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Comparative Study
doi: 10.1261/rna.7204505.

A common core of secondary structure of the internal transcribed spacer 2 (ITS2) throughout the Eukaryota

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Comparative Study

A common core of secondary structure of the internal transcribed spacer 2 (ITS2) throughout the Eukaryota

Jörg Schultz et al. RNA. 2005 Apr.

Abstract

The ongoing characterization of novel species creates the need for a molecular marker which can be used for species- and, simultaneously, for mega-systematics. Recently, the use of the internal transcribed spacer 2 (ITS2) sequence was suggested, as it shows a high divergence in sequence with an assumed conservation in structure. This hypothesis was mainly based on small-scale analyses, comparing a limited number of sequences. Here, we report a large-scale analysis of more than 54,000 currently known ITS2 sequences with the goal to evaluate the hypothesis of a conserved structural core and to assess its use for automated large-scale phylogenetics. Structure prediction revealed that the previously described core structure can be found for more than 5000 sequences in a wide variety of taxa within the eukaryotes, indicating that the core secondary structure is indeed conserved. This conserved structure allowed an automated alignment of extremely divergent sequences as exemplified for the ITS2 sequences of a ctenophorean eumetazoon and a volvocalean green alga. All classified sequences, together with their structures can be accessed at http://www.biozentrum.uni-wuerzburg.de/bioinformatik/projects/ITS2.html. Furthermore, we found that, although sample sequences are known for most major taxa, there exists a profound divergence in coverage, which might become a hindrance for general usage. In summary, our analysis strengthens the potential of ITS2 as a general phylogenetic marker and provides a data source for further ITS2-based analyses.

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Figures

FIGURE 1.
FIGURE 1.
(A) All-in-one graphical visualization (2D-plot) of the aligned secondary structures from the ITS2 sequences of Beroe ovata (GenBank Identifier gi:14517697) and Pandorina morum (gi:6066293). Compensatory base changes are indicated in red; species-specific sites are in blue (Beroe ovata) and green (Pandorina morum). Black indicates identical nucleotides. Positions within the structures are numbered every 20 nucleotides. Helices are numbered I–IV. (B) An automatically generated global pairwise sequence alignment based on a "universally" conserved secondary structure of both sequences as obtained from RNAforester. In case of Beroe ovata a Y and a W had to be deleted before submission to RNAforester. Note the U-U mismatches as well as the UGGU respectively the UGGGU motifs highlighted in red.

References

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