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Cellulose microfibrils are the major structural component of plant secondary cell walls. Their arrangement in plant primary cell walls, and its consequent influence on cell expansion and cellular morphology, is directed by cortical microtubules; cylindrical protein filaments composed of heterodimers of alpha- and beta-tubulin. In secondary cell walls of woody plant stems the orientation of cellulose microfibrils influences the strength and flexibility of wood, providing the physical support that has been instrumental in vascular plant colonization of the troposphere. Here we show that a Eucalyptus grandisbeta-tubulin gene (EgrTUB1) is involved in determining the orientation of cellulose microfibrils in plant secondary fibre cell walls. This finding is based on RNA expression studies in mature trees, where we identified and isolated EgrTUB1 as a candidate for association with wood-fibre formation, and on the analysis of somatically derived transgenic wood sectors in Eucalyptus. We show that cellulose microfibril angle (MFA) is correlated with EgrTUB1 expression, and that MFA was significantly altered as a consequence of stable transformation with EgrTUB1. Our findings present an important step towards the production of fibres with altered tensile strength, stiffness and elastic properties, and shed light on one of the molecular mechanisms that has enabled trees to dominate terrestrial ecosystems.

Most conifer species occur in large continuous populations, but radiata pine, Pinus radiata, occurs only in five disjunctive natural populations in California and Mexico. The Mexican island populations were presumably colonized from the mainland millions of years ago. According to Axelrod (1981), the mainland populations are relicts of an earlier much wider distribution, reduced some 8,000 years ago, whereas according to Millar (1997, 2000), the patchy metapopulation-like structure is typical of the long-term population demography of the species. We used 19 highly polymorphic microsatellite loci to describe population structure and to search for signs of the dynamics of population demography over space and time. Frequencies of null alleles at microsatellite loci were estimated using an approach based on the probability of identity by descent. Microsatellite genetic diversities were high in all populations [expected heterozygosity (H(e)) = 0.68-0.77], but the island populations had significantly lower estimates. Variation between loci in genetic differentiation (F(ST)) was high, but no locus deviated statistically significantly from the rest at an experiment wide level of 0.05. Thus, all loci were included in subsequent analysis. The average differentiation was measured as F(ST) = 0.14 (SD 0.012), comparable with earlier allozyme results. The island populations were more diverged from the other populations and from an inferred common ancestral gene pool than the mainland ones. All populations showed a deficiency of expected heterozygosity given the number of alleles, the mainland populations more so than the island ones. The results thus do not support a recent important contraction in the mainland range of radiata pine.

Eucalyptus leucoxylon is a widespread woodland tree species found in southeastern Australia that has suffered from, and continues to be, threatened by the impacts of habitat clearance and degradation. Populations now consist predominantly of scattered individuals, and their conservation status is of increasing concern. We report the development and characterization of a set of eight highly polymorphic microsatellite loci for E. leucoxylon. The loci can be amplified in three PCR multiplexes and electrophoresed in a single lane, allowing rapid throughput of large numbers of samples. A total of 111 alleles were detected in 68 individuals with an average of 12.3 alleles per locus, a mean expected heterozygosity of 0.83, and a mean observed heterozygosity of 0.72. The combined probabilities of identity and probabilities of paternity exclusion allow an extremely precise level of individual identification, indicating that these microsatellite markers will be ideal for population genetic and parentage-type studies in E. leucoxylon. The markers also exhibited an average of 76% conservation within the subgenus Symphyomyrtus, to which E. leucoxylon belongs, and 53% conservation across other subgenera of Eucalyptus, demonstrating the potential of these markers in ecological and breeding studies in a wide range of Eucalyptus species.

Ten microsatellite loci were used to DNA profile 215 first and second generation breeding clones in the Australian radiata pine breeding program. The clones were essentially unique from one another and these DNA profiles were used to examine the sexual and asexual phases in the breeding program. Only 2.6% of ramets from 25 breeding clones were incorrect whereas 8.4% of progeny from 10 families were genetically incorrect. The lineages of second generation clones were checked for DNA profiles that were available for putative parents. Some parents appear to be incorrect on the basis of the DNA profiles and further sampling will be required to confirm these results across the breeding program. Microsatellite markers can now enable most questions to be resolved in breeding programs and also will allow novel breeding strategies to be used in the future.

