| Literature DB >> 33643358 |
Nomar Espinosa Waminal1, Remnyl Joyce Pellerin1, Sang-Ho Kang2, Hyun Hee Kim1.
Abstract
Tandem repeats can occupy a large portion of plant genomes and can either cause or result from chromosomal rearrangements, which are important drivers of dysploidy-mediated karyotype evolution and speciation. To understand the contribution of tandem repeats in shaping the extant Senna tora dysploid karyotype, we analyzed the composition and abundance of tandem repeats in the S. tora genome and compared the chromosomal distribution of these repeats between S. tora and a closely related euploid, Senna occidentalis. Using a read clustering algorithm, we identified the major S. tora tandem repeats and visualized their chromosomal distribution by fluorescence in situ hybridization. We identified eight independent repeats covering ~85 Mb or ~12% of the S. tora genome. The unit lengths and copy numbers had ranges of 7-5,833 bp and 325-2.89 × 106, respectively. Three short duplicated sequences were found in the 45S rDNA intergenic spacer, one of which was also detected at an extra-NOR locus. The canonical plant telomeric repeat (TTTAGGG)n was also detected as very intense signals in numerous pericentromeric and interstitial loci. StoTR05_180, which showed subtelomeric distribution in Senna occidentalis, was predominantly pericentromeric in S. tora. The unusual chromosomal distribution of tandem repeats in S. tora not only enabled easy identification of individual chromosomes but also revealed the massive chromosomal rearrangements that have likely played important roles in shaping its dysploid karyotype.Entities:
Keywords: Senna tora; dysploidy; fluorescence in situ hybridization; karyotype; satellite DNA; tandem repeats; whole genome duplication
Year: 2021 PMID: 33643358 PMCID: PMC7902697 DOI: 10.3389/fpls.2021.629898
Source DB: PubMed Journal: Front Plant Sci ISSN: 1664-462X Impact factor: 5.753