Genome. 1997 Oct;40(5):589-93. doi: 10.1139/g97-077.
Using the Aegilops tauschii clone pAs1 together with the barley clone pHvG38 for two-colour fluorescence in situ hybridization (FISH) the entire chromosome complement of hexaploid wheat was identified. The combination of the two probes allowed easy discrimination of the three genomes of wheat. The banding pattern obtained with the pHvG38 probe containing the GAA-satellite sequence was identical to the N-banding pattern of wheat. A detailed idiogram was constructed, including 73 GAA bands and 48 pAs1 bands. Identification of the wheat chromosomes by FISH will be particularly useful in connection with the physical mapping of other DNA sequences to chromosomes, or for chromosome identification in general, as an alternative to C-banding.
使用 Aegilops tauschii 克隆 pAs1 与大麦克隆 pHvG38 进行双色荧光原位杂交 (FISH),鉴定了六倍体小麦的整个染色体组。这两个探针的组合使得很容易区分小麦的三个基因组。用包含 GAA 卫星序列的 pHvG38 探针获得的带型与小麦的 N 带型相同。构建了一个详细的染色体图,包括 73 个 GAA 带和 48 个 pAs1 带。通过 FISH 鉴定小麦染色体对于将其他 DNA 序列物理图谱定位到染色体上,或者对于一般的染色体鉴定,作为 C-带的替代方法,将特别有用。