Eucalypt chloroplast DNA (cpDNA) provides useful markers for phylogenetic a
nd population research including gene now and maternity studies. All cpDNA
studies in Eucalyptus to date have been based on the RFLP technique, which
requires relatively large amounts of clean DNA. The objective of this study
was to develop PCR-based cpDNA markers for Eucalyptus. The chloroplast gen
ome of Eucalyptus, like that of most angiosperms, possesses inverted repeat
s (IR). The two junctions between the IRs and the large single copy (LSC) r
egions are defined as J(LA) and J(LB). The region surrounding the J(LA) jun
ction was sequenced from 26 Eucalyptus DNA samples (21 of E: globulus, plus
5 other species), and the J(LB) region was sequenced using 5 of these samp
les. The samples were chosen to represent all major haplotypes identified i
n previous cpDNA RFLP studies. The J(LA) products were 150-210 bp in size,
while those from J(LB) were approximately 500 bp in size. Eighteen mutation
s were scored in total. Extensive variation was found in the IR within the
intergenic spacer between rpl2 and the IR/LSC junctions. Many of these char
acters were complex indels. One sample of E. globulus possessed a relativel
y large (38 bp) insertion which caused displacement of the IR/LSC junctions
. This is the first report of intraspecific variation in the position of IR
/LSC junctions; interspecific variation was also found. The LSC region near
J(LB) had a low rate of mutation and none were informative. The LSC region
near J(LA) possessed 2 informative mutations. The variation revealed from
these sequences reflects the differentiation previously uncovered in an ext
ensive RLFP analysis on the same samples. These results suggest that the J(
LA) region will provide very useful cpDNA polymorphisms for future studies:
in Eucalyptus.