Evidence map›Paper›PMID 37595132›Full record

ArticleMolecular biology and evolution2023

Horizontally Transferred DNA in the Genome of the Fungus Pyricularia oryzae is Associated With Repressive Histone Modifications.

Natsuki Kobayashi, Thach An Dang, Kieu Thi Minh Pham, Luis B Gómez Luciano, Ba Van Vu, Kosuke Izumitsu, Motoki Shimizu, Ken-Ichi Ikeda, Wen-Hsiung Li, Hitoshi Nakayashiki

Open access · goldAbstract read
In one paragraph

Article in Molecular biology and evolution, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.5field-weighted citation impact, top 7% 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

7 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Horizontal Gene Transfer in Plants and Implications for Biotechnology.Plant-environment interactions (Hoboken, N.J.) · 2025
    Review
  3. Article
  4. Article
  5. Current research in microbial sciences · 2025
    Article
  6. Article
  7. 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

10 authors at 6 institutions in 3 countries.

Natsuki KobayashiGraduate School of Agricultural Science, Kobe University, Kobe, Japan.
Thach An DangGraduate School of Agricultural Science, Kobe University, Kobe, Japan.
Kieu Thi Minh PhamGraduate School of Agricultural Science, Kobe University, Kobe, Japan.
Luis B Gómez LucianoBiodiversity Research Center, Academia Sinica, Taipei, Taiwan.
Ba Van VuGraduate School of Agricultural Science, Kobe University, Kobe, Japan.
Kosuke IzumitsuGraduate School of Environmental Science, The University of Shiga Prefecture, Hikone, Japan.
Motoki ShimizuDepartment of Genomics and Breeding, Iwate Biotechnology Research Center, Kitakami, Japan.ORCID 0000-0002-5622-5554
Ken-Ichi IkedaGraduate School of Agricultural Science, Kobe University, Kobe, Japan.
Wen-Hsiung LiBiodiversity Research Center, Academia Sinica, Taipei, Taiwan.
Hitoshi NakayashikiGraduate School of Agricultural Science, Kobe University, Kobe, Japan.
Kobe University · JPBaylor College of Medicine · USDonald Danforth Plant Science Center · USIwate Biotechnology Research Center · JPUniversity of Chicago · USUniversity of Shiga Prefecture · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Horizontal gene transfer (HGT) is a means of exchanging genetic material asexually. The process by which horizontally transferred genes are domesticated by the host genome is of great interest but is not well understood. In this study, we determined the telomere-to-telomere genome sequence of the wheat-infecting Pyricularia oryzae strain Br48. SNP analysis indicated that the Br48 strain is a hybrid of wheat- and Brachiaria-infecting strains by a sexual or parasexual cross. Comparative genomic analysis identified several megabase-scale "insertions" in the Br48 genome, some of which were possibly gained by HGT-related events from related species, such as P. pennisetigena or P. grisea. Notably, the mega-insertions often contained genes whose phylogeny is not congruent with the species phylogeny. Moreover, some of the genes have a close homolog even in distantly related organisms, such as basidiomycetes or prokaryotes, implying the involvement of multiple HGT events. Interestingly, the levels of the silent epigenetic marks H3K9me3 and H3K27me3 in a genomic region tended to be negatively correlated with the phylogenetic concordance of genes in the same region, suggesting that horizontally transferred DNA is preferentially targeted for epigenetic silencing. Indeed, the putative HGT-derived genes were activated when MoKmt6, the gene responsible for H3K27me3 modification, was deleted. Notably, these genes also tended to be up-regulated during infection, suggesting that they are now under host control and have contributed to establishing a fungal niche. In conclusion, this study suggests that epigenetic modifications have played an important role in the domestication of HGT-derived genes in the P. oryzae genome.

Indexed as

AscomycotaHistone CodeDNAHistonesPhylogenyTriticumDNAHistonesepigeneticshorizontal gene transferphytopathogenic fungi

Identifiers

PMID37595132
PMCPMC10473863
OpenAlexW4385971545

What OpenQuestion holds

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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.