Gouveia Juceli Gonzalez, Wolf Ivan Rodrigo, de Moraes-Manécolo Vivian Patrícia Oliveira, Bardella Vanessa Belline, Ferracin Lara Munique, Giuliano-Caetano Lucia, da Rosa Renata, Dias Ana Lúcia
Departamento de Biologia Geral, Centro de Ciências Biológicas, CCB, Universidade Estadual de Londrina, P.O Box 6001, Londrina, Paraná, CEP 86051-970, Brazil.
Cytotechnology. 2016 Dec;68(6):2711-2720. doi: 10.1007/s10616-016-9996-8. Epub 2016 Jun 25.
Sequences of 5S ribosomal RNA (rRNA) are extensively used in fish cytogenomic studies, once they have a flexible organization at the chromosomal level, showing inter- and intra-specific variation in number and position in karyotypes. Sequences from the genome of Imparfinis schubarti (Heptapteridae) were isolated, aiming to understand the organization of 5S rDNA families in the fish genome. The isolation of 5S rDNA from the genome of I. schubarti was carried out by reassociation kinetics (Ct) and PCR amplification. The obtained sequences were cloned for the construction of a micro-library. The obtained clones were sequenced and hybridized in I. schubarti and Microglanis cottoides (Pseudopimelodidae) for chromosome mapping. An analysis of the sequence alignments with other fish groups was accomplished. Both methods were effective when using 5S rDNA for hybridization in I. schubarti genome. However, the Ct method enabled the use of a complete 5S rRNA gene, which was also successful in the hybridization of M. cottoides. Nevertheless, this gene was obtained only partially by PCR. The hybridization results and sequence analyses showed that intact 5S regions are more appropriate for the probe operation, due to conserved structure and motifs. This study contributes to a better understanding of the organization of multigene families in catfish's genomes.
5S核糖体RNA(rRNA)序列在鱼类细胞基因组研究中被广泛应用,因为它们在染色体水平上具有灵活的组织形式,在核型中的数量和位置表现出种间和种内变异。本研究分离了舒氏异鳍脂鲤(Imparfinis schubarti,项鳍鲶科)基因组中的序列,旨在了解鱼类基因组中5S rDNA家族的组织情况。通过复性动力学(Ct)和PCR扩增从舒氏异鳍脂鲤基因组中分离5S rDNA。将获得的序列克隆以构建微文库。对获得的克隆进行测序,并在舒氏异鳍脂鲤和科氏小陶乐鲶(Microglanis cottoides,拟油鲶科)中进行杂交以进行染色体定位。完成了与其他鱼类群体的序列比对分析。在舒氏异鳍脂鲤基因组中使用5S rDNA进行杂交时,这两种方法都有效。然而,Ct方法能够使用完整的5S rRNA基因,该基因在科氏小陶乐鲶的杂交中也取得了成功。不过,通过PCR仅部分获得了该基因。杂交结果和序列分析表明,由于结构和基序保守,完整的5S区域更适合用于探针操作。本研究有助于更好地理解鲶鱼基因组中多基因家族的组织情况。