Chromosomal Localization and Diversity Analysis of 5S and 18S Ribosomal DNA in 13 Species from the Genus Ipomoea

<b>Background:</b> Sweet potato (<i>Ipomoea batatas</i> (L.) Lam.), a key global root crop, faces challenges due to its narrow genetic background. This issue can be addressed by utilizing the diverse genetic resources of sweet potato's wild relatives, which are invaluable for its genetic improvement. <b>Methods:</b> The morphological differences in leaves, stems, and roots among 13 <i>Ipomoea</i> species were observed and compared. Chromosome numbers were determined by examining metaphase cells from root tips. Fluorescence in situ hybridization (FISH) was used to identify the number of 5S and 18S rDNA sites in these species. PCR amplification was performed for both 5S and 18S rDNA, and phylogenetic relationships among the species were analyzed based on the sequences of 18S rDNA. <b>Results:</b> Three species were found to have enlarged roots among the 13 <i>Ipomoea</i> species. Chromosome analysis revealed that <i>I. batatas</i> had 90 chromosomes, <i>Ipomoea pes-tigridis</i> had 28 chromosomes, while the remaining species possessed 30 chromosomes. Detection of rDNA sites in the 13 species showed two distinct 5S rDNA site patterns and six 18S rDNA site patterns in the 12 diploid species. These rDNA sites occurred in pairs, except for the seven 18S rDNA sites observed in <i>Ipomoea digitata</i>. PCR amplification of 5S rDNA identified four distinct patterns, while 18S rDNA showed only a single pattern across the species. Phylogenetic analysis divided the 13 species into two primary clades, with the closest relationships found between <i>I. batatas</i> and <i>Ipomoea trifida</i>, as well as between <i>Ipomoea platensis</i> and <i>I. digitata</i>. <b>Conclusions:</b> These results enhance our understanding of the diversity among <i>Ipomoea</i> species and provide valuable insights for breeders using these species to generate improved varieties.