Evidence map›Paper›PMID 37431308›Full record

ArticlePlant biotechnology journal2023

Comparative pangenome analyses provide insights into the evolution of Brassica rapa resistance gene analogues (RGAs).

Junrey C Amas, Philipp E Bayer, Wei Hong Tan, Soodeh Tirnaz, William J W Thomas, David Edwards, Jacqueline Batley

Open access · goldAbstract read
In one paragraph

Article in Plant biotechnology journal, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
5.6field-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

11 citing papers in PubMed, 14 citations in OpenAlex.

  1. Structural Variation and Its Roles in Plant Genomes.Plants (Basel, Switzerland) · 2026
    Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. ExploitingPlants (Basel, Switzerland) · 2024
    Review
  9. Review
  10. Breeding and management of major resistance genes to stem canker/blackleg in Brassica crops.TAG. Theoretical and applied genetics. Theoretische und angewandte Genetik · 2024
    Review
  11. 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

7 authors at 1 institution in 1 country.

Junrey C AmasSchool of Biological Sciences and the Institute of Agriculture, The University of Western Australia, Crawley, WA, Australia.ORCID 0000-0002-2179-5557
Philipp E BayerSchool of Biological Sciences and the Institute of Agriculture, The University of Western Australia, Crawley, WA, Australia.ORCID 0000-0001-8530-3067
Wei Hong TanSchool of Biological Sciences and the Institute of Agriculture, The University of Western Australia, Crawley, WA, Australia.
Soodeh TirnazSchool of Biological Sciences and the Institute of Agriculture, The University of Western Australia, Crawley, WA, Australia.ORCID 0000-0002-6100-1790
William J W ThomasSchool of Biological Sciences and the Institute of Agriculture, The University of Western Australia, Crawley, WA, Australia.ORCID 0000-0002-5147-8704
David EdwardsSchool of Biological Sciences and the Centre for Applied Bioinformatics, The University of Western Australia, Crawley, WA, Australia.ORCID 0000-0001-7599-6760
Jacqueline BatleySchool of Biological Sciences and the Institute of Agriculture, The University of Western Australia, Crawley, WA, Australia.ORCID 0000-0002-5391-5824
The University of Western Australia · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brassica rapa is grown worldwide as economically important vegetable and oilseed crop. However, its production is challenged by yield-limiting pathogens. The sustainable control of these pathogens mainly relies on the deployment of genetic resistance primarily driven by resistance gene analogues (RGAs). While several studies have identified RGAs in B. rapa, these were mainly based on a single genome reference and do not represent the full range of RGA diversity in B. rapa. In this study, we utilized the B. rapa pangenome, constructed from 71 lines encompassing 12 morphotypes, to describe a comprehensive repertoire of RGAs in B. rapa. We show that 309 RGAs were affected by presence-absence variation (PAV) and 223 RGAs were missing from the reference genome. The transmembrane leucine-rich repeat (TM-LRR) RGA class had more core gene types than variable genes, while the opposite was observed for nucleotide-binding site leucine-rich repeats (NLRs). Comparative analysis with the B. napus pangenome revealed significant RGA conservation (93%) between the two species. We identified 138 candidate RGAs located within known B. rapa disease resistance QTL, of which the majority were under negative selection. Using blackleg gene homologues, we demonstrated how these genes in B. napus were derived from B. rapa. This further clarifies the genetic relationship of these loci, which may be useful in narrowing-down candidate blackleg resistance genes. This study provides a novel genomic resource towards the identification of candidate genes for breeding disease resistance in B. rapa and its relatives.

Indexed as

Brassica napusBrassica rapaDisease ResistanceGenes, PlantLeucinePlant BreedingLeucineblackleg resistanceBrassica evolutionBrassica genomicspangenomePresence absence variation (PAV)resistance gene analogue (RGA)structural variation (SV)

Identifiers

PMID37431308
PMCPMC10502758
OpenAlexW4383872517

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.