Evidence map›Paper›PMID 39627497›Full record

ArticleCommunications biology2024

Repeat-induced point mutations driving Parastagonospora nodorum genomic diversity are balanced by selection against non-synonymous mutations.

Darcy A B Jones, Kasia Rybak, Mohitul Hossain, Stefania Bertazzoni, Angela Williams, Kar-Chun Tan, Huyen T T Phan, James K Hane

Abstract read
In one paragraph

Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
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

8 authors.

Darcy A B JonesCentre for Crop & Disease Management, School of Molecular & Life Sciences, Curtin University, Perth, WA, Australia.
Kasia RybakCentre for Crop & Disease Management, School of Molecular & Life Sciences, Curtin University, Perth, WA, Australia.
Mohitul HossainCentre for Crop & Disease Management, School of Molecular & Life Sciences, Curtin University, Perth, WA, Australia.
Stefania BertazzoniCentre for Crop & Disease Management, School of Molecular & Life Sciences, Curtin University, Perth, WA, Australia.
Angela WilliamsCentre for Crop & Disease Management, School of Molecular & Life Sciences, Curtin University, Perth, WA, Australia.
Kar-Chun TanCentre for Crop & Disease Management, School of Molecular & Life Sciences, Curtin University, Perth, WA, Australia.ORCID 0000-0001-6094-823X
Huyen T T PhanCentre for Crop & Disease Management, School of Molecular & Life Sciences, Curtin University, Perth, WA, Australia.ORCID 0000-0002-8971-2308
James K HaneCentre for Crop & Disease Management, School of Molecular & Life Sciences, Curtin University, Perth, WA, Australia. james.hane@curtin.edu.au.ORCID 0000-0002-7651-0977

Funding

Grains Research and Development Corporation (Grains Research & Development Corporation) CUR00023
6 · The paper itself

Abstract

Parastagonospora nodorum is necrotrophic fungal pathogen of wheat with significant genomic resources. Population-level pangenome data for 173 isolates, of which 156 were from Western Australia (WA) and 17 were international, were examined for overall genomic diversity and effector gene content. A heterothallic core population occurred across all regions of WA, with asexually-reproducing clonal clusters in dryer northern regions. High potential for SNP diversity in the form of repeat-induced point mutation (RIP)-like transitions, was observed across the genome, suggesting widespread 'RIP-leakage' from transposon-rich repetitive sequences into non-repetitive regions. The strong potential for RIP-like mutations was balanced by negative selection against non-synonymous SNPs, that was observed within protein-coding regions. Protein isoform profiles of known effector loci (SnToxA, SnTox1, SnTox3, SnTox267, and SnTox5) indicated low-levels of non-synonymous and high-levels of silent RIP-like mutations. Effector predictions identified 186 candidate secreted predicted effector proteins (CSEPs), 69 of which had functional annotations and included confirmed effectors. Pangenome-based effector isoform profiles across WA were distinct from global isolates and were conserved relative to population structure, and may enable new approaches for monitoring crop disease pathotypes.

Indexed as

AscomycotaGenome, FungalPoint MutationFungal ProteinsGenetic VariationPlant DiseasesPolymorphism, Single NucleotideRepetitive Sequences, Nucleic AcidSelection, GeneticTriticumFungal Proteins

Identifiers

PMID39627497
PMCPMC11615325

What OpenQuestion holds

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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.