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Nuclear and mitochondrial DNA polymorphism and phylogeny in the California closed-cone pinesWu, Junyuan 26 August 1998 (has links)
We studied genetic polymorphism and phylogeny using nuclear random amplified
polymorphic DNA markers (RAPDs) and mitochondrial DNA (mtDNA) restriction
fragment length polymorphisms (RFLPs) in the three California Closed-Cone Pines:
Pinus attenuata Lemm., P. muricata D. Don, and P. radiata D. Don. A total of 343 to
384 trees derived from 13 populations were analyzed using 13 mitochondria' gene probes
and two restriction enzymes, and more than 90 RAPD loci generated by 22 primers.
Southern hybridization was used to test homology among comigrating RAPD markers.
Segregation analysis and Southern hybridization were carried out to distinguish between
RAPD fragments of nuclear and organellar origin. Estimates of genetic diversity and
population differentiation, and phylogenetic analyses based on RAPD and RFLP markers,
were compared with those based on allozymes from a similar study.
Twenty-eight distinct mtDNA haplotypes were detected among the three species. All
three species showed limited variability within populations, but strong differentiation
among populations. Based on haplotype frequencies, genetic diversity within populations
(Hs) averaged 0.22, and population differentiation (GsT and 0) exceeded 0.78. Analysis of
molecular variance (AMOVA) also revealed that more than 90% of the variation resided
among populations. Species and populations could be readily distinguished by unique
haplotypes, often using the combination of only a few probes.
Twenty-eight of 30 (93%) comigrating RAPD fragments tested were homologous by
Southern hybridization. Hybridization with enriched mtDNA, and chloroplast DNA
(cpDNA) clones, identified one fragment as being of mtDNA origin and two as being of
cpDNA origin, among 142 RAPD fragments surveyed. RAPD markers revealed moderately higher intrapopulation gene diversity and significantly higher total genetic
diversity and population differentiation than did allozyme markers for each species.
Simulation analysis to study effects of dominance on RAPD diversity suggested that
dominance substantially depressed values of diversity within populations and inflated
values of differentiation among populations. By comparison to our empirical analyses, we
inferred that the underlying diversity of RAPD markers is substantially greater than that
of allozymes.
Results of phylogenetic analysis of RAPD markers were largely consistent with those
from allozyme analysis, though they had many minor differences. Joint phylogenetic
analysis of both the RAPD and allozyme markers strongly supported a common ancestor
for P. radiata and P. attenuata, and south to north migration histories for all three
species. Dendrograms based on mtDNA analysis, however, strongly disagreed with those
based on allozymes, RAPDs, chloroplast DNA and morphological traits, suggesting
convergent genome evolution. / Graduation date: 1999
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Phylogenetics and genomic patterns of speciation in Pinus with an empahsis on subgenus StrobusSyring, John V. 05 May 2006 (has links)
Data from nuclear ribosomal internal transcribed spacer regions (nrITS) and chloroplast DNA
(cpDNA) have failed to resolve phylogenetic relationships in Pinus. To provide greater
interspecific resolution, five low-copy nuclear genes were developed from mapped conifer anchor
loci. Four genes were sequenced from species representing all Pinus subsections. Individual loci
do not uniformly support the nrITS or cpDNA hypotheses. Combined analysis of low-copy
nuclear loci produces a well-supported subsectional topology. The phylogenetic positions of P.
nelsonii and P. krempfii are of systematic interest. Results strongly support P. nelsonii as sister to
sect. Parrya, and suggest a moderately well-supported position of P. krempfii as sister to the
remaining sect. Quinquefoliae. The most informative locus, a Late Embryogenesis Abundant-like
gene, was used to explore phylogenetic relationships among closely related species in subg.
Strobus. Thirty-nine species were sequenced, with two or more alleles representing 33 species.
Nineteen of 33 species exhibited allelic nonmonophyly in the strict consensus tree. Nucleotide
diversity was strongly associated (P<0.0001) with the degree of species monophyly. While
species nonmonophyly complicates phylogenetic interpretations, this locus offers greater
topological support than cpDNA or nrITS. Lacking evidence for hybridization, recombination, or
imperfect taxonomy, incomplete lineage sorting remains the best explanation for trans-species
polymorphisms. The absence of allelic coalescence is a severe constraint in the application of
phylogenetic methods in Pinus, and taxa sharing similar life history traits may show analogous
patterns. While lack of coalescence may limit their utility in traditional phylogenetics, nuclear
genes remain highly informative in describing speciation events. Pinus chiapensis is a threatened
species originally described as a variety of P. strobus. Prior morphological work suggests P.
chiapensis is a distinct species, but that taxonomy is not universally accepted. Multiple accessions
of three probable progenitors were sequenced at three nuclear loci. No interspecific allele sharing
occurs with P. chiapensis, and its alleles are monophyletic at two loci. Results demonstrate that
P. chiapensis is a distinct species. However, determination of the sister species is complicated by
lack of species monophyly and interlocus variability. Pinus ayacahuite is the least likely
progenitor, but the relationship of P. chiapensis to P. monticola or P. strobus is unclear. / Graduation date: 2006
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