4.5 Article

Comparative Analysis of the nrDNA Repeat Unit of Manila Clam Ruditapes philippinarum and Quahog Mercenaria mercenaria

期刊

FISHES
卷 6, 期 3, 页码 -

出版社

MDPI
DOI: 10.3390/fishes6030042

关键词

ribosomal DNA; Ruditapes philippinarum; Mercenaria mercenaria; intergenic spacer; functional element

资金

  1. Fundamental Research Funds for the Central Universities [2019ZRJC006]

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The study obtained the complete ribosomal DNA unit sequences of Ruditapes philippinarum and Mercenaria mercenaria for the first time, revealing genetic differences mainly in non-coding regions between them, and confirming the boundaries of certain unit structures.
Ruditapes philippinarum and Mercenaria mercenaria are economically important bivalve species. The complete ribosomal DNA (rDNA) unit sequences of R. philippinarum and M. mercenaria, with as-sembled rDNA unit lengths of 12,910 and 12,100 bp, respectively, were obtained in this study for the first time. The rDNA unit structural organisation was similar to that in other eukaryotes, in-cluding the following elements in order: 18S rRNA-internal transcribed spacer 1 (ITS1); 5.8S rRNA-ITS2-28S rRNA-intergenic spacer (IGS) (3 ' external transcribed spacer (ETS); non-transcribed spacer (NTS)-5 ' ETS). The genetic differences between R. philippinarum and M. mercenaria were mainly attributable to non-coding regions (ITS1, ITS2 and IGS), especially the IGS region. The boundaries of putative 3 ' ETS, NTS and 5 ' ETS were confirmed. Seven and three sub-repeat fragments were found in R. philippinarum and M. mercenaria, respectively. These frag-ments ranged from 4 to 154 bp in length, and were located at the NTS and 5 ' ETS regions. Five and six cytosine-guanine (CpG) islands were detected in R. philippinarum and M. mercenaria, respec-tively, and these covered 85.58% and 79.29% of the entire IGS sequence, respectively. The phylo-genetic tree was constructed based on Veneridae ITS and 18S rRNA sequences using the maxi-mum likelihood (ML) method. The ML tree based on ITS revealed that species within the same genus clearly clustered together with relatively high supporting values, and all the genera were recovered as monophyletic. The phylogenetic analyses using 18S rRNA provided a weaker phy-logenetic signal than ITS.

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