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FISH analysis of Zanthoxylum armatum based on oligonucleotides for 5S rDNA and (GAA)6

机译:基于寡核苷酸的Zanthoxylum Armatum的鱼分析5S rDNA和(Gaa)6

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Fluorescence in situ hybridization (FISH) using oligonucleotide probes for (GAA)6 (18 bp) and ribosomal DNA (rDNA) (5S rDNA, 41 bp) was applied to analyse Zanthoxylum armatum. (GAA)6 loci were detected on the pericentromeric regions of five chromosome pairs, and 5S rDNA loci were also detected on the pericentromeric regions of another two chromosome pairs. The densities and locations of (GAA)6 and 5S rDNA signals varied between individual chromosomes. High-intensity (GAA)6 signals were detected at the centromeres of two large and two smaller metacentric chromosomes. Relatively strong (GAA)6 signals were detected at the centromeres of two relatively small metacentric chromosomes, although strong 5S rDNA signals were detected at the centromeres of two additional smaller metacentric chromosomes. Weak (GAA)6 signals were detected at the centromeres of four large metacentric chromosomes, whereas weak 5S rDNA signals were detected at the centromeres of two smaller metacentric chromosomes. The remaining chromosomes exhibited no signals. Zanthoxylum armatum had 2n = ~128. The lengths of the mitotic metaphase chromosomes ranged from 1.22 to 2.34 μm. Our results provide information that may be beneficial for future cytogenetic studies and could contribute to the physical assembly of the Zanthoxylum genome.
机译:使用寡核苷酸探针(Gaa)6(18bp)和核糖体DNA(RDNA)(5S rDNA)(5s RDNA,41bp)的荧光用于分析Zanthoxylum Armatum。 (Gaa)6在五种染色体对的蠕虫熵区域上检测到基因座,并且还在另外两种染色体对的蠕虫熵区域上检测到5S rdNA基因座。 (Gaa)6和5s rdNA信号的密度和位置在各个染色体之间变化。在两个大和两个较小的染色体的焦点上检测高强度(Gaa)6信号。在两个相对较小的核心染色体的焦点上检测到相对较强的(GaA)6信号,但在两种额外的较小染色体的焦点下检测强5S rdNA信号。在四个大型染色体的焦点上检测到薄弱(GaA)6信号,而在两个较小的核心染色体的焦粒子中检测到弱5S rdNA信号。剩余的染色体没有信号。 Zanthoxylum Armatum有2n =〜128。有丝分裂中期染色体的长度范围为1.22至2.34μm。我们的结果提供了对未来细胞遗传学研究可能有益的信息,并且可以有助于Zanthoxylum基因组的物理组装。

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