贵州省科学技术基金项目
采用双色荧光原位杂交技术,对栽培荞麦甜荞和苦荞有丝分裂中期染色体上的45S 和5S rDNA基因物理位置进行了定位分析。结果表明,甜荞有4对45S rDNA位点,位于ⅠS、ⅡS、ⅢL、ⅤL(L和S代表长臂和短臂,罗马数字代表染色体序号,下同);2对5S rDNA位点,位于ⅠL、ⅣS;苦荞有5对45S rDNA位点,位于ⅠS、ⅡS、ⅢL、ⅤL、ⅦS;3对5S rDNA位点,位于ⅠL、ⅣS、ⅥS。甜荞与苦荞的45S和5S rDNA位点具有明显的差异,显示其起源上关系较远。依据中期染色体45S 和5S rDNA位点信息及经典核型特征,可以准确鉴别甜荞与苦荞8对同源染色体。
The 45S and 5S rDNA loci were physically mapped by double color fluorescent in situ hybridization (FISH) on the mitotic metaphase chromosomes of F. esculentum and F. tataricum. The results showed four pairs of 45S rDNA loci on ⅠS, ⅡS, ⅢL, and ⅤL (L and S represent chromosome long and short arm respectively, and the Roman number indicate chromosomes serial number, hereinafter the same), as well as two pairs of 5S rDNA loci on ⅠL and ⅣS in F. esculentum, and five pairs of 45S rDNA loci on ⅠS, ⅡS, ⅢL, ⅤL, and ⅦS, as well as three pairs of 5S rDNA loci on ⅠL, ⅣS, and ⅥS in F. tataricum. There are obviously differences in 45S and 5S rDNA loci of F. esculentum and F. tataricum, suggesting they are far in phylogenies. Based on 45S and 5S rDNA loci location and karyotype characteristics of the mitotic metaphase chromosomes, eight pairs of homologous chromosomes of F. esculentum and F. tataricum all can be distinguished distinctly, respectively.
盛茂银.栽培荞麦45S和5S rDNA的染色体物理定位研究[J].植物遗传资源学报,2013,14(2):317-321.
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