Pinus radiata has a history of population bottlenecks and is currently restricted to five relatively small populations, three in mainland California, and two on islands off the coast of Baja California. Using highly polymorphic microsatellite markers and a newly developed statistical approach, we were able to estimate individual inbreeding coefficients and can thus analyse the mating system with high resolution. We find a bimodal distribution of inbreeding coefficients: most individuals result from selfing whereas few (in the mainland populations) to a modest number (in the island populations) are likely selfed. In most other pine species and presumably in the ancestral P. radiata population, occurrence of mature selfed individuals would be impossible because of the high genetic load. We therefore conclude that inbreeding depression has been purged in P. radiata and that the mating system has changed as a consequence.

Eight dinucleotide microsatellites were developed in Eucalyptus sieberi L. Johnson (silvertop ash), a member of the subgenus Eucalyptus. Transfer of six of these to the subgenus Symphyomyrtus and their Mendelian inheritance are demonstrated using a full-sib cross in Eucalyptus nitens. Genetic diversity parameters are presented for the eight loci based on a sample of 100 old-growth E. sieberi trees from a single natural stand. One locus, Es266, had an atypically high fixation index, and significantly deviated from Hardy-Weinberg equilibrium genotypic proportions, indicating the likely presence of null alleles. Two of the loci, Es076 and Es140, had many alleles that differed in size by only a single base pair, possibly because of short poly(A) or poly(T) stretches in their flanking regions. These two loci were by far the most polymorphic, but were difficult to score reliably on a capillary DNA sequencer. Reliability of scoring of these two one-base microsatellite loci was markedly improved by the incorporation of internal reference alleles into each sample analysed.Key words: SSRs, single base pair alleles, null alleles, internal reference alleles.

Genetic diversity in the nuclear genome of Eucalyptus nitens was assessed using 40 anonymous RFLP loci. Information about the RFLP probes was available from the genetic linkage map of the species and probes that detected single loci were selected to cover the whole of the genome. Several loci that were monomorphic in the mapping pedigree were also used to avoid bias towards polymorphic loci. Variation was determined for 20 individuals from each of eight populations covering the natural range of the species. The proportion of rare alleles detected in populations ranged from 21% to 49%. The level of diversity within the nuclear genome was high (AS = 6.9, PS = 92.5%, HT = 0.445) compared with other species where RFLP surveys have been conducted. The level of variation detected was higher for RFLP loci than for isozyme loci, but the patterns of genetic diversity were similar for both marker types. Population similarities based on RFLP analysis of the nuclear genome were not concordant with those based on the chloroplast genome.

Genetic diversity in the nuclear genome of Acacia mangium was estimated using 57 anonymous RFLP loci for 10 individuals from each of 10 natural populations representing the geographical range of the species. The level of genetic diversity varied significantly among the populations, ranging from HE=0.01 on the island of Ceram to HE=0.21 in Muting, New Guinea. The small, geographically isolated populations of Daintree, Townsville, Ceram and Sidei had low levels of diversity (HE=0.01–0.09) whereas the large New Guinea and the Cape York Peninsula populations had higher levels of diversity (HE=0.16–0.21). There was evidence of genetic differentiation between populations (θ=0.35), 75% of which was attributable to differences between four geographical regions of Cape York and Daintree–Townsville in Australia, New Guinea and Ceram–Sidei. This may reflect restrictions to gene flow associated with past expansions and contractions of rainforests which occurred with climate and sea level changes. The level of variation detected with RFLPs was higher than previously detected with allozymes, supporting speculation that allozyme coding regions are more likely to be constrained by selection than noncoding regions. The distribution of variation within and among populations was consistent for the two marker types.

Melaleuca alternifolia andM. linariifolia are commercially important Australian species harvested for their essential oils. Both species have relatively narrow and disjunct distributions on the central coast of eastern Australia. Variation in the chloroplast genome was assessed for eight individuals from each of twelve populations, representing the species' geographic range. Low nucleotide diversity withinM. alternifolia contrasted with high nucleotide diversity inM. linariifolia. CpDNA data are consistent with the southern population ofM. alternifolia being a hybrid population withM. linariifolia. The two species are sympatric in this region. Variation inM. linariifolia was geographically structured, with northern populations differing from southern populations by seven restriction site mutations, five length mutations and an inversion. There was no evidence of hybridisation of the cp genome of northernM. linariifolia with the partially sympatric speciesM. trichostachya. Intra- and interspecific variation in the chloroplast genomes ofM. alternifolia, M. linariifolia, andM. trichostachya indicate considerable potential for the use of intraspecific cpDNA studies in examining phylogenetic relationships in melaleucas.

