Evidence map›Paper›PMID 32191325›Full record

ArticleMolecular biology and evolution2020

Unmatched Level of Molecular Convergence among Deeply Divergent Complex Multicellular Fungi.

Zsolt Merényi, Arun N Prasanna, Zheng Wang, Károly Kovács, Botond Hegedüs, Balázs Bálint, Balázs Papp, Jeffrey P Townsend, László G Nagy

Open access · bronzeAbstract read
In one paragraph

Article in Molecular biology and evolution, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
5.3field-weighted citation impact, top 5% 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

19 citing papers in PubMed, 32 citations in OpenAlex.

  1. Adaptive molecular convergence is pervasive across deep time and largely decoupled from phenotypic convergence.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  2. The genetic foundations of convergent traits.Nature reviews. Genetics · 2026
    Review
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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

9 authors at 2 institutions in 2 countries.

Zsolt MerényiSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Center, Szeged, Hungary.
Arun N PrasannaSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Center, Szeged, Hungary.
Zheng WangDepartment of Biostatistics, Yale University, New Haven, CT.
Károly KovácsSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Center, Szeged, Hungary.
Botond HegedüsSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Center, Szeged, Hungary.
Balázs BálintSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Center, Szeged, Hungary.
Balázs PappSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Center, Szeged, Hungary.
Jeffrey P TownsendDepartment of Biostatistics, Yale University, New Haven, CT.
László G NagySynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Center, Szeged, Hungary.
HUN-REN Szegedi Biológiai Kutatóközpont · HUYale University · US

Funding

European Research Council 758161
6 · The paper itself

Abstract

Convergent evolution is pervasive in nature, but it is poorly understood how various constraints and natural selection limit the diversity of evolvable phenotypes. Here, we analyze the transcriptome across fruiting body development to understand the independent evolution of complex multicellularity in the two largest clades of fungi-the Agarico- and Pezizomycotina. Despite >650 My of divergence between these clades, we find that very similar sets of genes have convergently been co-opted for complex multicellularity, followed by expansions of their gene families by duplications. Over 82% of shared multicellularity-related gene families were expanding in both clades, indicating a high prevalence of convergence also at the gene family level. This convergence is coupled with a rich inferred repertoire of multicellularity-related genes in the most recent common ancestor of the Agarico- and Pezizomycotina, consistent with the hypothesis that the coding capacity of ancestral fungal genomes might have promoted the repeated evolution of complex multicellularity. We interpret this repertoire as an indication of evolutionary predisposition of fungal ancestors for evolving complex multicellular fruiting bodies. Our work suggests that evolutionary convergence may happen not only when organisms are closely related or are under similar selection pressures, but also when ancestral genomic repertoires render certain evolutionary trajectories more likely than others, even across large phylogenetic distances.

Indexed as

Biological EvolutionAscomycotaBasidiomycotaFruiting Bodies, FungalGene Expression Regulation, DevelopmentalMultigene Familycomplex multicellularityconvergent evolutionfruiting body developmentfungitranscriptome

Identifiers

PMID32191325
PMCPMC7403615
OpenAlexW3012421156

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.