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通过染色体显带和荧光原位杂交对麝香百合和玫红百合进行核型分析。

Karyotype analysis of Lilium longiflorum and Lilium rubellum by chromosome banding and fluorescence in situ hybridisation.

作者信息

Lim K B, Wennekes J, de Jong J H, Jacobsen E, van Tuyl J M

机构信息

Plant Research International, Business Unit Genetics and Breeding, Wageningen, The Netherlands.

出版信息

Genome. 2001 Oct;44(5):911-8.

Abstract

Detailed karyotypes of Lilium longiflorum and L. rubellum were constructed on the basis of chromosome arm lengths, C-banding, AgNO3 staining, and PI-DAPI banding, together with fluorescence in situ hybridisation (FISH) with the 5S and 45S rDNA sequences as probes. The C-banding patterns that were obtained with the standard BSG technique revealed only few minor bands on heterologous positions of the L. longiflorum and L. rubellum chromosomes. FISH of the 5S and 45S rDNA probes on L. longiflorum metaphase complements showed overlapping signals at proximal positions of the short arms of chromosomes 4 and 7, a single 5S rDNA signal on the secondary constriction of chromosome 3, and one 45S rDNA signal adjacent to the 5S rDNA signal on the subdistal part of the long arm of chromosome 3. In L. rubellum, we observed co-localisation of the 5S and 45S rDNA sequences on the short arm of chromosomes 2 and 4 and on the long arms of chromosomes 2 and 3, and two adjacent bands on chromosome 12. Silver staining (Ag-NOR) of the nucleoli and NORs in L. longiflorum and L. rubellum yielded a highly variable number of signals in interphase nuclei and only a few faint silver deposits on the NORs of mitotic metaphase chromosomes. In preparations stained with PI and DAPI, we observed both red- and blue-fluorescing bands at different positions on the L. longiflorum and L. rubellum chromosomes. The red-fluorescing or so-called reverse PI-DAPI bands always coincided with rDNA sites, whereas the blue-fluorescing DAPI bands corresponded to C-bands. Based on these techniques, we could identify most of chromosomes of the L. longiflorum and L. rubellum karyotypes.

摘要

基于染色体臂长、C 带、硝酸银染色和 PI-DAPI 带型,并结合以 5S 和 45S rDNA 序列为探针的荧光原位杂交(FISH)技术,构建了麝香百合和玫红百合的详细核型。采用标准 BSG 技术获得的 C 带模式显示,麝香百合和玫红百合染色体的异源位置上只有少数次要带。5S 和 45S rDNA 探针在麝香百合中期染色体组上的 FISH 结果显示,在 4 号和 7 号染色体短臂的近端位置有重叠信号,在 3 号染色体的次缢痕处有一个单一的 5S rDNA 信号,在 3 号染色体长臂亚远端部分与 5S rDNA 信号相邻处有一个 45S rDNA 信号。在玫红百合中,我们观察到 5S 和 45S rDNA 序列在 2 号和 4 号染色体短臂以及 2 号和 3 号染色体长臂上共定位,并且在 12 号染色体上有两条相邻带。麝香百合和玫红百合核仁及核仁组织区(NOR)的银染(Ag-NOR)在间期核中产生了数量高度可变的信号,而在有丝分裂中期染色体的 NOR 上只有少数微弱的银沉积。在用 PI 和 DAPI 染色的制片中,我们在麝香百合和玫红百合染色体的不同位置观察到了红色和蓝色荧光带。红色荧光或所谓的反向 PI-DAPI 带总是与 rDNA 位点重合,而蓝色荧光的 DAPI 带对应于 C 带。基于这些技术,我们能够识别麝香百合和玫红百合核型中的大多数染色体。

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