Molecular cytogenetic characterization and phylogenetic analysis of four Miscanthus species (Poaceae)

• Published in: Comparative cytogenetics Vol. 13; no. 3; pp. 211 - 230
• Main Authors: Tang, Yan-Mei, Xiao, Liang, Iqbal, Yasir, Liao, Jian-Feng, Xiao, Long-Qian, Yi, Zi-Li, She, Chao-Wen
• Format: Journal Article
• Language: English
• Published: Bulgaria Pensoft Publishers 09.08.2019
• Subjects: 4',6-diamidino-2-phenylindole; Asia; Cenozoic; Chromosomes; Cytogenetics; Deoxyribonucleic acid; DNA; fish; Fluorescence; Fluorescence in situ hybridization; Genetics; Genomic in situ hybridization; Genomics; Homology; Hybridization; internal transcribed spacers; Karyotypes; karyotyping; Miscanthus; Miscanthus floridulus; Molecular Cytogenetics; Phylogenetics; Phylogeny; Plantae; Spacer; Species; Staining; internal transcribed spacers; karyotype; Miscanthus; fluorochrome banding; phylogeny; 45S ribosomal RNA genes (45S rDNA); in situ hybridization
• ISSN: 1993-0771; 1993-078X; 1993-078X
• DOI: 10.3897/CompCytogen.v13i3.35346

Chromosomes of four Miscanthus (Andersson, 1855) species including M. sinensis (Andersson, 1855), M. floridulus (Schumann & Lauterb, 1901), M. sacchariflorus (Hackel, 1882) and M. lutarioriparius (Chen & Renvoize, 2005) were analyzed using sequentially combined PI and DAPI (CPD) staining and fluorescence in situ hybridization (FISH) with 45S rDNA probe. To elucidate the phylogenetic relationship among the four Miscanthus species, the homology of repetitive sequences among the four species was analyzed by comparative genomic in situ hybridization (cGISH). Subsequently four Miscanthus species were clustered based on the internal transcribed spacer (ITS) of 45S rDNA. Molecular cytogenetic karyotypes of the four Miscanthus species were established for the first time using chromosome measurements, fluorochrome bands and 45S rDNA FISH signals, which will provide a cytogenetic tool for the identification of these four species. All the four have the karyotype formula of Miscanthus species, which is 2n = 2x = 38 = 34m(2SAT) + 4sm, and one pair of 45S rDNA sites. The latter were shown as strong red bands by CPD staining. A non-rDNA CPD band emerged in M. floridulus and some blue DAPI bands appeared in M. sinensis and M. floridulus . The hybridization signals of M. floridulus genomic DNA to the chromosomes of M. sinensis and M. lutarioriparius genomic DNA to the chromosomes of M. sacchariflorus were stronger and more evenly distributed than other combinations. Molecular phylogenetic trees showed that M. sinensis and M. floridulus were closest relatives, and M. sacchariflorus and M. lutarioriparius were also closely related. These findings were consistent with the phylogenetic relationships inferred from the cGISH patterns.