应用SSR标记进行部分黄肉桃种质鉴定和亲缘关系分析

以116份黄肉桃种质和19份其它桃或桃近缘种种质为试材,利用定位于李属参考图谱上的SSR标记,进行遗传多样性评价及亲缘关系分析。SSR扩增结果表明,筛选出的28对SSR引物共扩增出206个等位基因,其中多态性等位基因159个（占76.56%）。聚类结果表明,在相似系数为0.82时,黄肉桃资源在聚类图上呈两组：美洲、欧洲和亚洲育成黄桃品种聚为一组（Ⅰ）,中国地方黄桃品种中唯‘西安杏瓤桃’和‘天津黄肉’出现在这一组;来源于云南、华北、西北地区的中国地方黄桃品种聚为另一组（Ⅱ）。在相似系数为0.87时,育成黄桃品种（Ⅰ）分为8个亚组,美洲育成品种分布在所有8个亚组中,欧洲育成品种分布在Ⅰ-2、Ⅰ-3和Ⅰ-4亚组,而亚洲育成品种仅分布在Ⅰ-3和Ⅰ-4亚组;亲本相同的育成品种在聚类图中临接或出现在较近的位置,育成品种的聚类结果与品种的系谱关系基本吻合。在相似系数为0.87时,中国地方黄桃品种分为7个亚组,西南黄桃和西北黄桃存在一定的组群界限,来自西南的黄桃地方资源主要分布在Ⅱ-1和Ⅱ-5亚组,而来自西北的黄桃地方品种主要出现在Ⅱ-2、Ⅱ-4和Ⅱ-7亚组。品种群的聚类结果表明,亚洲育成品种与美洲育成品种间亲缘关系最近,其次为欧洲育成品种;中国地方黄桃品种与育成品种间亲缘关系较远。     

Assessment of genetic relationships among 29 introduced and 49 local sweet cherry accessions in Turkey using AFLP and SSR markers

Summary

The characterisation of sweet cherry (Prunus avium L.) genetic resources in Turkey may help to increase their use in breeding programmes worldwide, as Turkey is the centre of origin of sweet cherry. Amplified fragment length polymorphism (AFLP) and simple sequence repeat (SSR) markers were therefore used to analyse genetic diversity among a total of 78 local and introduced sweet cherry cultivars. Four AFLP primer combinations, and six SSR primer pairs for sweet cherry were used for genetic diversity analysis. A genetic similarity matrix was calculated using the combined data from AFLP and SSR analyses with simple matching coefficient. Genetic similarities among the sweet cherry genotypes studied were higher than 42%. No two accessions had an identical AFLP and SSR marker profile, indicating that all 78 genotypes were unique. An UPGMA dendrogram, based on the similarity matrix, revealed 18 separate Groups at or above the 70% similarity level. While some Groups consisted of both introduced and local genotypes, other Groups had only local genotypes. This result suggests that there was broad genetic diversity among the local Turkish sweet cherry genotypes, which was not present in the introduced sweet cherry accessions. The genetic variation present in local Turkish sweet cherry genotypes may be useful for future breeding programmes. We found that the use of both SSR and AFLP marker systems was effective for distinguishing between genetically-close sweet cherry genotypes. These marker systems can be used to complement pomological and morphological markers during the characterisation and identification of sweet cherry genotypes.     

Assessment of genetic diversity in common bean (Phaseolus vulgaris L.) germplasm using amplified fragment length polymorphism (AFLP)

AFLP technique was applied to assess genetic diversity among 44 common bean accessions that included 6 exotic accessions, 15 Indian land races and 23 released varieties. Eight AFLP primer pairs were used that produced 820 products of which 698 were polymorphic (85.12%). Wide variations were observed among all the accessions for the number of amplification products, percent polymorphism and average polymorphism information content (PIC). The Jaccard's similarity indices (J) based on the AFLP profiles were subjected to UPGMA cluster analysis. The dendrogram generated revealed seven major groups. Seventeen out of 23 released varieties were restricted to clusters VI and VII. The value of r = 0.934 in Mantel's test for cophenetic corrlelation applied to the cluster analysis indicated the high fitness of the accessions to a group. The germplasm used in the present study had narrow genetic base, although moderate to high genetic diversity was observed. The details of diversity analysis and the potential use of Indian common bean accessions in common bean breeding programme are provided in the present study.     