Variation in the chloroplast genome of Eucalyptus nitens was assessed for ten individuals from each of eight populations covering the natural range of the species. Twenty-five mutations were detected which were distributed over 13 haplotypes. The mutations were present both within and between populations. The level of nucleotide diversity within the species was high and the majority of the variation was distributed between populations and regions. The level and distribution of haplotype diversity were similar to those of the nucleotide diversity. The interpopulational variation may be related to the large range and disjunct populations that characterize the species, due to the effects of isolation and genetic drift. There were three mutations which were unique and fixed in one small population. Individuals in the species could be distinguished into two cpDNA groups. The distribution of these groups was not consistent with any geographical pattern. The distribution of the cpDNA groups suggests that they are of ancient origin and predate the isolation of the regions. The pattern of cpDNA variation is not consistent with patterns of variation in morphological traits.

Background Eucalyptus trees (family Myrtaceae) are well-known for their high foliar content of several classes of secondary metabolites and these have a strong effect on the feeding patterns of several species of marsupials and at least some insects. Best known are the essential oils, which is mostly a mixture of terpenoids, but there are also significant concentrations of flavonoid and formylated phloroglucinol compounds. There is extensive quantitative and qualitative variation within and between species of Myrtaceae in these chemical groups and all appear to be under strong genetic control with heritabilities (H 2 ) between 0.3 and 0.9. As well as being important ecologically, the terpenes in particular are valued as industrial and medicinal products and Australia supports a strong essential oil industry focused on Eucalyptus and Melaleuca foliar oils. Results and discussion The Eucalyptus grandis genome provides the opportunity to discover the genetic makeup of the biosynthetic pathways for secondary metabolites. We present data from pathways leading into the biosynthesis of terpenes, flavonoids and lignins. The homology of genes and gene families were investigated and compared to a variety of other species including poplar (Populus trichocarpa), grape (Vitis vinifera) and apple (Malus x domesticus). For example, terpene synthases (the gene family responsible for the final step in the terpene biosynthesis) has 120 members in the genome of Eucalyptus grandis, compared to 44 and 99 in poplar and grape, respectively (Table 1). Genes of the biosynthetic pathways for secondary metabolites were mapped to the Eucalyptus grandis genome and their location was compared to a number of quantitative trait loci (QTL) studies that investigated variability in secondary metabolites and wood properties in eucalypts. This approach allowed the discovery of candidate genes for a large number of QTL. Understanding the genetic basis of variations in quantitative traits provides insights into ecosystem function and at the same time may help breeders in the essential oil industry. We have characterized trait associations with polymorphisms from Eucalyptus globulus ,i nvestigating 200 SNPs and roughly 40 traits ranging from terpenoids to terpene-adducts to flavonoids and to tanninrelated traits. We discovered several significant trait associations between allelic variants in the chloroplastic MEP pathway and monoterpenes and between the cytosolic MVA pathway and sesquiterpenes, as well as one allelic variant in a prenyl pyrophosphate synthase that associates with the ratio of monoterpenes to sesquiterpenes. Loci with significant associations were mapped to the Eucalyptus grandis genome and compared to published QTL datasets that investigated similar traits. These results represent the first species wide analysis of

Eucalyptus is characterized by high foliar concentrations of plant secondary metabolites with marked qualitative and quantitative variation within a single species. Secondary metabolites in eucalypts are important mediators of a diverse community of herbivores. We used a candidate gene approach to investigate genetic associations between 195 single nucleotide polymorphisms (SNPs) from 24 candidate genes and 33 traits related to secondary metabolites in the Tasmanian Blue Gum (Eucalyptus globulus). We discovered 37 significant associations (false discovery rate (FDR) Q < 0.05) across 11 candidate genes and 19 traits. The effects of SNPs on phenotypic variation were within the expected range (0.018 < r(2) < 0.061) for forest trees. Whereas most marker effects were nonadditive, two alleles from two consecutive genes in the methylerythritol phosphate pathway (MEP) showed additive effects. This study successfully links allelic variants to ecologically important phenotypes which can have a large impact on the entire community. It is one of very few studies to identify the genetic variants of a foundation tree that influences ecosystem function.

