35 research outputs found

    Identification and mapping of a locus conferring plum pox virus resistance in two apricot-improved linkage maps

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    Sharka disease, caused by the plum pox virus (PPV), is one of the major limiting factors for stone fruit crops in Europe and America. In particular, apricot is severely affected suffering significant fruit losses. Thus, PPV resistance is a trait of great interest for the apricot breeding programs currently in progress. In this work, two apricot maps, earlier constructed with the F1 ‘Goldrich × Currot’ (G×C) and the F2 ‘Lito × Lito’-98 (L×L-98) populations, have been improved including 43 and 37 new simple sequence repeat (SSR) loci, respectively, to facilitate PPV resistance trait mapping. Screening of PPV resistance on the segregating populations classified seedling phenotypes into resistant or susceptible. A non-parametric mapping method, based on the Kruskal–Wallis (KW) rank sum test, was initially used to score marker–trait association, and results were confirmed by interval mapping. Contrary to the putative digenic model inferred from the phenotypic segregations, all significant markers for the KW statistic (P < 0.005) mapped in a unique region of ~21.0 and ~20.3 cM located on the upper part of the G1 linkage group in ‘G×C’ and ‘L×L-98’ maps, respectively. According to the data, PPV resistance is suggested to be controlled by at least one major dominant locus. The association between three SSRs distributed within this region and the PPV resistance was tested in two additional populations (‘Goldrich × Canino’ and ‘Lito × Lito’-00) and breeding program parents. The marker ssrPaCITA5 showed the highest KW value (P < 0.005) in all cases, pointing out its usefulness in marker-assisted selection.This research was supported by a grant from the Ministerio de Ciencia y Tecnología (AGL2004-04126-C02-02/AGR).Peer reviewe

    Genetic diversity, yield, and fruit quality of persimmon in the tropics

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    O objetivo deste trabalho foi estimar a diversidade genética, o rendimento e a qualidade de frutos de genótipos de caquizeiros cultivados nos trópicos, para selecionar materiais genéticos promissores. A extração de DNA foi realizada em folhas jovens de 19 genótipos de caqui. Para a caracterização pomológica, foram selecionados 15 genótipos. Para cada genótipo, 50 frutos foram colhidos pela manhã, no estágio de maturidade fisiológica, para determinar os seguintes parâmetros: características físico-químicas; e as variáveis produtivas número de frutos por planta, massa de matéria fresca média dos frutos, produtividade média e produtividade média estimada, em duas safras. Vinte marcadores SSR foram testados, dos quais 12 foram selecionados para avaliar a similaridade genética, o que permitiu a identificação de grupos distintos. O valor médio de diversidade genética encontrado foi 0,41, o que é indicativo de baixa diversidade entre os genótipos de caqui analisados. Os genótipos 'Guiombo', 'Iapar 125', 'Kakimel', 'Mikado RJ', 'Rama Forte Tardio' e 'Taubaté' apresentam alta produtividade. Os genótipos classificados como sendo de polinização constante adstringente ('Pomelo', 'Regina', 'Rubi' e 'Taubaté') e os classificados como sendo de polinização variante adstringente ('Rama Forte', 'Guiombo' e 'Cereja') são materiais com potencial para uso em programas de seleção e melhoramento genético, devido às suas excelentes características físico-químicas de fruta. A investigação por meio de marcadores moleculares é uma abordagem eficiente para estudar a diversidade genética de genótipos de caquizeiro cultivados nos trópicos.The objective of this work was to determine the genetic diversity, yield, and fruit quality of persimmon genotypes grown in the tropics, in order to select promising genetic materials. DNA extraction was performed on young leaves of 19 persimmon genotypes. For pomological characterization, 15 genotypes were selected. From each genotype, 50 fruit at the physiological maturity stage were harvested in the morning, in order to determine the following parameters: physicochemical characteristics; and the productive variables number of fruit per plant, average fruit fresh mass, average yield, and estimated average yield in two seasons. Twenty SSR markers were tested, out of which 12 were selected to evaluate genetic similarity, which allowed of the identification of distinct groups. The mean genetic diversity value found was 0.41, which is an indicative of low diversity among the analyzed persimmon genotypes. The 'Guiombo', 'Iapar 125', 'Kakimel', 'Mikado RJ', 'Rama Forte Tardio', and 'Taubaté' genotypes show a high yield. The genotypes classified as pollination-constant astringent ('Pomelo', 'Regina', 'Rubi', and 'Taubaté') and those classified as pollination-variant astringent ('Rama Forte', 'Guiombo', and 'Cereja') are potential materials for selection and genetic breeding programs due to their excellent fruit physicochemical characteristics. The investigation through molecular markers is an efficient approach to study the genetic diversity of persimmon genotypes grown in the tropics

    A peach germplasm collection for increasing the genetic diversity in European breeding programs