Morphological and molecular analysis of genetic diversity in jackfruit

Summary

RAPD markers were used to estimate genetic diversity in 12 high-yielding jackfruit (Artocarpus heterophyllus Lamk.) accessions obtained from different locations in southern India. Marker data were compared with morphological data obtained over three successive seasons. PCR-amplifiable DNA was isolated using the CTAB method and 171 amplified fragments were obtained using 23 random primers. The genetic dissimilarity matrix was calculated based on Squared Euclidian Distances, which revealed a maximum genetic distance of 7.9% between a clone of ‘Mottavarica’ (‘M₀’), and ‘Chandrahalasu’ from distant locations, while the minimum genetic distance (5%) was between the genotypes (‘M₀’) and ‘Kerala’, indicating their similar geographical origin. Ward's method of cluster analysis grouped all individuals on the dendrogram into two major clusters according to their geographical location. The present study showed low-to-moderate genetic diversity among the 12 jackfruit accessions, which will assist in the identification and management of jackfruit germplasm for breeding purposes.     

Genetic characterization of different demes in Prunus persica revealed by RAPD markers

DNAs of 180 accessions in 10 demes in Prunus persica were amplified with twenty-two, 10-base primers selected from 200 arbitrary primers using Randomly Amplified Polymorphic DNA (RAPD) technology. One hundred and eighty loci were observed and recorded. With statistical analyses of the data from the study, genetic diversity of the demes was expressed as follow: yellow peach group > honey peach group > flat peach group > red leaf peach group > crisp peach group > bitao group and juicy peach group > nectarine group > shouxingtao group > weeping peach group. Genetic variations among and within groups by AMOVA analyses were 11.9, 88.1%, respectively. Demes clustered by UPGMA modified from NEIGHBOR procedure of PHYLIP Version 3.5, the edible peaches of which were combined as a section, while the ornamental species were classified into separate sections. Through analyses of genetic diversity and genetic structure, the results could provide molecular biological evidence for conservation and utilization of P. persica germplasm.     

我国冬桃资源的历史探析

对我国冬桃的历史记载进行整理与考证。冬桃是桃在古代驯化过程中最早形成的栽培类型，它的存在至少有３ ０００ 年以上的历史。我国冬桃品种繁多，性状各异，但都不同程度地带有原始类型的属性，它们对于研究桃的进化和品种改良具有重要价值，是一类宝贵的遗传资源。     

Inter- and intra-varietal analysis of three Olea europaea L. cultivars using the RAPD technique

Summary

Characterization and selection of olive clones for the production of olive oil is essential in Portugal because of its profitable exploitation. “Moura-Serpa” is the most important Portuguese region for the production of olive oil relying on three cultivars for oil quality. These are ‘Galega Vulgar’, ‘Cordovil de Serpa’ and ‘Verdeal Alentejana’. Therefore, it is of great importance to guarantee the varietal certification of the young trees and the establishment of new orchards. Random Amplified Polymorphic DNA (RAPD) technique was used to characterize these three cultivars. Analysis started using twenty primers that allowed us to distinguish the three cultivars and to select a reduced set of primers. The selected primers were used for inter- and intra-varietal analysis and for establishing a profiling system to assay genetic diversity in other olive cultivars. The method has the potential for use in varietal certification and breeding programmes that need to analyse a high number of samples.     

SSR fingerprinting Chinese peach cultivars and landraces (Prunus persica) and analysis of their genetic relationships

Thirty-two Chinese peach landraces/cultivars, a major subset of the core Chinese peach collection, were fingerprinted using seven pairs of SSR primers to assess their genetic diversity and relatedness. The seven primer pairs detected eight loci and revealed an allele richness of 3.125 (average alleles per locus), an expected heterozygosity (He) of 0.450, and a Shannon index of 0.728 among the landraces/cultivars. This level of genetic diversity is lower compared to other fruit trees and Prunus congenus species (cherry and apricot), but it is comparable to previous reports in peaches. A greater level of genetic diversity was observed in landraces than in cultivars, indicating that peach landraces are valuable for germplasm collection. All cultivars and landraces, except two, were unambiguously identified based on multi-locus genotypes. Eight unique alleles were detected among this group of Chinese peaches. UPGMA clustering analysis separated the 32 cultivars/landraces into two distinct groups, which is generally in accordance with the known pedigree information. The results provide accurate genetic information for defined acquisition policy in the repositories, improving the integrity and efficiency of germplasm management and giving evidences for protection of breeder's intellectual rights.     

