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When fathers are instant losers: homogenization of rDNA loci in recently formed Cardamine × schulzii trigenomic allopolyploid. | LitMetric

AI Article Synopsis

  • Recent allopolyploids, like Cardamine × schulzii, provide insights into how hybridization and genomic duplication affect evolution and genome structure.
  • The study focused on analyzing the 35SrRNA genes using various methods like next-generation sequencing and RT-PCR, revealing maternal bias in gene ratios.
  • Findings suggest that certain rDNA loci are being reestablished in C. × schulzii through translocation, and the use of NGS enhances our understanding of the evolution of allopolyploid species.

Article Abstract

Recently formed allopolyploids represent an excellent system to study the impacts of hybridization and genomic duplication on genome structure and evolution. Here we explored the 35SrRNA genes (rDNA) in the Cardamine × schulzii allohexaploid that was formed by two subsequent hybridization events within the past c. 150 yr. The rDNA loci were analyzed by cloning, next generation sequencing (NGS), RT-PCR and FISH methods. The primary C. × insueta triploid hybrid derived from C. rivularis (♀) and C. amara (♂) had gene ratios highly skewed towards maternal sequences. Similarly, C. × schulzii, originating from the secondary hybridization event involving C. × insueta (♀) and C. pratensis (♂), showed a reduction in paternal rDNA homeologs despite an excess of chromosomes inherited from C. pratensis. We also identified novel rDNA loci in C. × schulzii, suggesting that lost loci might be slowly reinstalled by translocation (but not recombination) of genes from partner genomes. Prevalent clonal propagation of allopolyploids, C. × insueta and C. × schulzii, indicates that concerted evolution of rDNA may occur in the absence of extensive meiotic cycles. Adoption of NGS in rDNA variant analysis is highly informative for deciphering the evolutionary histories of allopolyploid species with ongoing homogenization processes.

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Source
http://dx.doi.org/10.1111/nph.12873DOI Listing

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