jean-Philippe BoucharaUniv Angers, Univ Brest, IRF, SFR ICAT, F-49000 Angers, France.ORCID 0000-0001-8047-9506
Jean-Pierre GangneuxUniv Rennes, CHU Rennes, Inserm, EHESP, Irset (Institut de recherche en santé, environnement et travail)-UMR_S 1085, Rennes, France.ORCID 0000-0002-4974-5607
Jens C FrisvadDepartment of Biotechnology and Biomedicine, Technical University of Denmark, Kongens Lyngby, Denmark.ORCID 0000-0002-0573-4340
Antonis RokasDepartment of Biological Sciences, Vanderbilt University, Nashville, TN, USA.ORCID 0000-0002-7248-6551
Gustavo H GoldmanFaculdade de Ciências Farmacêuticas de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, Brazil.ORCID 0000-0002-2986-350X
Gilles NevezUniv Angers, Univ Brest, IRF, SFR ICAT, F-49000 Brest, France.ORCID 0000-0001-5888-6017
Solène Le GalUniv Angers, Univ Brest, IRF, SFR ICAT, F-49000 Brest, France.ORCID 0000-0003-0747-9571
Domenico DavolosDepartment of Technological Innovations and Safety of Plants, Products and Anthropic Settlements (DIT), INAIL Research Area, Rome, Italy.ORCID 0000-0002-1728-2740
David GaronABTE EA 4651-ToxEMAC, Normandie Université, UNICAEN, UNIROUEN, Caen, France.ORCID 0000-0003-3545-6641
Nicolas PaponUniv Angers, Univ Brest, IRF, SFR ICAT, F-49000 Angers, France.ORCID 0000-0001-6265-7321

Funding

Deciphering the phenotypic and genomic traits that underlie the evolution of pathogenicity differences among Aspergillus fumigatus and its close relativesR01AI153356 · NIAID · VANDERBILT UNIVERSITY · PI Antonis Rokas · 2022 to 2026
$3.5M
Agence Nationale de la Recherche ANR-24-CE15-2995-01Angers Loire MétropoleBurroughs Wellcome FundConseil Régional des Pays de la LoireHORIZON-CL6-2023-CircBio-01-11INAIL-DIT Research AreaNational Science Foundation DEB-2110404NIAID NIH HHS R01 AI153356NIH HHS
6 · The paper itself

Abstract

Like bacteria and plants, fungi produce a remarkable diversity of small molecules with potent activities for human health known as natural products or secondary metabolites. One such example is mycophenolic acid, a powerful immunosuppressant drug that is administered daily to millions of transplant recipients worldwide. Production of mycophenolic acid is restricted to a very limited number of filamentous fungi, and little is known about its biosynthetic modalities. It is therefore a particular challenge to improve our knowledge of the biosynthesis of this valuable natural compound, as this would contribute to a better understanding of the specialized metabolism of fungi and could also lead to the identification of new fungal producers for the supply of immunosuppressants. Here, we were interested in deciphering the origin and evolution of the fungal mycophenolic acid biosynthetic pathway. Large-scale analyses of fungal genomic resources led us to identify several new species that harbor a gene cluster for mycophenolic acid biosynthesis. Phylogenomic analysis suggests that the mycophenolic acid biosynthetic gene cluster originated early in a common ancestor of the fungal family Aspergillaceae but was repeatedly lost and it is now present in a narrow but diverse set of filamentous fungi. Moreover, a comparison of the inosine 5'-monophosphate dehydrogenase protein sequences that are the target of the mycophenolic acid drug as well as analysis of mycophenolic acid production and susceptibility suggest that all mycophenolic acid fungal producers are resistant to this toxic compound, but that this resistance is likely to be based on different molecular mechanisms. Our study provides new insight into the evolution of the biosynthesis of the important secondary metabolite mycophenolic acid in fungi.

Indexed as

Biosynthetic PathwaysEvolution, MolecularFungiMycophenolic AcidGenome, FungalMultigene FamilyPhylogenyMycophenolic Acidantifungalbiosynthesisbiosynthetic pathwayimmunosuppressantsecondary metabolism

Identifiers

PMID40052422
PMCPMC11934065

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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.