Kopecna Olga, Kubickova Svatava, Cernohorska Halina, Cabelova Katerina, Vahala Jiri, Martinkova Natalia, Rubes Jiri
Department of Genetics and Reproduction, Veterinary Research Institute, Hudcova 70, 621 00, Brno, Czech Republic,
Chromosome Res. 2014 Sep;22(3):277-91. doi: 10.1007/s10577-014-9401-4. Epub 2014 Jan 23.
Satellite sequences present in the centromeric and pericentric regions of chromosomes represent useful source of information. Changes in satellite DNA composition may coincide with the speciation and serve as valuable markers of phylogenetic relationships. Here, we examined satellite DNA clones isolated by laser microdissection of centromeric regions of 38 bovid species and categorized them into three types. Sat I sequences from members of Bovini/Tragelaphini/Boselaphini are similar to the well-documented 1.715 sat I DNA family. Sat I DNA from Caprini/Alcelaphini/Hippotragini/Reduncini/Aepycerotini/Cephalophini/Antilopini/Neotragini/Oreotragini form the second group homologous to the common 1.714 sat I DNA. The analysis of sat II DNAs isolated in our study confirmed conservativeness of these sequences within Bovidae. Newly described centromeric clones from Madoqua kirkii and Strepsiceros strepsiceros were similar in length and repetitive tandem arrangement but showed no similarity to any other satellite DNA in the GenBank database. Phylogenetic analysis of sat I sequences isolated in our study from 38 bovid species enabled the description of relationships at the subfamily and tribal levels. The maximum likelihood and Bayesian inference analyses showed a basal position of sequences from Oreotragini in the subfamily Antilopinae. According to the Bayesian inference analysis based on the indels in a partitioned mixed model, Antilopinae satellite DNA split into two groups with those from Neotragini as a basal tribe, followed by a stepwise, successive branching of Cephalophini, Aepycerotini and Antilopini sequences. In the second group, Reduncini sequences were basal followed by Caprini, Alcelaphini and Hippotragini.
存在于染色体着丝粒和近着丝粒区域的卫星序列是有用的信息来源。卫星DNA组成的变化可能与物种形成同时发生,并作为系统发育关系的有价值标记。在这里,我们检查了通过对38种牛科动物着丝粒区域进行激光显微切割分离得到的卫星DNA克隆,并将它们分为三种类型。牛族/薮羚族/四角羚族成员的Sat I序列与记录充分的1.715 Sat I DNA家族相似。来自山羊族/高角羚族/马羚族/水羚族/黑斑羚族/麂羚族/羚羊族/新小羚族/山羚族的Sat I DNA形成了与常见的1.714 Sat I DNA同源的第二组。我们研究中分离得到的Sat II DNA分析证实了这些序列在牛科动物中的保守性。新描述的来自柯氏犬羚和大羚羊的着丝粒克隆在长度和重复串联排列上相似,但与GenBank数据库中的任何其他卫星DNA都没有相似性。我们对从38种牛科动物中分离得到的Sat I序列进行的系统发育分析,能够描述亚科和族水平上的关系。最大似然法和贝叶斯推断分析表明,山羚族的序列在羚羊亚科中处于基部位置。根据基于分区混合模型中的插入缺失的贝叶斯推断分析,羚羊亚科卫星DNA分为两组,新小羚族的序列作为基部族,随后是麂羚族、黑斑羚族和羚羊族序列的逐步连续分支。在第二组中,水羚族序列是基部的,随后是山羊族、高角羚族和马羚族。