Caputo V, Giovannotti M, Nisi Cerioni P, Splendiani A, Olmo E
Istituto di Biologia e Genetica, Università Politecnica delle Marche, Ancona, Italy.
Cytogenet Genome Res. 2009;124(1):51-62. doi: 10.1159/000200088. Epub 2009 Apr 15.
A cytogenetic analysis was carried out using conventional staining, banding techniques and fluorescence in situ hybridization (FISH) in Italian populations of brown trout (Salmo truttacomplex). All individuals analysed, belonging to the Atlantic (At), Marmoratus (Ma), Adriatic (Ad) and Mediterranean (Me) lineages, showed remarkable karyotype uniformity, with diploid complement of 2n = 80 chromosomes, arm number (NF) of 102 and invariable karyotype composition. Such uniformity was also observed with respect to the location of 5S rDNA and the active, i.e. silver-positive NOR sites. On the contrary, FISH with 28S ribosomal probe and fluorescent staining with CMA3 revealed that inactive NOR sites are more numerous in Ad and Me than in At and Ma lineages. A centromeric sequence was successfully isolated from Salmo trutta individuals by polymerase chain reaction (PCR)-based cloning, using primers designed from published Atlantic salmon (Salmo salar) satellite DNA sequences. This sequence had high AT content (65.3%) and short consensus motif (A/T)(G/C)AAA(T/C) similar to other centromeric satellite repeats. The isolated satellite DNA clones were localized with FISH in the centromeric regions of the brown trout chromosomes, showing lineage-specific patterns. Because it is well known that AT-rich sequences can induce a pronounced DNA curvature, which in turn would promote faster and higher chromatin spiralization, it may be hypothesised that the wide distribution of this satellite in the S. trutta genome may have played a role in its karyotype stability. The presence of this sequence in other salmonid species was also tested by Southern blot hybridization and used to analyze its evolution within salmonids.
利用常规染色、显带技术和荧光原位杂交(FISH)对意大利褐鳟(Salmo trutta complex)种群进行了细胞遗传学分析。所有分析的个体,属于大西洋(At)、大理石纹(Ma)、亚得里亚海(Ad)和地中海(Me)谱系,均显示出显著的核型一致性,二倍体染色体数为2n = 80条,臂数(NF)为102,核型组成不变。在5S rDNA的位置以及活跃的(即银染阳性的)核仁组织区(NOR)位点方面也观察到了这种一致性。相反,用28S核糖体探针进行FISH以及用CMA3进行荧光染色显示,Ad和Me谱系中不活跃NOR位点的数量比At和Ma谱系中的更多。通过基于聚合酶链反应(PCR)的克隆,使用从已发表的大西洋鲑(Salmo salar)卫星DNA序列设计的引物,成功从褐鳟个体中分离出一个着丝粒序列。该序列的AT含量高(65.3%),具有短的共有基序(A/T)(G/C)AAA(T/C),与其他着丝粒卫星重复序列相似。分离出的卫星DNA克隆通过FISH定位在褐鳟染色体的着丝粒区域,显示出谱系特异性模式。由于众所周知富含AT的序列可诱导明显的DNA弯曲,进而促进更快、更高程度的染色质螺旋化,因此可以推测该卫星在褐鳟基因组中的广泛分布可能在其核型稳定性中发挥了作用。还通过Southern印迹杂交检测了该序列在其他鲑科物种中的存在情况,并用于分析其在鲑科鱼类中的进化。