Evidence map›Paper›PMID 33211093›Full record

ArticleMolecular biology and evolution2021

Genomic Analysis Enlightens Agaricales Lifestyle Evolution and Increasing Peroxidase Diversity.

Francisco J Ruiz-Dueñas, José M Barrasa, Marisol Sánchez-García, Susana Camarero, Shingo Miyauchi, Ana Serrano, Dolores Linde, Rashid Babiker, Elodie Drula, Iván Ayuso-Fernández and 26 more

Open access · hybridAbstract readComparative Study
In one paragraph

Article in Molecular biology and evolution, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 62 papers.

0numbers the graph read from it
0cells of the map it votes in
62citing papers in PubMed
15.8field-weighted citation impact, top 1% 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

62 citing papers in PubMed, 136 citations in OpenAlex.

  1. Review
  2. Hybrid Genome Assembly and Annotation of the Basidiomycete FungusInternational journal of molecular sciences · 2026
    Article
  3. Systematic study ofIMA fungus · 2026
    Article
  4. Article
  5. Article
  6. Chromosome-Level Genome Announcement of the MonokaryoticJournal of fungi (Basel, Switzerland) · 2025
    Article
  7. Review
  8. Review
  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Comparative analyses ofComputational and structural biotechnology journal · 2024
    Article
  17. Article
  18. Article
  19. Article
  20. Article

2 more citing papers are in PubMed but not listed here.

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

36 authors at 12 institutions in 5 countries.

