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Mapping of rRNA genes and telomeric sequences in Danube salmon (Hucho hucho) chromosomes using primed in situ labeling technique (PRINS)

机译:使用引物原位标记技术(PRINS)在多瑙河鲑(Hucho hucho)染色体中绘制rRNA基因和端粒序列

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In the current paper we described the application of primed in situ (PRINS) labeling approach for the chromosomal mapping of repetitive DNA sequences in Danube salmon (Hucho hucho) (2n = 82, NF = 112). PRINS was successfully performed with primers enabling amplification of 5S rRNA genes (minor rDNAs), NOR building DNA sequences (major rDNAs), and telomeric sequences. Two loci of 5S rRNA were observed on distinct chromosome pairs; the minor arrays were located interstitially on the long (q) arms of two large metacentrics (chromosomes No. 3) and the large clusters of 5S rDNAs were assigned to the short (p) arms of two subtelocentric chromosomes No. 18. Major rDNA clusters were observed on the p-arms of two submeta-subtelocentric chromosomes No. 10. These chromosomal areas were built with GC-rich chromatin what was proved in the course of chromomycin A3 (CMA3) staining performed sequentially. Major and minor rDNA families were not co-localized in the Danube salmon chromosomes.The distinct hybridization signals at the ends of all the chromosomes were provided in the course of PRINS with (CCCTAA) n primer. The chromosomal localization of rRNA genes and telomeric DNA sequences was discussed in the context of Salmonidae karyotype evolution.
机译:在当前的论文中,我们描述了原位标记(PRINS)标记方法在多瑙河鲑鱼(Hucho hucho)(2n = 82,NF = 112)中重复DNA序列的染色体作图的应用。 PRINS用引物成功进行,能够扩增5S rRNA基因(次要rDNA),NOR构建DNA序列(主要rDNA)和端粒序列。在不同的染色体对上观察到两个5S rRNA基因座。次要阵列位于两个大的超中心点(3号染色体)的长(q)臂间,而5S rDNA的大簇被分配给两个18号亚远心染色体的短臂(p)。在两个亚元-亚近端染色体第10号的p臂上观察到了这些染色体区域。这些区域是用富含GC的染色质构建的,染色质A 3 (CMA 3 )染色顺序进行。主要和次要rDNA家族不在多瑙河鲑鱼染色体中共定位。在所有染色体末端的独特杂交信号是在PRINS过程中使用(CCCTAA) n 引物提供的。在鲑鱼核型进化的背景下讨论了rRNA基因和端粒DNA序列的染色体定位。

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