|
Plant | Chromosome number | Genomic DNA | Blocking DNA | Working | Reference |
|
Fruit |
Cherry | 2n = 16 | P. avium/P. fruticosa | P. fruticosa/P. avium | Genomic evaluation | [30] |
Citrus | 2n = 18 | C. reticulata (dig labeled) | C. maxima (biotin labeled) | Karyotype analysis of chromosomes | [17] |
Diospyros | 2n = 30 | D. kaki + D. glandulosa | No blocking DNA | Multicolor GISH study of somatic hybrid chromosomes | [18] |
Mango | 2n = 40 | M. caloneura/M. cochinchinensis/M. flava/M. gracilipes/M. griffithii/M. sylvatica/M. indica/M. foetida/M. macrocarpa | No blocking DNA | Phylogenetic division using karyotype tool | [30] |
Vegetable |
Onion | 2n = 40 | A. galanthum | A. fistulosum | Gene identification on chromosomal regions | [19] |
2n = 40 | A. roylei | A. cepa | Karyotype study and hybridity status in F1 hybrids | [41] |
2n = 40 | A. fistulosum | A. cepa | Genomic analysis of advanced interspecfic generations with relative resistance to downy mildew | [62] |
Onion & garlic | 2n = 40 | A. sativum (garlic) | A. cepa (onion) | Chromosome evaluation in onion and garlic somatic hybridization | [35] |
Potato | 2n = 24 | S. verrucosum, S. hougasii, S. andreanum | S. jamesii | Auto and allopolyploid genomic origin in potato species | [29] |
Tomato | 2n = 24 | L. esculentum/S. lycopersicoides/S. sitiens | L. esculentum/S. lycopersicoides/S. sitiens | Genomic discrimination in interspecific and intergeneric hybrids | [40] |
Tomato & potato | 2n = 24 | L. pennellii (tomato) | S. tuberosum (potato) | Genomic analysis of trigenomic hybrids | [38] |
Ornamental |
Begonia | 2n = 28 | Tuberous Begonia | B. socotrana | Genomic constituents of begonia hybrids | [39] |
Clivia | 2n = 22 | C. nobilis/C. caulescens/C. gardenii/C. miniata | C. nobilis/C. caulescens/C. gardenii/C. miniata | Hybrid confirmation | [48] |
Festulolium (Festuca × Lolium) | 2n = 4x = 28 | Lolium multiflorum/Festuca pratensis | No blocking DNA | Genomic constitution determination in hybrids | [63] |
Lycoris | 2n = 14–22 | L. aurea/L. radiata | L. aurea/L. radiata | Chromosome complements variation in interspecific hybrids | [51] |
Orchids | 2n = 38 | P. aphrodite/P. sanderiana/P. mannii/P. vialacea/P. ambainensis/P. stuartiana | P. aphrodite/P. sanderiana/P. mannii/P. vialacea/P. ambainensis/P. stuartiana | Genomic composition and species relationship by genomic analysis | [64] |
2n = 26 | P. delenatii/P. rothschildianum | P. delenatii/P. rothschildianum | Phylogenetic classification on the basis of chromosome pairing resemblance | [55] |
Grass (Poa jemtlandica, Poa flexuosa, Poa alpina) | 2n = 38 2n = 42 2n = 32 | Poa jemtlandica/Poa alpina/Poa flexuosa | Poa alpina/Poa flexuosa | Genome composition and hybrid origin confirmation | [65] |
Primula egaliksensis | 2n = 40 | Primula mistassinica, Primula nutans | Salmon sperm DNA | Genomic composition and evolution of allopolyploid | [66] |
Rhododendron | 2n = 26 | R. aureum, R. brachycarpum, R. catawbiense “Catharine van Tol,” R. yakushimanum | R. aureum, R. catawbiense “Nova Zembla,” R. yakushimanum | Paternity description of interspecific hybrids | [50] |
Tulipa | 2n = 24 | T. fosteriana, T. gesneriana | T. tarda | Genomic recombination in three generations (F1, BC1, and BC2) | [59] |
T. gesneriana and T. fosteriana | Darwin hybrid “Yellow Dover” counter stained with DAPI | Origin investigation by karyotype genomic method | [36] |
T. gesneriana and T. fosteriana | T. sacstatila | Genomic information of interspecific hybrids | [43] |
Lilium | 2n = 24 | Sorbonne and L. regale | Herring sperm | Introgression determination in interpoloid hybrids | [57] |
Oriental/Asiatic/Martagon | Oriental/Asiatic | Backcross progeny analysis | [60] |
L. longiflorum “Snow queen” | Herring sperm | L. rubellum Baker introgression into L. longiflorum Thunb. | [67] |
L. longiflorum | Herring sperm | Genomic evaluation of backcross progenies | [68] |
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