Fernández-Pérez Jenyfer, Nantón Ana, Méndez Josefina
Grupo Xenomar, Departamento de Bioloxía, Facultade de Ciencias and Centro de Investigaciones Científicas Avanzadas (CICA), Universidade da Coruña, Campus de A Zapateira, 15071, A Coruña, Spain.
BMC Genet. 2018 Oct 26;19(1):97. doi: 10.1186/s12863-018-0684-x.
The whole repeat unit of 5S rDNA and the internal transcribed spacer (ITS) of four European Donax species were analysed. After amplifying, cloning and sequencing several 5S and ITS units, their basic features and their variation were described. The phylogenetic usefulness of 5S and ITS sequences in the inference of evolutionary relationships among these wedge clams was also investigated.
The length of the 5S repeat presented little variation among species, except D. trunculus that differed from the rest of the Donax species in 170-210 bp. The deduced coding region covered 120 bp, and showed recognizable internal control regions (ICRs) involved in the transcription. The length of non-transcribed spacer region (NTS) ranged from 157 bp to 165 bp in Donax trunculus and from 335 bp to 367 bp in the other three species. The conservation degree of transcriptional regulatory regions was analysed revealing a conserved TATA-like box in the upstream region. Regarding ITS sequences, the four Donax species showed slight size differences among clones due to the variation occurring in the ITS1 and ITS2, except Donax variegatus did not display size differences in the ITS2. The total length of the ITS sequence ranged between 814 and 1014 bp. Resulting phylogenetic trees display that the two ribosomal DNA regions provide well-resolved phylogenies where the four European Donax species form a single clade receiving high support in nodes. The topology obtained with 5S sequences was in agreement with Donax evolutionary relationships inferred from several sequences of different nature in previous studies.
This is not only a basic research work, where new data and new knowledge is provided about Donax species, but also have allowed the authentication of these wedge clams and offers future applications to provide other genetic resources.
对四种欧洲多纳克斯蛤的5S核糖体DNA(rDNA)全重复单元和内转录间隔区(ITS)进行了分析。在对多个5S和ITS单元进行扩增、克隆和测序后,描述了它们的基本特征及其变异情况。还研究了5S和ITS序列在推断这些楔形蛤进化关系方面的系统发育实用性。
5S重复序列的长度在物种间变化不大,除了截形多纳克斯蛤,其与其他多纳克斯蛤物种在170 - 210 bp上存在差异。推导的编码区覆盖120 bp,并显示出参与转录的可识别的内部控制区(ICR)。非转录间隔区(NTS)的长度在截形多纳克斯蛤中为157 bp至165 bp,在其他三个物种中为335 bp至367 bp。对转录调控区的保守程度进行分析,发现在上游区域有一个保守的类TATA框。关于ITS序列,由于ITS1和ITS2中发生的变异,四种多纳克斯蛤物种的克隆之间显示出轻微的大小差异,除了杂色多纳克斯蛤在ITS2中没有显示出大小差异。ITS序列的总长度在814至1014 bp之间。生成的系统发育树显示,这两个核糖体DNA区域提供了分辨率良好的系统发育关系,其中四种欧洲多纳克斯蛤物种形成一个单系分支,在节点处得到高度支持。用5S序列获得的拓扑结构与先前研究中从几个不同性质的序列推断出的多纳克斯蛤进化关系一致。
这不仅是一项基础研究工作,提供了关于多纳克斯蛤物种的新数据和新知识,而且还实现了对这些楔形蛤的鉴定,并为提供其他遗传资源提供了未来应用。