Morescalchi Maria Alessandra, Stingo Vincenzo, Capriglione Teresa
Dipartimento di Scienze della Vita, Seconda Università degli Studi di Napoli, via Vivaldi 43, 81100 Caserta, Italy.
Mar Genomics. 2011 Mar;4(1):25-31. doi: 10.1016/j.margen.2010.12.002. Epub 2011 Jan 21.
Polypteridae is a family of archaic freshwater African fish that constitute an interesting subject for the study of the karyological evolution in vertebrates, on account of their primitive morphological characters and peculiar relationships with lower Osteichthyans. In this paper, a cytogenetic analysis on twenty specimens of both sexes of Polypterus ornatipinnis the ornate "bichir", coming from the Congo River basin, was performed by using both classical and molecular techniques. The karyotypic formula (2n=36; FN=72) was composed of 26 M+10 SM. The Alu I banding, performed to characterize heterochromatin in this species, was mainly centromeric. Both the chromosome location of the ribosomal 5S and 18S rRNA genes were examined by using Ag-NOR, classical C-banding, CMA(3) staining and FISH. CMA(3) marked all centromerical regions and showed the presence of two GC rich regions on the p arm of the chromosome pair n°1 and on the q arm of the pair n°14. Staining with Ag-NOR marked the only telomeric region of the chromosome n°1 p arm. After PCR, the 5S rDNA in this species was cloned, sequenced and analyzed. In the 665bp 5S rDNA sequence of P.ornatipinnis, a conserved 120bp gene region for the 5S rDNA was identified, followed by a non-transcribed variable spacer (NTS) which included simple repeats, microsatellites and a fragment of a non-LTR retrotransposon R-TEX. FISH with 5S rDNA marked the subtelomeric region of the q arm of the chromosome pair n°14, previously marked by CMA(3). FISH with 18S rDNA marked the telomeric region of the p arm of the pair n°1, previously marked both by Ag-NOR and CMA(3). The (GATA)(7) repeats marked the telomeric regions of all chromosome pairs, with the exclusion of the n°1, n°3 and n°14; hybridization with telomeric probes (TTAGGG)(n) showed signals at the end of all chromosomes. Karyotype evolution in Polypterus genus was finally discussed, including the new data obtained.
多鳍鱼科是非洲古老的淡水鱼家族,由于其原始的形态特征以及与低等硬骨鱼的特殊关系,成为脊椎动物核型进化研究的一个有趣课题。本文运用经典和分子技术,对20条来自刚果河流域的华丽“恐龙鱼”(Polypterus ornatipinnis)雌雄标本进行了细胞遗传学分析。核型公式(2n = 36;FN = 72)由26条中着丝粒染色体(M)+ 10条亚中着丝粒染色体(SM)组成。为了表征该物种的异染色质而进行的Alu I显带,主要位于着丝粒区域。通过银染核仁组织区(Ag-NOR)、经典C显带、CMA(3)染色和荧光原位杂交(FISH)等方法,对核糖体5S和18S rRNA基因的染色体定位进行了检测。CMA(3)标记了所有着丝粒区域,并显示在第1号染色体对的p臂和第14号染色体对的q臂上存在两个富含GC的区域。Ag-NOR染色标记了第1号染色体p臂上唯一的端粒区域。经过聚合酶链式反应(PCR)后,对该物种的5S rDNA进行了克隆、测序和分析。在华丽多鳍鱼665bp的5S rDNA序列中,鉴定出一个120bp的5S rDNA保守基因区域,随后是一个非转录可变间隔区(NTS),其中包括简单重复序列、微卫星和一个非长末端重复逆转座子R-TEX的片段。用5S rDNA进行荧光原位杂交标记了第14号染色体对q臂的亚端粒区域,该区域先前已被CMA(3)标记。用18S rDNA进行荧光原位杂交标记了第1号染色体对p臂的端粒区域,该区域先前已被Ag-NOR和CMA(3)标记。(GATA)(7)重复序列标记了除第1、3和14号染色体对之外的所有染色体对的端粒区域;与端粒探针(TTAGGG)(n)杂交在所有染色体末端均显示出信号。最后讨论了多鳍鱼属的核型进化,包括所获得的新数据。