Molecular diversity of Chinese Cucurbita moschata germplasm collections detected by AFLP markers

Cucurbita moschata is an important vegetable crop. Although a total of 1032 landraces of C. moschata are maintained in China, little is known about their genetic diversity. Molecular characterization is needed to facilitate the use of this C. moschata germplasm collection in breeding. Seventy-four Chinese accessions and 15 accessions from other countries were selected for evaluation based upon variation in fruit traits and geographical origin of molecular diversity with AFLP analysis. Nine pairs of EcoRI/MseI primers produced 500 fragments, of which 75.57% were polymorphic, indicating a high degree of diversity. The accessions from China were classified into two clusters, which were clearly differentiated from the accessions originating from Mexico, Guatemala, Honduras, and Ecuador. Chinese group genetically more closely related to other Asian countries group (India and Japan). In general, the accessions from the Americas had a greater number of unique loci than those from China. The differences are probably due to a limited number of introductions and genetic drift. The Americas are the center of origin of C. moschata and therefore more diverse. With AFLP analysis, the accessions did not clearly group according to fruit shape; however, sub-clusters exist in acorn- and dumbbell-shaped accessions. The assessment of genetic distance, along with some unique traits among the different genotypes, could be useful in further genetic studies and the selection of the most adequate accessions for use in breeding programs.     

Genetic diversity in fruiting-mei,apricot, plum and peach revealed by AFLP analysis

Summary

High-throughput amplified fragment length polymorphism (AFLP) analysis, employing a two-dye automated DNA sequencer, was used to genotype accessions of four important Prunus spp. fruit crops in China, fruiting-mei (P. mume), apricot (P. armeniaca), plum (P. salicina, and P. ussuriensis) and peach (P. persica). Nine primer pairs generated a total of 2,089 AFLP bands, of which 94.4% were polymorphic. Levels of polymorphism and the genetic relationships among the crops were studied.The fixation index (F_st) of the four different fruit trees ranged from 0.53 – 0.82, and the average genetic diversity (AGD) in these species ranged from 3.2% to 12.8%. These four stone fruit species could be clustered into four clear groups on a phylogenetic tree based on bootstrap analysis. Phylogenetically, fruiting-mei was shown to be closest to apricot and most distant from peach.     

Assessing Rosa persica genetic diversity using amplified fragment length polymorphisms analysis

The genetic diversity among 128 Iranian Rosa persica (R. persica) accessions in the different populations was analyzed. Amplified fragment length polymorphisms (AFLP) technique was used to produce 171 polymorphic fragments. The number of polymorphic loci ranged from 101 to 147 and the polymorphism information content (PIC) varied from 0.289 to 0.073, with an average of 0.16. This shows extreme variability and genetic diversity among the studied R. persica populations. An indirect estimate of the number of migrants per generation (Nm = 0.376) indicated that gene flow was relatively low among populations of the species. Cluster analysis using the UPGMA method grouped all accessions into six clusters. The results did not show relative agreement with the genotypes’ region of origin. Based on an analysis of molecular variance, 48% of the genetic variation of R. persica was within population and 52% was among populations. The present analysis revealed that Iranian R. persica genotypes are highly variable and genetically distinct from their origins. The apparent unique nature of the R. persica genotypes revealed by our results supports the case for the implementation of more intense characterization and conservation strategies, and provides useful information to address breeding programmes and germplasm resource management in Rosa spp.     

Starch granule size variation and relationship with tuber dry matter content in heritage potato varieties

Heritage potato varieties in Canada are historic old varieties collected from Canada and various countries before the formal establishment of the Canadian plant variety registration system and may be a valuable gene resource for beneficial traits in potato breeding and bioproducts development. Greater evaluation is the key for the enhanced use of these materials. It is unknown how much variation of starch granules occurs among Canadian heritage potato varieties. We analyzed the starch granule size of 14 potato heritage varieties held in the Canadian Plant Gene Resources collection over 2 years using a squeezed juice and microscopic method recently developed at the Potato Research Centre. The varieties demonstrated considerable variation in starch granule size and shape. The granules showed average lengths ranging from 18 μm in the variety Congo to 32 μm in ‘Russet Burbank’. The largest single granule measured from 64 μm in ‘Congo’ to 91 μm in ‘Crotte d’Ours.’ The granule sizes of the varieties showed a very high correlation (r = 0.975, P < 0.0001) between years. This high reproducibility suggests the existence of genetic factors in determining starch granule size. We also found that the starch granule size is positively correlated with tuber dry matter (in terms of specific gravity) in these heritage potatoes. The results demonstrated reproducible genotypic variation for starch granule size and shape in tubers with a significant correlation to tuber dry matter in these heritage potato varieties, and offers the possibility for and agronomic relevance of genetic modification of starch granules through selective breeding.     