Francisco J Ruiz-DueñasCentro de Investigaciones Biológicas Margarita Salas (CIB), CSIC, Madrid, Spain.
José M BarrasaLife Sciences Department, Alcalá University, Alcalá de Henares, Spain.
Marisol Sánchez-GarcíaBiology Department, Clark University, Worcester, MA, USA.
Susana CamareroCentro de Investigaciones Biológicas Margarita Salas (CIB), CSIC, Madrid, Spain.
Shingo MiyauchiINRAE, Laboratory of Excellence ARBRE, Champenoux, France.
Ana SerranoCentro de Investigaciones Biológicas Margarita Salas (CIB), CSIC, Madrid, Spain.
Dolores LindeCentro de Investigaciones Biológicas Margarita Salas (CIB), CSIC, Madrid, Spain.
Rashid BabikerCentro de Investigaciones Biológicas Margarita Salas (CIB), CSIC, Madrid, Spain.
Elodie DrulaArchitecture et Fonction des Macromolécules Biologiques, CNRS/Aix-Marseille University, Marseille, France.
Iván Ayuso-FernándezCentro de Investigaciones Biológicas Margarita Salas (CIB), CSIC, Madrid, Spain.
Remedios PachecoCentro de Investigaciones Biológicas Margarita Salas (CIB), CSIC, Madrid, Spain.
Guillermo PadillaCentro de Investigaciones Biológicas Margarita Salas (CIB), CSIC, Madrid, Spain.
Patricia FerreiraBiochemistry and Molecular and Cellular Biology Department and BIFI, Zaragoza University, Zaragoza, Spain.
Jorge BarriusoCentro de Investigaciones Biológicas Margarita Salas (CIB), CSIC, Madrid, Spain.
Harald KellnerInternational Institute Zittau, Technische Universität Dresden, Zittau, Germany.
Raúl CastaneraInstitute for Multidisciplinary Research in Applied Biology, IMAB-UPNA, Pamplona, Spain.
Manuel AlfaroInstitute for Multidisciplinary Research in Applied Biology, IMAB-UPNA, Pamplona, Spain.
Lucía RamírezInstitute for Multidisciplinary Research in Applied Biology, IMAB-UPNA, Pamplona, Spain.
Antonio G PisabarroInstitute for Multidisciplinary Research in Applied Biology, IMAB-UPNA, Pamplona, Spain.
Robert RileyUS Department of Energy (DOE) Joint Genome Institute (JGI), Lawrence Berkeley National Lab, Berkeley, CA, USA.
Alan KuoUS Department of Energy (DOE) Joint Genome Institute (JGI), Lawrence Berkeley National Lab, Berkeley, CA, USA.
William AndreopoulosUS Department of Energy (DOE) Joint Genome Institute (JGI), Lawrence Berkeley National Lab, Berkeley, CA, USA.
Kurt LaButtiUS Department of Energy (DOE) Joint Genome Institute (JGI), Lawrence Berkeley National Lab, Berkeley, CA, USA.
Jasmyn PangilinanUS Department of Energy (DOE) Joint Genome Institute (JGI), Lawrence Berkeley National Lab, Berkeley, CA, USA.
Andrew TrittUS Department of Energy (DOE) Joint Genome Institute (JGI), Lawrence Berkeley National Lab, Berkeley, CA, USA.
Anna LipzenUS Department of Energy (DOE) Joint Genome Institute (JGI), Lawrence Berkeley National Lab, Berkeley, CA, USA.
Guifen HeUS Department of Energy (DOE) Joint Genome Institute (JGI), Lawrence Berkeley National Lab, Berkeley, CA, USA.
Mi YanUS Department of Energy (DOE) Joint Genome Institute (JGI), Lawrence Berkeley National Lab, Berkeley, CA, USA.
Vivian NgUS Department of Energy (DOE) Joint Genome Institute (JGI), Lawrence Berkeley National Lab, Berkeley, CA, USA.
Igor V GrigorievUS Department of Energy (DOE) Joint Genome Institute (JGI), Lawrence Berkeley National Lab, Berkeley, CA, USA.
Daniel CullenForest Products Laboratory, US Department of Agriculture, Madison, WI, USA.
Francis MartinINRAE, Laboratory of Excellence ARBRE, Champenoux, France.
Marie-Noëlle RossoINRAE, Biodiversité et Biotechnologie Fongiques, Aix-Marseille University, Marseille, France.
Bernard HenrissatArchitecture et Fonction des Macromolécules Biologiques, CNRS/Aix-Marseille University, Marseille, France.
David HibbettBiology Department, Clark University, Worcester, MA, USA.
Angel T MartínezCentro de Investigaciones Biológicas Margarita Salas (CIB), CSIC, Madrid, Spain.
Centro de Investigaciones Biológicas Margarita Salas · ESJoint Genome Institute · USClark University · USInstitut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement · FRAix-Marseille Université · FRArchitecture et Fonction des Macromolécules Biologiques · FRForest Products Laboratory · USInternational University Institute · DELaboratoire de Recherches sur le Développement de l'Elevage · FRUniversidad de Alcalá · ESUniversidad de Zaragoza · ESUniversity of California, Berkeley · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As actors of global carbon cycle, Agaricomycetes (Basidiomycota) have developed complex enzymatic machineries that allow them to decompose all plant polymers, including lignin. Among them, saprotrophic Agaricales are characterized by an unparalleled diversity of habitats and lifestyles. Comparative analysis of 52 Agaricomycetes genomes (14 of them sequenced de novo) reveals that Agaricales possess a large diversity of hydrolytic and oxidative enzymes for lignocellulose decay. Based on the gene families with the predicted highest evolutionary rates-namely cellulose-binding CBM1, glycoside hydrolase GH43, lytic polysaccharide monooxygenase AA9, class-II peroxidases, glucose-methanol-choline oxidase/dehydrogenases, laccases, and unspecific peroxygenases-we reconstructed the lifestyles of the ancestors that led to the extant lignocellulose-decomposing Agaricomycetes. The changes in the enzymatic toolkit of ancestral Agaricales are correlated with the evolution of their ability to grow not only on wood but also on leaf litter and decayed wood, with grass-litter decomposers as the most recent eco-physiological group. In this context, the above families were analyzed in detail in connection with lifestyle diversity. Peroxidases appear as a central component of the enzymatic toolkit of saprotrophic Agaricomycetes, consistent with their essential role in lignin degradation and high evolutionary rates. This includes not only expansions/losses in peroxidase genes common to other basidiomycetes but also the widespread presence in Agaricales (and Russulales) of new peroxidases types not found in wood-rotting Polyporales, and other Agaricomycetes orders. Therefore, we analyzed the peroxidase evolution in Agaricomycetes by ancestral-sequence reconstruction revealing several major evolutionary pathways and mapped the appearance of the different enzyme types in a time-calibrated species tree.

Indexed as

Genome, FungalPhylogenyAgaricalesEcosystemLigninMultigene FamilyPeroxidasesLigninlignocellulosePeroxidasesAgaricalesancestral-sequence reconstructionlifestyle evolutionligninolytic peroxidaseslignocellulose decayplant cell-wall degrading enzymes

Identifiers

PMID33211093
PMCPMC8480192
OpenAlexW3098236050

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.