Abstract
The sequences of 18S and 28S rDNAs have been used as molecular markers to resolve phylogenetic relationships of Heteroptera for two decades. The complete sequences of 18S rDNAs have been used in many studies, while in most studies only partial sequences of 28S rDNAs have been used due to technical difficulties of amplifying the complete lengths. In this study, we amplified the complete 18S and 28S rDNA sequences of Eurydema maracandica Oshanin, 1871, and reconstructed the secondary structure models of the corresponding rRNAs. In addition, and more importantly, all of the length variable regions of 18S rRNA were compared among 37 families of Heteroptera based on 140 sequences, and the D3 region of 28S rRNA was compared among 51 families based on 84 sequences. It was found that 8 length variable regions could potentially serve as molecular synapomorphies for some monophyletic groups. Therefore discoveries of more molecular synapomorphies for specific clades can be anticipated from amplification of complete 18S and 28S rDNAs of more representatives of Heteroptera.
Highlights
Each cluster of rDNA in turn contains external transcribed spacer (ETS), 18S rDNA, internal transcribed spacer 1 (ITS1), 5.8S rDNA, ITS2 and 28S rDNA (Hillis, Dixon 1991)
Reconstruction of the complete secondary structure model of 28S rRNA can only be achieved by full sequencing of 28S rDNA
The secondary structure models of 18S and 28S rRNAs of Heteroptera were reconstructed based on corresponding rDNA sequences of the pentatomid species Eurydema maracandica Oshanin, 1871
Summary
Each cluster of rDNA in turn contains external transcribed spacer (ETS), 18S rDNA, internal transcribed spacer 1 (ITS1), 5.8S rDNA, ITS2 and 28S rDNA (Hillis, Dixon 1991). So far only partial sequences of 28S rDNAs have been involved in phylogenetic studies on Heteroptera due to technical difficulties of amplifying the complete lengths. Reconstruction of the complete secondary structure model of 28S rRNA can only be achieved by full sequencing of 28S rDNA.
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