Molecular characterization of Miraflores peach variety and relatives using SSRs

Some traditional peach varieties, originated from the region of Aragón (Spain), were analysed by SSRs (simple sequence repeats). The aim of this research was to characterize 19 clones related to Miraflores variety, with unknown pedigrees, to assess their genetic diversity and to elucidate their possible relationships with 10 traditional peach varieties. Twenty SSR primer pairs with high levels of polymorphism, which have been previously developed for peach, were used in this study. A total of 46 alleles were obtained for all the microsatellites studied, ranging from one to six alleles per locus, with a mean value of 2.3 alleles per locus. Fourteen SSRs were polymorphic in the set of varieties studied and permitted to distinguish 16 different genotypes out of the 30 initially studied, although fourteen ‘Miraflores’ clones showed identical gel profiles. The genetic distance matrix was used to construct neighbor joining cluster and to perform principal coordinate analysis which allowed the arrangement of all the genotypes according to their genetic relationships. The genetic relationships among these traditional peach varieties, and in particular among ‘Miraflores’ clones are discussed. The obtained results confirm that microsatellite markers are very useful for these purpose.     

Variation and correlation analysis of polyphenolic compounds in Malus germplasm

To clarify the variation and characteristics of polyphenolic compounds in Malus germplasm, and also to provide a theoretical basis for the application of apple landraces in China, polyphenolic compounds and concentrations were analysed in 103 Malus accessions from China using ultra performance liquid chromatography and liquid chromatography-mass spectrometry. The apple landraces of North China, which should have undergone more artificial selection than those of Northwest China and Northeast China, are used as table fruit, or as parents for breeding table varieties with high polyphenolic concentrations from. Wild species have been appropriated as parents for historical hybridisation of new genetic resources with high polyphenolic concentrations. The apple landraces ‘Bandayulenggunzi #1’ and ‘Duanzhigunzi’ possess the greatest concentrations of total polyphenols detected, and so could be used as table fruit by consumers directly, or as parents for breeding varieties with high polyphenolic concentrations from by breeders. The apple landraces originating from North China, Northwest China and Northeast China, are significantly separated by linear discriminant analysis (LDA), and the wild species and apple landraces are evidently discriminated by LDA as well. Hierarchical cluster analysis of polyphenolic compounds of Malus accessions resulted in clusters derived from closely-related biochemical pathways.     

Characterisation of novel simple sequence repeat (SSR) markers for melon (Cucumis melo L.) and their use for genotype identification

Summary

The objectives of this study were to provide a set of useful simple sequence repeat (SSR) markers, to characterise them, and to demonstrate their ability to detect polymorphisms across diverse genotypes of melon. A total of 183 SSR markers were developed in melon from libraries enriched for (CA)_n, (CT)_n, (AAG)_n, and (ATG)_n repeats. The efficiency of marker development was highest in the CT library. The efficiencies of the CA, AAG, and ATG libraries were similar, and approx. 60% of that of the CT library. Dinucleotide motifs were observed more frequently than trinucleotide motifs. Approx. 50% of CA/TG motifs and approx. 30% of CT/AG motifs exhibited a repeat number greater than ten, while most other motifs showed a repeat number of less than ten. Fifty primer pairs were selected at random and used to evaluate polymorphisms among 19 melon accessions representing seven varieties. All 50 markers were amplified successfully in the majority of accessions, and 42 markers were polymorphic among the 19 melon accessions. All polymorphic markers could detect variation between at least two accessions belonging to the same variety, with polymorphic information content values ranging from 0.10 - 0.96. The SSR markers developed were variable and transferable and will be valuable molecular tools in melon breeding programmes.     