The 5S RNA genes inPinus radiata occur in two size classes of about 850 and 525 bp in length. Representatives from both the long and short size classes were cloned and sequenced. The primary difference in the two size classes was shown to be a 330 bp insertion in the spacer region of the long units. Within an individual breeding clone ofP. radiata there was some sequence heterogeneity between representatives of the short class. The 5S RNA genes in thirty pine species were characterised using either a clone of the short size class or a subclone of the 330 bp insertion characterizing the long size class. Eleven species of subg.Strobus were examined and all lacked the long type of unit of radiata pine. The New World species of subg.Pinus all had both short and long units whereas the Old World species had long units. The implications of these results for the evolution of the 5S DNA sequences and the phylogenetic relationships withinPinus are discussed.

Background There is little information about the DNA sequence variation within and between closely related plant species. The combination of re-sequencing technologies, large-scale DNA pools and availability of reference gene sequences allowed the extensive characterisation of single nucleotide polymorphisms (SNPs) in genes of four biosynthetic pathways leading to the formation of ecologically relevant secondary metabolites in Eucalyptus. With this approach the occurrence and patterns of SNP variation for a set of genes can be compared across different species from the same genus. Results In a single GS-FLX run, we sequenced over 103 Mbp and assembled them to approximately 50 kbp of reference sequences. An average sequencing depth of 315 reads per nucleotide site was achieved for all four eucalypt species, Eucalyptus globulus, E. nitens, E. camaldulensis and E. loxophleba. We sequenced 23 genes from 1,764 individuals and discovered 8,631 SNPs across the species, with about 1.5 times as many SNPs per kbp in the introns compared to exons. The exons of the two closely related species (E. globulus and E. nitens) had similar numbers of SNPs at synonymous and non-synonymous sites. These species also had similar levels of SNP diversity, whereas E. camaldulensis and E. loxophleba had much higher SNP diversity. Neither the pathway nor the position in the pathway influenced gene diversity. The four species share between 20 and 43% of the SNPs in these genes. Conclusion By using conservative statistical detection methods, we were confident about the validity of each SNP. With numerous individuals sampled over the geographical range of each species, we discovered one SNP in every 33 bp for E. nitens and one in every 31 bp in E. globulus. In contrast, the more distantly related species contained more SNPs: one in every 16 bp for E. camaldulensis and one in 17 bp for E. loxophleba, which is, to the best of our knowledge, the highest frequency of SNPs described in woody plant species.

Paternity analysis can be used to estimate mean effective pollen dispersal (micro(d)) by sampling offspring from a mother plant and assaying each for a large number of allozyme loci. The male in the population with the highest likelihood of paternity, based entirely on the degree of genetic relationship with the offspring (transition probability) or combined with information on probability of mating with the mother plant, is inferred as the pollen parent. Computer simulations show that the mean distance between inferred males and mother plants (d) reliably estimates micro(d) in defined circumstances. If male mating success decreases with distance from the mother plant, paternity inference based entirely on transition probabilities results in d values that are upwardly biased, perhaps considerably. More reliable estimates can be obtained in this situation when prior information on the general form of the relationship between mating success and distance between mates (the distance function) is used, along with transition probabilities, to infer paternity. However, this procedure is valid only when the general form of the distance function can be reliably assumed. Computer simulations also show that the bootstrap method can be used to closely approximate the SE of .

Pollen of acacias is transported by insects as polyads, composite pollen grains. The polyad has enough pollen grains to fertilize all ovules within a flower and hence all seed within a pod may be full sibs. Isozyme markers were used to test this hypothesis in two populations of Acacia melanoxylon R.Br. The proportions of fruit pods with multiple paternity detected in two populations were 0.08 and 0.15. The proportions of fullsib pairs within pods estimated by the sibling pair method were 1 and 0.63 for the two populations. Comparison of the diploid paternal genotypes of pods of single paternity showed that the probability of a common pollen source for a pair of pods was high within globular clusters (0.35) or within inflorescences (0.46) but declined to 0.10 or 0.25 within the tree at random. Thus the reproductive system acted to reinforce a hierarchy of paternal correlation within each tree.

In response to gravitational stresses, angiosperm trees form tension wood in the upper sides of branches and leaning stems in which cellulose content is higher, microfibrils are typically aligned closely with the fibre axis and the fibres often have a thick inner gelatinous cell wall layer (G-layer). Gene expression was studied in Eucalyptus nitens branches oriented at 45 degrees using microarrays containing 4900 xylem cDNAs, and wood fibre characteristics revealed by X-ray diffraction, chemical and histochemical methods. Xylem fibres in tension wood (upper branch) had a low microfibril angle, contained few fibres with G-layers and had higher cellulose and decreased Klason lignin compared with lower branch wood. Expression of two closely related fasciclin-like arabinogalactan proteins and a beta-tubulin was inversely correlated with microfibril angle in upper and lower xylem from branches. Structural and chemical modifications throughout the secondary cell walls of fibres sufficient to resist tension forces in branches can occur in the absence of G-layer enriched fibres and some important genes involved in responses to gravitational stress in eucalypt xylem are identified.

