National Engineering Laboratory of Marine Germplasm Resources Exploration and Utilization, Marine Science and Technology College, Zhejiang Ocean University, 316022, Zhoushan, China; Guangxi Key Laboratory of Marine Natural Products and Combinatorial Biosynthesis Chemistry, Guangxi Beibu Gulf Marine Research Center, Guangxi Academy of Sciences, Nanning, 530007, China.
Key Laboratory of Tropical Marine Bio-resources and Ecology, Guangdong Provincial Key Laboratory of Applied Marine Biology, South China Sea Institute of Oceanology, Chinese Academy of Sciences, China.
Biochem Biophys Res Commun. 2021 Jan 1;534:233-239. doi: 10.1016/j.bbrc.2020.11.106. Epub 2020 Dec 1.
Many early studies of ribosomal RNA gene (rDNA) suggested that rDNA tandem repeats within species are homogeneous. However, increasing number of reports have found intra-individual rDNA polymorphism across a range of taxa. Here, we reported a high level of intra-individual polymorphism of 18S-ITS1-5.8S rDNA in the genome of Cynoglossus melampetalus (Pleuronectiformes: Cynoglossidae), indicating a non-concerted evolution manner. Sequence alignments found two distinct types of 18S and 5.8S (Type A and B) and five types of ITS1 sequence (Type A - E) coexisted in the genome differing in length, GC content, secondary structure stability and minimum free energy. Based on the unique features of pseudogene and comparison of the conserved 18S rDNA sequence and 5.8S secondary structure of 22 flatfishes revealed that Type B sequences of 18S, 5.8S and their linked ITS1 were putative pseudogenes. So far, detection of rRNA pseudogenes from the multiple rDNA copies has been an intricate puzzle. Our results, as a result, provide a new ideal for rRNA pseudogene identification.
许多早期的核糖体 RNA 基因(rDNA)研究表明,种内的 rDNA 串联重复是同质的。然而,越来越多的报告发现,在一系列分类群中存在个体内 rDNA 多态性。在这里,我们报道了圆斑星鲽(鲽形目:舌鳎科)基因组中 18S-ITS1-5.8S rDNA 高水平的个体内多态性,表明其进化方式是非协同的。序列比对发现,两种不同类型的 18S 和 5.8S(A 型和 B 型)和五种类型的 ITS1 序列(A-E 型)共存于基因组中,其长度、GC 含量、二级结构稳定性和最小自由能存在差异。基于假基因的独特特征以及对 22 种比目鱼保守的 18S rDNA 序列和 5.8S 二级结构的比较,18S、5.8S 的 B 型序列及其连接的 ITS1 被认为是假定的假基因。到目前为止,从多个 rDNA 拷贝中检测 rRNA 假基因一直是一个复杂的难题。我们的结果为 rRNA 假基因的鉴定提供了一个新的理想方法。