Silva Duílio M Z A, Pansonato-Alves José Carlos, Utsunomia Ricardo, Daniel Sandro Natal, Hashimoto Diogo Teruo, Oliveira Claudio, Porto-Foresti Fabio, Foresti Fausto
Departamento de Morfologia, Instituto de Biociências, Universidade Estadual Paulista, Distrito de Rubião Junior, s/n, Botucatu, SP, 18618-970, Brazil,
Genetica. 2013 Sep;141(7-9):329-36. doi: 10.1007/s10709-013-9732-7. Epub 2013 Sep 6.
Repetitive DNA sequences constitute a great portion of the genome of eukaryotes and are considered key components to comprehend evolutionary mechanisms and karyotypic differentiation. Aiming to contribute to the knowledge of chromosome structure and organization of some repetitive DNA classes in the fish genome, chromosomes of two allopatric populations of Astyanax bockmanni were analyzed using classic cytogenetics techniques and fluorescent in situ hybridization, with probes for ribosomal DNA sequences, histone DNA and transposable elements. These Astyanax populations showed the same diploid number (2n = 50), however with differences in chromosome morphology, distribution of constitutive heterochromatin, and location of 18S rDNA and retroelement Rex3 sites. In contrast, sites for 5S rDNA and H1, H3 and H4 histones showed to be co-located and highly conserved. Our results indicate that dispersion and variability of 18S rDNA and heterochromatin sites are not associated with macro rearrangements in the chromosome structure of these populations. Similarly, distinct evolutionary mechanisms would act upon histone genes and 5S rDNA, contributing to chromosomal association and co-location of these sequences. Data obtained indicate that distinct mechanisms drive the spreading of repetitive DNAs in the genome of A. bockmanni. Also, mobile elements may account for the polymorphism of the major rDNA sites and heterochromatin in this genus.
重复DNA序列构成了真核生物基因组的很大一部分,被认为是理解进化机制和核型分化的关键组成部分。为了有助于了解鱼类基因组中某些重复DNA类别的染色体结构和组织,利用经典细胞遗传学技术和荧光原位杂交,对博氏丽脂鲤两个异域种群的染色体进行了分析,使用了核糖体DNA序列、组蛋白DNA和转座元件的探针。这些丽脂鲤种群显示出相同的二倍体数(2n = 50),然而在染色体形态、组成型异染色质分布以及18S rDNA和反转录元件Rex3位点的位置上存在差异。相比之下,5S rDNA以及H1、H3和H4组蛋白的位点显示是共定位且高度保守的。我们的结果表明,18S rDNA和异染色质位点的分散和变异性与这些种群染色体结构中的宏观重排无关。同样,不同的进化机制作用于组蛋白基因和5S rDNA,促成了这些序列的染色体关联和共定位。获得的数据表明,不同的机制驱动了重复DNA在博氏丽脂鲤基因组中的扩散。此外,移动元件可能是该属主要rDNA位点和异染色质多态性的原因。