4.6 Article

Uneven Levels of 5S and 45S rDNA Site Number and Loci Variations across Wild Chrysanthemum Accessions

Journal

GENES
Volume 13, Issue 5, Pages -

Publisher

MDPI
DOI: 10.3390/genes13050894

Keywords

Chrysanthemum; Asteraceae; 5S rDNA; 45S rDNA; oligonucleotide fluorescence in situ hybridization (Oligo-FISH)

Funding

  1. National Natural Science Foundation of China [32172613]
  2. Natural Science Foundation of Jiangsu Province [BK20211215]
  3. Fundamental Research Funds for the Central Universities
  4. Priority Academic Program Development of Jiangsu Higher Education Institutions

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This study used oligonucleotide fluorescence in situ hybridization (Oligo-FISH) to draw ideograms of rDNA sites in Chrysanthemum accessions and found polymorphisms and co-localization of rDNA sites. There was also a correlation between the number of 5S rDNA sites and chromosome number, and the geographical distribution of different ploidy Chrysanthemum accessions may have promoted karyotype evolution. The study identified the formation mechanism of rDNA variations and provided a reliable method for examining rDNA variations in Chrysanthemum and related species, contributing to understanding the evolutionary and phylogenetic relationships of the Chrysanthemum genus.
Ribosomal DNA (rDNA) is an excellent cytogenetic marker owing to its tandem arrangement and high copy numbers. However, comparative studies have focused more on the number of rDNA site variations within the Chrysanthemum genus, and studies on the types of rDNA sites with the same experimental procedures at the species levels are lacking. To further explore the number and types of rDNA site variations, we combined related data to draw ideograms of the rDNA sites of Chrysanthemum accessions using oligonucleotide fluorescence in situ hybridization (Oligo-FISH). Latent variations (such as polymorphisms of 45S rDNA sites and co-localized 5S-45S rDNA) also occurred among the investigated accessions. Meanwhile, a significant correlation was observed between the number of 5S rDNA sites and chromosome number. Additionally, the clumped and concentrated geographical distribution of different ploidy Chrysanthemum accessions may significantly promote the karyotype evolution. Based on the results above, we identified the formation mechanism of rDNA variations. Furthermore, these findings may provide a reliable method to examine the sites and number of rDNA variations among Chrysanthemum and its related accessions and allow researchers to further understand the evolutionary and phylogenetic relationships of the Chrysanthemum genus.

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