Summary • Leaves of eucalypt species contain a variety of plant secondary metabolites, including terpenoids and formylated phloroglucinol compounds (FPCs). Both terpene and FPC concentrations are quantitative traits that can show large variation within a population and have been shown to be heritable. The molecular genetic basis of this variation is currently unknown. • Progeny from a field trial of a three-generation mapping pedigree of Eucalyptus nitens were assayed for terpenes and FPCs. Quantitative trait loci (QTL) analyses were conducted using a map constructed from 296 markers to locate regions of the genome influencing foliar concentrations of these plant secondary compounds. • A large number of significant QTL for 14 traits were located across nine linkage groups, with significant clustering of QTL on linkage groups 7, 8 and 9. As expected, QTL for biosynthetically related compounds commonly colocated, but QTL for unrelated monterpenes and FPCs also mapped closely together. • Colocation of these QTL with mapped candidate genes from the various biosynthetic pathways, and subsequent use of these genes in association mapping, will assist in determining the causes of variation in plant secondary metabolites in eucalypts.

Linkage disequilibrium (LD) mapping using natural populations results in higher resolution of marker-trait associations compared to family-based quantitative trait locus (QTL) studies. Depending on the extent of LD, it is possible to identify alleles within candidate genes associated with a trait. Analysis of a natural mutant in Arabidopsis has shown that mutations in cinnamoyl CoA reductase (CCR), a key lignin gene, affect physical properties of the secondary cell wall such as stiffness and strength. Using this gene, we tested whether LD mapping could identify alleles associated with microfibril angle (MFA), a wood quality trait affecting stiffness and strength of wood. We identified 25 common single-nucleotide polymorphism (SNP) markers in the CCR gene in Eucalyptus nitens. Using single-marker and haplotype analyses in 290 trees from a E. nitens natural population, two haplotypes significantly associated with MFA were found. These results were confirmed in two full-sib families of E. nitens and Eucalyptus globulus. In an effort to understand the functional significance of the SNP markers, we sequenced the cDNA clones and identified an alternatively spliced variant from the significant haplotype region. This study demonstrates that LD mapping can be used to identify alleles associated with wood quality traits in natural populations of trees.

Fifty microsatellite markers were developed and characterized in Pinus radiata, and from among these, a subset of 10 easily scored and highly polymorphic markers was selected for use in fingerprinting, quality control, and breeding applications. The markers were characterized based on reliable and reproducible amplification, observed and expected heterozygosities, number of alleles, a low frequency of null alleles, and a lack of close linkage with other selected markers. Allele numbers and frequencies were estimated using 24 first-generation breeding clones from Australia and New Zealand. Observed heterozygosities for the selected markers were all greater than 0.67, and there was an average of 10.5 alleles/locus. The occurrence of null alleles was checked with megagametophytes from mother trees for loci that appeared to be homozygous. The 10 markers are not closely linked (r < 0.20 and LOD > 3) to each other. The selected microsatellites fall into three discrete size classes, and with appropriate selection of fluorescent dyes for 5' end labeling, can be multiplexed with up to 6 markers/sample on an ABI PRISM 310 or similar instrument.Key words: pine microsatellites, multiplexing, null alleles.

Eight dinucleotide microsatellites were developed in Eucalyptus sieberi L. Johnson (silvertop ash), a member of the subgenus Eucalyptus. Transfer of six of these to the subgenus Symphyomyrtus and their Mendelian inheritance are demonstrated using a full-sib cross in Eucalyptus nitens. Genetic diversity parameters are presented for the eight loci based on a sample of 100 old-growth E. sieberi trees from a single natural stand. One locus, Es266, had an atypically high fixation index, and significantly deviated from Hardy-Weinberg equilibrium genotypic proportions, indicating the likely presence of null alleles. Two of the loci, Es076 and Es140, had many alleles that differed in size by only a single base pair, possibly because of short poly(A) or poly(T) stretches in their flanking regions. These two loci were by far the most polymorphic, but were difficult to score reliably on a capillary DNA sequencer. Reliability of scoring of these two one-base microsatellite loci was markedly improved by the incorporation of internal reference alleles into each sample analysed.

