Evidence map›Paper›PMID 41609945›Full record

ArticlePlant biotechnology journal2026

Haploid Mutation Mapping Identifies a Homoeologous Non-Reciprocal Translocation Linked to Reduced Fibre and Enhanced Protein in Brassica napus.

Morgan W Kirzinger, Sarika Saini, Andrea T Todd, Ushan Alahakoon, Kevin C Koh, Justin B Nichol, HaiYing Yuan, Kevin Fengler, Victor Llaca, Dustin Cram and 21 more

Abstract read
In one paragraph

Article in Plant biotechnology journal, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

31 authors.

Morgan W KirzingerAquatic and Crop Resource Development, National Research Council Canada, Saskatoon, Saskatchewan, Canada.
Sarika SainiCorteva Agriscience, Caledon, Ontario, Canada.
Andrea T ToddAquatic and Crop Resource Development, National Research Council Canada, Saskatoon, Saskatchewan, Canada.
Ushan AlahakoonCorteva Agriscience, Saskatoon, Saskatchewan, Canada.
Kevin C KohGlobal Institute for Food Security, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Justin B NicholDepartment of Biological Sciences, University of Calgary, Calgary, Alberta, Canada.
HaiYing YuanAquatic and Crop Resource Development, National Research Council Canada, Saskatoon, Saskatchewan, Canada.ORCID https://orcid.org/0000-0002-4049-3036
Kevin FenglerCorteva Agriscience, Johnston, Iowa, USA.
Victor LlacaCorteva Agriscience, Johnston, Iowa, USA.
Dustin CramAquatic and Crop Resource Development, National Research Council Canada, Saskatoon, Saskatchewan, Canada.
Sampath PerumalGlobal Institute for Food Security, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Wali SoomroAquatic and Crop Resource Development, National Research Council Canada, Saskatoon, Saskatchewan, Canada.
Magda KonopkaAquatic and Crop Resource Development, National Research Council Canada, Saskatoon, Saskatchewan, Canada.
Tancey MelchkartAquatic and Crop Resource Development, National Research Council Canada, Saskatoon, Saskatchewan, Canada.
Venkat BandiDepartment of Computer Science, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Yasmina BekkaouiAquatic and Crop Resource Development, National Research Council Canada, Saskatoon, Saskatchewan, Canada.
Yifang TanAquatic and Crop Resource Development, National Research Council Canada, Saskatoon, Saskatchewan, Canada.
Chad MatsallaAquatic and Crop Resource Development, National Research Council Canada, Saskatoon, Saskatchewan, Canada.
Andrew G SharpeGlobal Institute for Food Security, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Carl GutwinDepartment of Computer Science, University of Saskatchewan, Saskatoon, Saskatchewan, Canada.
Fred ThoonenCorteva Agriscience, Caledon, Ontario, Canada.
Igor FalakCorteva Agriscience, Caledon, Ontario, Canada.
Chad KoscielnyCorteva Agriscience, Carmen, Manitoba, Canada.
Stuart GardnerCorteva Agriscience, Johnston, Iowa, USA.ORCID https://orcid.org/0009-0006-1165-7149
Isobel A P ParkinAgriculture and Agri-Food Canada, Saskatoon, Saskatchewan, Canada.
Marcus A SamuelDepartment of Biological Sciences, University of Calgary, Calgary, Alberta, Canada.ORCID https://orcid.org/0000-0002-3936-5563
Alison M R FerrieAquatic and Crop Resource Development, National Research Council Canada, Saskatoon, Saskatchewan, Canada.
Dave CharneCorteva Agriscience, Caledon, Ontario, Canada.
Daoquan XiangAquatic and Crop Resource Development, National Research Council Canada, Saskatoon, Saskatchewan, Canada.
Jetty S S AmmiRajuCorteva Agriscience, Johnston, Iowa, USA.
Sateesh KagaleAquatic and Crop Resource Development, National Research Council Canada, Saskatoon, Saskatchewan, Canada.ORCID https://orcid.org/0000-0002-7213-1590

Funding

Agriculture Development Fund from the Government of SaskatchewanNational Research Council CanadaPioneer Hi-Bred Production Company
6 · The paper itself

Abstract

A key challenge for the genetic improvement of canola (Brassica napus), one of the world's most important oilseeds, is the limited natural variation for commercially important traits. The creation of new variation is hindered by the lack of functional knowledge about genes controlling these traits. Ploidy and genomic duplications in canola complicate the effective transfer of functional insights from Arabidopsis. Here, we report a novel functional genomics platform for rapid gene/trait discovery and optimisation. We established a double haploid population of 1240 lines from EMS-mutagenised microspores of the spring-type canola line, NRCDH4079. A platinum-quality reference genome, gene annotations and a gene expression atlas from developing seeds were generated for NRCDH4079. Exome sequencing of the mutagenised population resulted in the development of a 'TILLED' database, revealing 1243 premature stop codons across 1222 genes, along with 140 522 moderate-effect or modifier variants impacting 70 626 genes. Phenotypic analysis revealed significant variation in key seed traits, including oil, protein and acid detergent fibre (ADF). Notably, the mutant variant DP125410314 exhibited increased protein and reduced ADF, two important traits for improving the meal composition of canola. Genetic mapping of this variant identified a homoeologous non-reciprocal translocation between A1 and C1 chromosomes associated with reduced ADF content, highlighting the role of structural variations in trait development. This work establishes haploid mutagenesis as a powerful tool for crop improvement, with broader implications for other Brassica species. By enhancing our understanding of seed protein traits, it lays the foundation for canola varieties that meet future nutritional and market demands.

Indexed as

Brassica napusPlant ProteinsTranslocation, GeneticChromosome MappingHaploidyMutationPhenotypeSeedsPlant Proteinsacid detergent fibreBrassica napuscanolaEMShaploid mutagenesisoilproteinstructural variation

Identifiers

PMID41609945
PMCPMC13110153

What OpenQuestion holds

Textmetadata
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.