Evidence map›Paper›PMID 37498334›Full record

ArticleGenome biology and evolution2023

Insights into the Ecological Diversification of the Hymenochaetales based on Comparative Genomics and Phylogenomics With an Emphasis on Coltricia.

Heng Zhao, Yu-Cheng Dai, Fang Wu, Xiao-Yong Liu, Sundy Maurice, Konstantin V Krutovsky, Igor N Pavlov, Daniel L Lindner, Francis M Martin, Yuan Yuan

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
8.3field-weighted citation impact, top 3% 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

13 citing papers in PubMed, 21 citations in OpenAlex.

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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

10 authors at 7 institutions in 6 countries.

Heng ZhaoInstitute of Microbiology, School of Ecology and Nature Conservation, Beijing Forestry University, Beijing, China.ORCID 0000-0003-2938-5613
Yu-Cheng DaiInstitute of Microbiology, School of Ecology and Nature Conservation, Beijing Forestry University, Beijing, China.
Fang WuInstitute of Microbiology, School of Ecology and Nature Conservation, Beijing Forestry University, Beijing, China.
Xiao-Yong LiuCollege of Life Sciences, Shandong Normal University, Jinan, China.
Sundy MauriceSection for Genetics and Evolutionary Biology (EVOGENE), Department of Biosciences, University of Oslo, Oslo, Norway.
Konstantin V KrutovskyDepartment of Forest Genetics and Forest Tree Breeding, Georg-August University of Göttingen, Göttingen, Germany.
Igor N PavlovMycology and Plant Pathology, V.N. Sukachev Institute of Forest SB RAS, Krasnoyarsk, Russia.
Daniel L LindnerCenter for Forest Mycology Research, Madison, Wisconsin, USA.
Francis M MartinUniversité de Lorraine, INRAE, UMR Interactions Arbres/Microorganismes, Centre INRAE-GrandEst-Nancy, Champenoux, France.
Yuan YuanInstitute of Microbiology, School of Ecology and Nature Conservation, Beijing Forestry University, Beijing, China.ORCID 0000-0001-6674-9848
Beijing Forestry University · CNForest Products Laboratory · USInstitut National de Recherche pour l'Agriculture, l'Alimentation et l'Environnement · FRShandong Normal University · CNSukachev Institute of Forest · RUUniversity of Oslo · NOVoronezh State University of Forestry and Technologies · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

To elucidate the genomic traits of ecological diversification in the Hymenochaetales, we sequenced 15 new genomes, with attention to ectomycorrhizal (EcM) Coltricia species. Together with published data, 32 genomes, including 31 Hymenochaetales and one outgroup, were comparatively analyzed in total. Compared with those of parasitic and saprophytic members, EcM species have significantly reduced number of plant cell wall degrading enzyme genes, and expanded transposable elements, genome sizes, small secreted proteins, and secreted proteases. EcM species still retain some of secreted carbohydrate-active enzymes (CAZymes) and have lost the key secreted CAZymes to degrade lignin and cellulose, while possess a strong capacity to degrade a microbial cell wall containing chitin and peptidoglycan. There were no significant differences in secreted CAZymes between fungi growing on gymnosperms and angiosperms, suggesting that the secreted CAZymes in the Hymenochaetales evolved before differentiation of host trees into gymnosperms and angiosperms. Nevertheless, parasitic and saprophytic species of the Hymenochaetales are very similar in many genome features, which reflect their close phylogenetic relationships both being white rot fungi. Phylogenomic and molecular clock analyses showed that the EcM genus Coltricia formed a clade located at the base of the Hymenochaetaceae and divergence time later than saprophytic species. And Coltricia remains one to two genes of AA2 family. These indicate that the ancestors of Coltricia appear to have originated from saprophytic ancestor with the ability to cause a white rot. This study provides new genomic data for EcM species and insights into the ecological diversification within the Hymenochaetales based on comparative genomics and phylogenomics analyses.

Indexed as

BasidiomycotaMycorrhizaeGenomicsLigninPhylogenyLigninColtriciaecological diversitygenomicsHymenochaetaceaetransposable elementswhite rot

Identifiers

PMID37498334
PMCPMC10410303
OpenAlexW4385295296

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.