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- Author or Editor: Hongwen Huang x
Thirty-four extant pawpaw [Asimina triloba (L.) Dunal] cultivars and advanced selections representing a large portion of the gene pool of cultivated pawpaws were investigated using 71 randomly amplified polymorphic DNA (RAPD) markers to establish genetic identities and evaluate genetic relatedness. All 34 cultivated pawpaws were uniquely identified by as few as 14 loci of eight primers. Genetic diversity of the existing gene pool of cultivated pawpaws, as estimated by Nei's gene diversity (He), was similar to that of wild pawpaw populations. The genetic relatedness among the cultivated pawpaws examined by UPGMA cluster analysis separated 34 cultivars and selections into two distinct clusters, a cluster of PPF (The PawPaw Foundation) selections and a cluster including a majority of the extant cultivars selected from the wild and their derived selections. The results are in general agreement with the known selection history and pedigree information available. The consensus fingerprint profile using the genetically defined RAPD markers is a useful and reliable method for establishing the genetic identities of the pawpaw cultivars and advanced selections. This also proved to be an improved discriminating tool over isozyme markers for the assessment of genetic diversity and relatedness. RAPD profiling of data presented in this study provides a useful reference for germplasm curators engaged in making decisions of sampling strategies, germplasm management and for breeders deciding which parents to select for future breeding efforts.
The utility of isozyme phenotypes for identifying and determining genetic variation in pawpaw cultivars was studied using isoelectric focusing in thin-layer polyacrylamide gels. Based on a sample of 32 clones (cultivars and advanced selections) and 23 enzyme systems, 7 enzymes were found to be polymorphic, involving 9 polymorphic loci [acid phosphatase (ACP), dihydrolipoamide dehydrogenase (DDH), malic enzyme (ME), phosphoglucoisomerase (PGI), phosphoglucomutase (PGM), peroxidase (PRX), and shikimate dehydrogenase (SKD)]. Altogether these 9 loci and 32 clones yielded 28 multi-locus isozymic phenotypes useful for cultivar identification; 24 of the 32 clones were uniquely identified. The allozyme variation in these clones has the average of other long-lived woody perennials of widespread geographic range in temperate regions with insect-pollinated outcrossing breeding systems, secondary asexual reproduction, and animal-dispersed seed. Genetic differentiation among these pawpaw clones, measured by Nei's distance, D, was substantial: 496 pairwise comparisons of genetic distance among the 32 clones indicated that they differed on average of D = 0.068 ± 0.04 and ranged from 0 to 0.188. Cluster analysis (UPGMA) produced a most likely division of the 32 clones into 7 groups; however, these groups did not conform to known pedigree relations. Additional polymorphic enzymes are needed for accurate allozyme-based genetic discrimination.
As a new National Clonal Germplasm Repository for Asimina species at Kentucky State University (KSU), of major concern to us is the genetic variation within our germplasm collection. The present study investigated the extent of genetic diversity for the pawpaw germplasm in our collection and the geographical pattern of genetic diversity among populations using isozyme markers. Allozyme diversity was high in Asimina triloba (L.) Dunal (Annonaceae) collected from all nine different states, as is typical for temperate woody perennial, widespread and outcrossing plant species. Averaged across populations, mean number of alleles per locus (A), percent polymorphic loci (P), effective number of alleles per locus (Ae), and expected heterozygosity (He) were 1.54, 43.5, 1.209, and 0.172, respectively. Significant deviations from Hardy-Weinberg equilibrium were found in nine populations at an average of 4.8 loci. Observed heterozygosity was higher than expected. Partitioning of genetic diversity showed that 88.2% resided within populations. The proportion of genetic diversity among populations (Gst = 0.118; FST = 0.085) was either lower than or within the range of those species with similar ecological and life-history traits. The mean genetic identity among populations was high (I = 0.988). An analysis using UPGMA clustered most populations as one major group, with the southernmost (Georgia) and the westernmost (Illinois) populations readily separated from the main group. The relationships discovered by principal component analysis (PCA) were similar to those revealed by UPGMA. In addition, PCA separated the northernmost population (New York) from the major group. Sampling strategies for future germplasm collection of A. triloba are also discussed.
