Abstract

The internal transcribed spacer (ITS) of ribosomal DNA has been used to confirm taxonomic classifications and define phylogenies in several plant species following sequencing or polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) techniques. In this study, co-dominant ITS PCR-RFLP molecular markers were produced in 30 Fagaceae individuals belonging to the Castanea, Fagus and Quercus genera in order to assess the potential of this technique for taxonomic discrimination and determination of phylogenies. The complete ITS region (ITS1-5.8S rRNA-ITS2) was amplified in most of the Fagaceae individuals as a single fragment of ∼700 bp. The ITS amplified products were digested with nine restriction enzymes, but only four (HaeIII, HpaII, TaqI and Sau96I) produced polymorphic/discriminative patterns. The total expected heterozygosity (HE) was 20.31 % and the gene diversity (I), 32.97 %. The ITS polymorphism was higher within the Quercus genus (85.3 %). The ITS PCR-RFLP markers clustered the Fagaceae species according to genus or infrageneric group (in the case of Quercus sp. individuals). Five oaks did not cluster in line with the adopted infrageneric classification, but three of these were grouped according to their actual ecological distributions. The ITS PCR-RFLP markers indicated their potential for phylogenetic studies since all Fagaceae individuals were discriminated according to genus, and most of the oaks were clustered according to infrageneric group or ecological area.

Highlights

  • Ribosomal DNA is a nuclear multigene family with copies arranged in tandem arrays within the nucleolar organizer regions (NORs) that form the secondary chromosomal constriction, with the centromere being the primary constriction (McClintock 1934; Navashin1934)

  • We aimed to investigate the potential of the internal transcribed spacer (ITS) PCR – restriction fragment length polymorphism (RFLP) markers for taxonomic discrimination and determination of phylogenies, with a particular focus on the genus Quercus

  • Phylogenetic studies based on ITS sequencing often detect, beyond point mutations, short nucleotide insertions/deletions responsible for the variable length of the ITS1-5.8S-ITS2 region

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Summary

Introduction

Ribosomal DNA (rDNA) is a nuclear multigene family with copies arranged in tandem arrays within the nucleolar organizer regions (NORs) that form the secondary chromosomal constriction, with the centromere being the primary constriction (McClintock 1934; Navashin1934). Each rDNA unit is composed of the conserved coding regions of the 18S-5.8S-26S rRNA genes, including the variable non-coding intergenic spacer (IGS). The IGS itself consists of a non-transcribed spacer region containing motifs that are designated as sub-repeats and is flanked by external transcribed spacers. The 5.8S rRNA gene is flanked by two non-coding sequences referred to as the Published by Oxford University Press on behalf of the Annals of Botany Company.

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