SSR-based DNA fingerprints reveal the genetic diversity of Sicilian olive (Olea europaea L.) germplasm

Summary

Twelve published simple sequence repeat (SSR; microsatellite) markers, belonging to the ssrOeUA-DCA, GAPU and UDO series, were tested in a panel of 46 accessions of olive germplasm belonging to 30 unique cultivars collected in seven Provinces of Sicily. Four well-known reference olive cultivars were also added. The analysis was carried out on an automatic capillary sequencer using fluorescent dyes, and fragment sizes were determined using internal standards. The results allowed us to rank the SSRs assayed according to their information content and reproducibility. Up to 115 alleles were identified (119, if those unique to sport mutations were included), the frequency of which allowed genetic relationships among accessions to be investigated. The probability that two unrelated genotypes displayed the same SSR pattern at all loci examined was calculated to be as low as 1.18 10^–11. Sixteen accessions were identified as synonyms. Of these, eight matched perfectly with another accession at all SSR loci examined. The others showed one or two allelic differences from the reference accession. These were interpreted as mutations. Otherwise, all accessions were clearly separated from each other. Two likely parentages were also identified (‘Giarfara’ = ‘Nocellara del Belice’

‘Cacaridduni’; and ‘Pizzo di Corvo’ = ‘Nocellara Etnea’ ‘Tonda Iblea’). The genetic diversity of the pool represented by the unique accessions was very high, reflecting the richness of the olive germplasm accumulated in Sicily. A database of the accessions is available to the scientific community (http://www.unipa.it/germolive/ssr.html) to facilitate comparisons of data.     

Further Work on Plant Injection for Diagnostic and Curative Purposes

Summary

Randomly Amplified Polymorphic DNA (RAPD) markers were used to evaluate genetic similarity and inter-relationship among31 acid citrus species and cultivars, including sour oranges (six accessions); ‘Yuzu’ (four accessions) andits relatives (21 accessions). Out of the 60 decamer primers screened, 27 were selected which produced 108 markers; 76 of which were polymorphic. Species or cultivar-specific RAPD markers were also found. A dendrogram based on genetic distance implied that sour oranges were very distinct from ‘Yuzu’ and its relatives. ‘Yuzu’ accessions were very closely linked to each other, however; for the other specimens genetic polymorphism could easily be detected by RAPDs and the genetic variation between accessions was quite high and revealed their different origins. In this study some RAPDs allowed the distinction of very close cultivars, for instance ‘Kabosu’ from ‘Aka kabosu’.     

短低温桃和油桃育种进展

从短低温桃、油桃品种的价值、育种历史、特点、遗传背景、主要育种目标和优良品种介绍等方面概述了短低温桃品种的研究进展，提出了我国短低温桃育种的目标。     

Recent trends in muskmelon (Cucumis melo L.) research: an overview

Muskmelon is a warm season old-world cucurbit species which belongs to family Cucurbitaceae. It has served as a wonder crop since ancient times, as the leaves and seeds of it are used to treat hematoma, and the stems to reduce hypertension. For decades, it has played key roles in the field of plant molecular biology and plant physiology, serving as an excellent model plant for investigating the phenomenon of sex determination and ripening processes. Elite varieties of melons carrying the wide potential to serve as more demanding to end user and against tolerance to drought condition and inferior lands, or diseases have been developed. Plant-breeding methods (conventional or molecular breeding) and transgenic technology are the only tools left, with which we can deploy to regenerate the elite varieties in melon fruits to meet the global demand for next decades. The development of plant biotechnological tools for melons offers the prospect to develop new varieties, more rapidly, avoiding natural genetic barriers. The use of these methods has extended to increase the genetic diversity by somatic hybridisation or gene transfer and to optimise conventional breeding programmes. In this review, we have focused on the status of crop improvement in muskmelon since a period of time for different traits like quality improvement, sex expression as well as resistances against biotic and abiotic stresses.     

Genetic divergence among gerbera accessions evaluated by RAPD

Genetic diversity was evaluated by RAPD markers and morpho-agronomic characters for a total of 42 accessions of Barberton daisy (Gerbera jamesonii) consisting of 29 commercial and 13 wild accessions. A total of 74 polymorphic bands were obtained employing a set of 12 primer pairs. The average genetic similarity coefficient for the 42 accessions, evaluated by Jaccard index was 0.55 ranging from 0.28 to 1.00. The genetic structure found among Barberton daisy accessions was evaluated by hierarchic classification analyses and UPGMA modeling, revealing six clusters of genotypes where two of them include the wild accessions and the remaining four including commercial material, except for wild genotype number 9. Shannon (H′) index was calculated using the molecular markers to investigate the genetic variation among the Gerbera accessions and showed higher values for the commercial cluster in comparison to the values obtained for the individuals from the non-commercial cluster, namely 0.34 versus 0.27, respectively. Therefore, both calculated indices (Jaccard and Shannon) indicated the presence of higher genetic variation among commercial accessions in comparison to the cluster representing non-commercial accessions, suggesting that genetic breeding programs may focus on commercial accessions to recombine interesting genotypes with commercially important and marketing-desired characteristics.