Twelve, 10-base primers amplified a total of 20 intense and easily scorable polymorphic bands in an interspecific cross of PPF1-5 pawpaw [Asimina triloba (L.) Dunal.] × RET (Asimina reticulata Shuttlew.). In this cross, all bands scored were present in, and inherited from, the A. triloba parent PPF1-5. Nineteen of the 20 bands were found to segregate as expected (1:1 or 3:1) based on chi-square goodness-of-fit tests, and were subsequently used to evaluate genetic diversity in populations of A. triloba collected from six states (Georgia, Illinois, Indiana, Maryland, New York, and West Virginia) within its natural range. Analysis of genetic diversity of the populations revealed that the mean number of alleles per locus was A = 1.64, percent polymorphic loci was P = 64, and expected heterozygosity was He = 0.25. No significant differences were found among populations for any of the polymorphic indices. Partitioning of the population genetic diversity showed that the average genetic diversity within populations was Hs = 0.26, accounting for 72% of the total genetic diversity. Genetic diversity among populations was Dst = 0.10, accounting for 28% of the total genetic diversity. Nei's genetic identity and distance showed a high mean identity of 0.86 between populations. Genetic relationships among the populations examined by unweighted pair-group mean clustering analysis separated the six populations into two primary clusters: one composed of Georgia, Maryland, and New York, and the other composed of Illinois, Indiana, and West Virginia. The Georgia and Indiana populations were further separated from the other populations within each group. This study provides additional evidence that marginal populations within the natural range of A. triloba should be included in future collection efforts to capture most of the rare and local alleles responsible for this differentiation.
The genus Castanea (Fagaceae), which contains three sections and seven species, is widely distributed in the deciduous forests of the Northern Hemisphere. The phylogeny of Castanea was estimated using DNA sequence data from five different regions of the chloroplast genome. Sequencing results support the genus Castanea as a paraphyletic group with C. crenata, the Japanese chestnut, representing an early divergence in the genus. The three Chinese species form a strongly supported sister clade to the North American and European clade. A unique westward expansion of extant Castanea species is hypothesized with Castanea originating in eastern Asia, an initial diversification within Asia during the Eocene, followed by intercontinental dispersion and divergence between the Chinese and European/North American species during the Oligocene and a split between the European and North American species in the early Miocene. The differentiation within North America and China might have occurred in late Miocene or early Pliocence. The North America species are supported as a clade with C. pumila var. ozarkensis, the Ozark chinkapin, as the basal lineage, sister to the group comprising C. pumila var. pumila, the Allegheny chinkapin, and C. dentata, the American chestnut. Morphological evolution of one nut per bur in the genus may have occurred independently on two continents.
The sand pear (Pyrus pyrifolia Nakai) is an important fruit crop in China. In this study, simple sequence repeats (SSRs) were used to estimate the level and pattern of genetic diversity among 233 sand pear landraces collected from 10 different geographic regions in China. The results demonstrated that the SSR technique is an effective tool for assessing genetic diversity and the geographic pattern of genetic variation among sand pear landraces of different origins. A total of 184 putative alleles was detected using 14 primer pairs with an average of 13.1 alleles per locus. The mean expected heterozygosity and observed heterozygosity across all loci were 0.705 and 0.671, respectively. High genetic diversity was found in all populations except for that originated from Jiangxi (A e = 3.149; H e = 0.655), whereas at the regional level, those from central China were less diverse than those from other regions. Analysis of molecular variance showed that most genetic differences resided among landraces within populations. Additionally, unweighted pair group with arithmetic average clustering and principal component analysis plotting based on Nei's genetic distance revealed distinct gene pools in agreement with geographic distribution.
Isozyme inheritance and variation in Actinidia was investigated using 23 enzyme systems. Ten isozyme loci from six enzyme systems, Acp-2, Est, Prx-1, Prx-2, Prx-4, Prx-5, Pgi-2, Pgm-2, and Tpi, were found to be inherited as single Mendelian genes in families of two interspecific crosses. Disomic inheritance detected at ten loci in progenies of a cross between the hexaploid A. deliciosa × diploid A. chinensis, provided convincing evidence that A. deliciosa is an allohexaploid. Allelic segregation for tetrasomic inheritance at ten isozyme loci was demonstrated in the progenies of a cross between the tetraploid A. chinesis × diploid A. eriantha, a result suggesting the autotetraploid origin of the tetraploid A. chinensis which apparently originated from its diploid ancestor A. chinensis. A high level of isozyme variation and heterozygosity were observed in the 22 cultivars and 56 plants of 28 Actinidia taxa. Allozyme phenotype can be used effectively for cultivar identification.
On March 13-15, 1993 Alabama and much of the eastern United States experienced an unusually severe winter storm. This afforded the evaluation of plum cultivar production under cold stress. The highest yielding variety that bloomed before the storm was Bruce 12-4 with 28 kg/tree. Bruce 12-4 is noted for blooming over an extended period of time and producing very heavy yields. The average yield of the top five performers that bloomed after the storm was 51 kg/tree. The lowest temperature recorded at the test site, Shorter, AL was -5C.
Forty eight cultivars, species, and their progeny including Prunus americana P. angustifolia, P. cerasifera P. munsoniona, P. salicina, P. simoni, and P. triflora were evaluated for resistance to Xylella fastidiosa based on percent of scalded leaves and tree longevity. Observations indicate that resistance is heritable and controlled by recessive genes. Further, X. fastidiosa transmission was evaluated in plum and peach by chip and slip budding. Transmission as measured by enzyme-linked immunoabsorbant assay indicated that chip budding resulted in a higher level of transmission over slip budding in plum but not in peach. Neither Lovell nor Nemaguard rootstock had an effect on transmission.