Sequence analysis of the hypervariable internal transcribed spacer (ITS) re
gions of ribosomal DNA (rDNA) is commonly used to gain insights into plant
and animal population structure and phylogeny. We characterized ITS1, ITS2,
and the 5.8S coding region of 18 senita (Lophocereus) individuals from 12
different populations in Baja as well as from closely related cactus specie
s. Analyses of multiple clones demonstrated extensive paralogy in the senit
a rDNA gene family. We identified at least two putatively non-recombining r
DNA operons in senita as well as multiple paralogous sequences within each
operon. Usage of PCR, reverse transcriptase (RT)-PCR, Southern blot, primar
y sequence analyses of the 18S rDNA gene, and secondary structure analyses
of the 5.8S rRNA showed that one of the operons encodes rDNA pseudogenes in
a low copy-number (Truncated), whereas the second operon encodes an expres
sed rRNA (Functional). Surprisingly, we found extensive paralogy not only i
n the ITS regions but also in the 5.8S coding regions in senita both within
and between operons. Phylogenetic analyses suggest that the second rDNA op
eron originated prior to the divergence of Lophocereus. A significant (p <
0.05) divergence-rate acceleration was found in the Lophocereus 5.8S rDNA c
oding region in the Functional operon in comparison to Pereskiopsis porteri
(Cactaceae) and Portulaca molokiniensis (Portulacaceae) with Silent dioica
and Spinacia oleracea as the outgroups.