Total genomic DNA was extracted from fresh young leaves using a modified CTAB method following procedures described previously (Kovarik et al., 1997). Genomic DNA was digested with the BamHI restriction enzyme and hybridized on blots. The DNAs were digested with BamHI and hybridized with the radioactively labeled ([32P] dCTP, Dekaprimer labeling kit (Thermo Fischer, USA) 5S rDNA probe. The probe was a trimer of the 5S rRNA gene from Artemisia tridentata [S4 clone, GenBank # , ( JX101915.1Garcia et al., 2012b)]. Hybridization signals were visualized using a PhosphorImager (Fuji, FLA 9000).
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