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Chromosomal characteristics and distribution of rDNA sequences in the brook trout Salvelinus fontinalis (Mitchill 1814)

机译:溪鳟Salvelinus fontinalis中的rDNA的染色体特征和分布(Mitchill1814)

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摘要

Brook trout Salvelinus fontinalis (Mitchill, 1814) chromosomes have been analyzed using conventional and molecular cytogenetic techniques enabling characteristics and chromosomal location of heterochromatin, nucleolus organizer regions (NORs), ribosomal RNA-encoding genes and telomeric DNA sequences. The C-banding and chromosome digestion with the restriction endonucleases demonstrated distribution and heterogeneity of the heterochromatin in the brook trout genome. DNA sequences of the ribosomal RNA genes, namely the nucleolus-forming 28S (major) and non-nucleolus-forming 5S (minor) rDNAs, were physically mapped using fluorescence in situ hybridization (FISH) and primed in situ labelling. The minor rDNA locus was located on the subtelo-acrocentric chromosome pair No. 9, whereas the major rDNA loci were dispersed on 14 chromosome pairs, showing a considerable inter-individual variation in the number and location. The major and minor rDNA loci were located at different chromosomes. Multichromosomal location (3–6 sites) of the NORs was demonstrated by silver nitrate (AgNO3) impregnation. All Ag-positive i.e. active NORs corresponded to the GC-rich blocks of heterochromatin. FISH with telomeric probe showed the presence of the interstitial telomeric site (ITS) adjacent to the NOR/28S rDNA site on the chromosome 11. This ITS was presumably remnant of the chromosome rearrangement(s) leading to the genomic redistribution of the rDNA sequences. Comparative analysis of the cytogenetic data among several related salmonid species confirmed huge variation in the number and the chromosomal location of rRNA gene clusters in the Salvelinus genome.
机译:已使用常规和分子细胞遗传学技术分析了布鲁克鳟鱼Salvelinus fontinalis(Mitchill,1814)的染色体,这些技术能够实现异染色质,核仁组织区(NORs),核糖体RNA编码基因和端粒DNA序列的特征和染色体位置。 C条带和限制性内切酶的染色体消化证明了杂种染色质在溪鳟基因组中的分布和异质性。核糖体RNA基因的DNA序列,即形成核仁的28S(主要)和非形成核仁的5S(次要)rDNA,使用荧光原位杂交(FISH)进行了物理定位,并进行了原位标记。较小的rDNA基因座位于9号亚端-近端染色体上,而主要的rDNA基因座则分散在14对染色体上,显示出个体和数量上的巨大差异。主要和次要rDNA基因座位于不同的染色体上。硝酸银(AgNO3)的浸渍证明了NORs的多染色体位置(3–6个位点)。所有的Ag阳性即活性NORs对应于富含GC的异染色质嵌段。带有端粒探针的FISH显示在11号染色体上与NOR / 28S rDNA位点相邻的间质端粒位点(ITS)的存在。该ITS可能是染色体重排的残余,导致rDNA序列的基因组重新分布。对几种相关鲑科物种的细胞遗传学数据进行比较分析,证实了Salvelinus基因组中rRNA基因簇的数量和染色体位置存在巨大差异。

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