Evidence map›Paper›PMID 42856025›Full record

ArticleThe Plant journal : for cell and molecular biology2026

The degree and direction of subgenome expression bias in Brassica napus vary between cultivars, tissues and developmental stages.

Hugh Woolfenden, Rachel Wells, Richard J Morris

Abstract read
In one paragraph

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

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

3 authors.

Hugh WoolfendenComputational and Systems Biology, John Innes Centre, Norwich Research Park, Norwich, NR4 7UH, UK.ORCID https://orcid.org/0000-0002-9800-7862
Rachel WellsCrop Genetics, John Innes Centre, Norwich Research Park, Norwich, NR4 7UH, UK.ORCID https://orcid.org/0000-0002-1280-7472
Richard J MorrisComputational and Systems Biology, John Innes Centre, Norwich Research Park, Norwich, NR4 7UH, UK.ORCID https://orcid.org/0000-0003-3080-2613

Funding

BBSRC's Institute Strategic Programme Biotic Interactions underpinning Crop Productivity BB/J004553/1BBSRC's Institute Strategic Programme Building Robustness in Crops BB/X01102X/1BBSRC's Institute Strategic Programme Genes in the Environment BB/P013511/1BBSRC's Institute Strategic Programme Plant Health BB/P012574/1BBSRC Strategic Longer and Larger Grant 'BRAVO' BB/P003095/1
6 · The paper itself

Abstract

Most extant plant lineages show evidence of past polyploidisation events in their genomes. Allopolyploids arise from hybridisation, resulting in polyploid genomes comprising subgenomes from different ancestors. Adaptation to their environment, pre- and post-hybridisation and selection for specific traits has led to several allopolyploids exhibiting an unequal contribution from their subgenomes to phenotypic traits. Associated regulatory changes may have given rise to cultivar-specific subgenome dominance that contributes to the diversity of phenotypes. Likewise, different tissues and developmental stages have distinct expression profiles that may exhibit higher contributions from one subgenome relative to the other. Here, we investigate different metrics for quantifying the contribution of each subgenome to expression in cultivars of Brassica napus, in space (tissue) and time (development). Brassica napus inherited two subgenomes, A and C, from its ancestors Brassica rapa (A) and Brassica oleracea (C). We find that the C subgenome has a larger contribution to transcript abundance than the A subgenome, whereas the mean abundance per expressed gene is higher for the A subgenome. Direct comparison of homoeologous pairs reveals higher expression of genes on the C subgenome. We find that the degree and direction of expression bias can change substantially within a homoeologous pair between cultivars, tissues and across development, suggesting that subgenome dominance is highly dynamic. The quantification of expression bias reveals a strong dependence on the metric and on classification thresholds. These findings help explain contradictory reports on expression bias and subgenome dominance.

Indexed as

Brassica napusGene Expression Regulation, PlantGenome, PlantPolyploidyBrassica napushomoeologue expression biasoilseed rapepolyploidsubgenome dominancetime‐seriestranscriptomics

Identifiers

PMID42856025
PMCPMC13653225

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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.