International audience; A major focus of our research has been on using molecular technologies to guide breeding for high value wood and fibre traits in eucalypts. One approach has been to use genomic maps to locate and characterise QTL that control wood and fibre traits. A generic map for eucalypts has been developed that consists of codominant markers that can be assayed across the major commercial species. Also on the map are candidate genes for traits such as flowering and wood and fibre traits. QTL have been characterised for wood density, fibre length, pulp yield and microfibril angle. A number of these have been validated in a related pedigree. A subset of QTL colocates with candidate genes. Research is now focussed on DNA sequence variation in different parts of these candidate genes and determining if this variation is associated with variation in wood properties. Of particular interest are genes involved in fibre development and cell wall formation. A third approach is to profile the expression of genes in the tissue of interest and determine if this relates to variation in trait performance. Microarrays are being used to relate expression of several thousand genes in xylem tissue to variation in traits such as microfibril angle and density.; Génomique des critères de qualité du bois d'eucalyptus. Notre recherche a été concentrée sur l'utilisation de technologies moléculaires pour guider l'amélioration génétique de critères importants de la qualité du bois et des fibres. On a développé une carte générique pour les eucalyptus à partir de marqueurs co-dominants intéressant les principales espèces d'intérêt commercial. Figurent également sur cette carte des gènes candidats concernant des caractères tels que la floraison et la qualité du bois et des fibres. On a mis en évidence des QTL pour la densité du bois, la longueur des fibres, le rendement en pâte et l'angle des microfibrilles. Un certain nombre ont été validés sur des familles apparentées à généalogie connue. Un sous ensemble de QTL sont co-localisés avec des gènes candidats. On concentre maintenant les recherches sur la variabilité de séquences ADN de ces gènes candidats pour savoir si elle est associée à celle des critères de qualité du bois. Sont d'un intérêt particulier les gènes impliqués dans le développement des fibres et la formation des parois cellulaires. Une troisième approche consiste à profiler l'expression des gènes dans les tissus en cause et à rechercher s'il existe d'éventuelles relations avec la variabilité des caractères. On utilise des microréseaux pour relier l'expression de plusieurs milliers de gènes du xylème avec la variabilité de caractères tels que l'angle des microfibrilles et la densité du bois.

Eucalyptus camaldulensis Dehnh. is the most widely planted eucalypt in the tropics. Natural populations are riparian and sampling strategies for breeding programmes have assumed that gene flow among drainage basins is limited. RFLP variation, within and among 31 populations from river systems across northern Australia, was analysed to test this hypothesis. To allow comparisons within and between river systems, trees were sampled from up to three populations per river system. Allele frequencies were correlated with longitude for more than half the 33 RFLP loci surveyed. Genetic identity was greatest between populations in closest geographic proximity, irrespective of river system, suggesting that sampling strategies for breeding programmes should be based on geographic distance rather than river system. The level of genetic variation was similar throughout the geographic range examined (mean H(E) = 0.49). However, there was evidence of a barrier to gene flow between populations in the east and west of the species range. The RFLP data support morphological evidence of hybridisation between E. camaldulensis and E. tereticornis Sm. in several populations in northeast Queensland and the genetic divergence of E. camaldulensis subsp. simulata Brooker and Kleinig.

Polymorphisme de 30 loci etudie chez 11 populations d'Acacia mangium du Nord de l'Australie et de la Papouasie et comparaison avec la diversite genetique d'autres especes d'acacia

Variation in allele frequencies in the outcross pollen pool of Eucalyptus regnans F. Muell. throughout a flowering season

In a high-salt soluble fraction of the total protein from single seeds of Pinus radiata, up to 45 polypeptides were resolved on SDS-polyacrylamide gels. At least one-fifth of these polypeptides showed variation between seeds. In the 27,000--29,000 dalton region, two polypeptides were inherited as codominant alleles at a single locus and were shown to assort independently of another seed protein locus and three allozyme loci. A survey of 120 individuals from the five known native populations of P. radiata in California detected only the 27K and 29K alleles at the locus. In all populations, the 29K allele predominated, and the two island populations were monomorphic for the 29K allele. The 27 and 29 kdalton polypeptides were shown to have very similar amino acid sequences, and the allelic difference at this locus is most probably in the gene sequence for the polypeptide.