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. 2013 Feb 2;54(2):147–155. doi: 10.1007/s13353-013-0133-5

Table 1.

Plant material used for fluorescence in situ hybridization polymorphism analysis

Accession/form Number of plants Genome structure Source
Aegilops umbellulata 20 2n = 2x = 14, UU National Small Grains Germplasm Research Facility, National Small Grains Collection (Aberdeen, Idaho, USA)
Aegilops comosa 20 2n = 2x = 14, MM National Small Grains Germplasm Research Facility, National Small Grains Collection (Aberdeen, Idaho, USA)
Aegilops sharonensis 20 2n = 2x = 14, SshSsh National Small Grains Germplasm Research Facility, National Small Grains Collection (Aberdeen, Idaho, USA)
Aegilops tauschii 20 2n = 2x = 14, DD National Small Grains Germplasm Research Facility, National Small Grains Collection (Aberdeen, Idaho, USA)
Secale cereale n/aa 2n = 2x = 14, RR Institute of Plant Genetics, Polish Academy of Sciences
Aegilops kotschyi 20 2n = 4x = 28, UUSS Weizmann Institute of Science, Rehovot, Israel
Aegilops ovata 20 2n = 4x = 28, UUMM Weizmann Institute of Science, Rehovot, Israel
Aegilops tauschii × Secale cereale 20 2n = 4x = 28, DDRR Institute of Plant Genetics, Polish Academy of Sciences
Aegilops kotschyi × Secale cereale 20 2n = 6x = 42, UUSSRR Institute of Plant Genetics, Polish Academy of Sciences
Aegilops ovata × Secale cereale 20 2n = 6x = 42, UUMMRR Institute of Plant Genetics, Polish Academy of Sciences

aLeaf tissue for DNA isolation