# Evolutionary history and genomic consequences of polyploidization in natural populations of Orychophragmus taibaiensis

**Authors:** Qiang Lai, Zeng Wang, Changfu Jia, Xiner Qumu, Rui Wang, Zhipeng Zhao, Yao Liu, Yukang Hou, Jianquan Liu, Pär K Ingvarsson, Jing Wang

PMC · DOI: 10.1093/hr/uhaf314 · Horticulture Research · 2025-11-08

## TL;DR

This study explores how genome doubling in a plant species affects genetic diversity and evolution, revealing that tetraploids accumulate more harmful mutations and show changes in gene expression.

## Contribution

The study provides new insights into the genomic consequences of polyploidization in natural populations of Orychophragmus taibaiensis.

## Key findings

- Tetraploids in Orychophragmus taibaiensis accumulated a higher genetic load of deleterious mutations.
- Genome doubling was associated with pronounced changes in gene expression patterns.
- Relaxed purifying selection and allelic redundancy likely contribute to the evolutionary potential of polyploids.

## Abstract

Polyploidization has occurred throughout the tree of life and is particularly common in plants. Despite its ubiquity, our understanding of the short- and long-term effects and consequences of genome doubling in natural populations remains incomplete. In this study, we identified a novel ploidy-variable species system within the ornamental and industrial oilseed genus Orychophragmus (Brassicaceae), which comprises six species, including diploid and tetraploid cytotypes of Orychophragmus taibaiensis. By integrating population-scale genomic and transcriptomic datasets across the species in this genus, we constructed a robust phylogenetic framework and investigated the divergence and demographic history of O. taibaiensis in comparison to its relatives. Specifically, we characterized the geographical distribution patterns of diploids and tetraploids in natural populations of O. taibaiensis, confirmed the autopolyploid origin of tetraploids, and inferred their origin time relative to diploid counterparts. Our findings further revealed that, following genome doubling, tetraploids accumulated a higher genetic load of deleterious mutations, likely due to relaxed purifying selection facilitated by allelic redundancy. Additionally, genome doubling was associated with pronounced changes in gene expression patterns, with differentially expressed genes evolving under relaxed selective constraints. These results highlight that the initial masking of deleterious mutations, changes in expression regulation, and divergent efficacy of selection likely all contribute to shaping the establishment and evolutionary potential of polyploids.

## Linked entities

- **Species:** Orychophragmus taibaiensis (taxon 1517519)

## Full-text entities

- **Genes:** AT3G12320 (uncharacterized protein) [NCBI Gene 820411] {aka LNK3, night light-inducible and clock-regulated 3}, DME (HhH-GPD base excision DNA repair family protein) [NCBI Gene 830335] {aka AT5G04570, AT5G04580, DEMETER, T32M21.160, T32M21_160}, PAD4 (alpha/beta-Hydrolases superfamily protein) [NCBI Gene 824408] {aka ARABIDOPSIS PHYTOALEXIN DEFICIENT 4, ATPAD4, PHYTOALEXIN DEFICIENT 4}, SNI1 (negative regulator of systemic acquired resistance (SNI1)) [NCBI Gene 827577] {aka F28J12.3, F28J12_3, INDUCIBLE 1, SUPPRESSOR OF NPR1-1}, XTH7 (xyloglucan endotransglucosylase/hydrolase 7) [NCBI Gene 829936] {aka T28I19.80, T28I19_80, xyloglucan endotransglucosylase/hydrolase 7}, RECA2 (recA DNA recombination family protein) [NCBI Gene 816468] {aka A. thaliana recA homolog 2, F3P11.9, F3P11_9}, CERK1 (chitin elicitor receptor kinase 1) [NCBI Gene 821717] {aka AtCERK1, AtLYK1, LYK1, LYSM DOMAIN RECEPTOR-LIKE KINASE 1, LYSM RLK1, LysM-containing receptor-like kinase 1}, EXT3 (extensin 3) [NCBI Gene 838728] {aka ATEXT3, F16F4.4, F16F4_4, ROOT-SHOOT-HYPOCOTYL DEFECTIVE, RSH, extensin 3}
- **Diseases:** MH (MESH:C535694), LGM (MESH:C536089), disease (MESH:D004194)
- **Chemicals:** oil (MESH:D009821), fatty acid (MESH:D005227), fuchsin (MESH:D012394), silica (MESH:D012822), alpha-DOX1 (-), reactive oxygen species (MESH:D017382), jasmonic acid (MESH:C011006), polyamine (MESH:D011073), nitrogen (MESH:D009584), salicylic acid (MESH:D020156), ethanol (MESH:D000431), acetic acid (MESH:D019342), HCl (MESH:D006851), colchicine (MESH:D003078), carbol (MESH:D019800)
- **Species:** Orychophragmus zhongtiaoshanus (species) [taxon 1931380], Brassica rapa (field mustard, species) [taxon 3711], Arabidopsis thaliana (mouse-ear cress, species) [taxon 3702], Orychophragmus diffusus (species) [taxon 1517517], Sinalliaria limprichtiana (species) [taxon 1920187], Orychophragmus hupehensis (species) [taxon 1517518], Arabidopsis lyrata (lyrate rockcress, species) [taxon 59689], Orychophragmus taibaiensis (species) [taxon 1517519], Raphanus sativus (radish, species) [taxon 3726], Capsella rubella (species) [taxon 81985], Orychophragmus (genus) [taxon 71233], Aethionema arabicum (species) [taxon 228871], Sinalliaria (genus) [taxon 1920186]
- **Cell lines:** S2 — Drosophila melanogaster (Fruit fly), Spontaneously immortalized cell line (CVCL_Z232)

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12946681/full.md

## References

117 references — full list in the complete paper: https://tomesphere.com/paper/PMC12946681/full.md

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Source: https://tomesphere.com/paper/PMC12946681