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    Trabajo presentado al VIII International Peach Symposium, celebrado en Matera (Italia) del 17 al 20 de junio de 2013.European breeding programs are hampered by the low intraspecific genetic diversity, which is due to the self-compatibility of this homozygous species along with the low number of genotypes introduced and thus used for breeding. In 2009, four research institutions which carried out peach breeding programs in Aragon, Catalonia, Valencia and Murcia, started a new peach germplasm collection worldwide aimed at enlarging the peach genetic diversity available for breeding. The plant material was introduced from germplasm collections located in China, Central Asia, Iran and the USA (National Germplasm Repository of Davis). Sanitary status was assessed by molecular diagnosis of known diseases caused by virus, viroid, bacteria and phytoplasm pathogens. Healthy plant material was grafted and maintained in quarantine conditions. The new germplasm collection was established in two places: Zaragoza as high chilling and Murcia as low chilling requirements. Pomological and molecular data were gathered and a public database constructed. The descriptors used were from the National Center for Genetic Resources from the INIA. Introduced budwood and seeds resulted in more than 250 new genotypes from 15 countries. The molecular analysis of a subset of the collection with 21 SSR markers evenly distributed in the genome resulted in a high number of alleles per SSR (mean A=9.5) and low observed heterozygosity (mean Ho=0.38). Variability was further assessed by geographic origin. Population structure analysis revealed the existence of 8 subpopulations explained, in some cases, by the geographic origin of the genotypes. As a result of the project a new database containing 95 accessions and 38 variables is available.Peer reviewe

    A Non-Targeted Approach Unravels the Volatile Network in Peach Fruit

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    Volatile compounds represent an important part of the plant metabolome and are of particular agronomic and biological interest due to their contribution to fruit aroma and flavor and therefore to fruit quality. By using a non-targeted approach based on HS-SPME-GC-MS, the volatile-compound complement of peach fruit was described. A total of 110 volatile compounds (including alcohols, ketones, aldehydes, esters, lactones, carboxylic acids, phenolics and terpenoids) were identified and quantified in peach fruit samples from different genetic backgrounds, locations, maturity stages and physiological responses. By using a combination of hierarchical cluster analysis and metabolomic correlation network analysis we found that previously known peach fruit volatiles are clustered according to their chemical nature or known biosynthetic pathways. Moreover, novel volatiles that had not yet been described in peach were identified and assigned to co-regulated groups. In addition, our analyses showed that most of the co-regulated groups showed good intergroup correlations that are therefore consistent with the existence of a higher level of regulation orchestrating volatile production under different conditions and/or developmental stages. In addition, this volatile network of interactions provides the ground information for future biochemical studies as well as a useful route map for breeding or biotechnological purposes

    Chromatin-associated regulation of sorbitol synthesis in flower buds of peach

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    [EN] Key message PpeS6PDH gene is postulated to mediate sorbitol synthesis in flower buds of peach concomitantly with specific chromatin modifications. Abstract Perennial plants have evolved an adaptive mechanism involving protection of meristems within specialized structures named buds in order to survive low temperatures and water deprivation during winter. A seasonal period of dormancy further improves tolerance of buds to environmental stresses through specific mechanisms poorly known at the molecular level. We have shown that peach PpeS6PDH gene is down-regulated in flower buds after dormancy release, concomitantly with changes in the methylation level at specific lysine residues of histone H3 (H3K27 and H3K4) in the chromatin around the translation start site of the gene. PpeS6PDH encodes a NADPH-dependent sorbitol-6-phosphate dehydrogenase, the key enzyme for biosynthesis of sorbitol. Consistently, sorbitol accumulates in dormant buds showing higher PpeS6PDH expression. Moreover, PpeS6PDH gene expression is affected by cold and water deficit stress. Particularly, its expression is up-regulated by low temperature in buds and leaves, whereas desiccation treatment induces PpeS6PDH in buds and represses the gene in leaves. These data reveal the concurrent participation of chromatin modification mechanisms, transcriptional regulation of PpeS6PDH and sorbitol accumulation in flower buds of peach. In addition to its role as a major translocatable photosynthate in Rosaceae species, sorbitol is a widespread compatible solute and cryoprotectant, which suggests its participation in tolerance to environmental stresses in flower buds of peach.This work was funded by the Instituto Nacional de Investigacion y Tecnologia Agraria y Alimentaria (INIA)-FEDER (RF2013-00043-C02-02) and the Ministry of Science and Innovation of Spain (AGL2010-20595). 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    Chilling-Dependent Release of Seed and Bud Dormancy in Peach Associates to Common Changes in Gene Expression

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    Reproductive meristems and embryos display dormancy mechanisms in specialized structures named respectively buds and seeds that arrest the growth of perennial plants until environmental conditions are optimal for survival. Dormancy shows common physiological features in buds and seeds. A genotype-specific period of chilling is usually required to release dormancy by molecular mechanisms that are still poorly understood. In order to find common transcriptional pathways associated to dormancy release, we analyzed the chilling-dependent expression in embryos of certain genes that were previously found related to dormancy in flower buds of peach. We propose the presence of short and long-term dormancy events affecting respectively the germination rate and seedling development by independent mechanisms. Short periods of chilling seem to improve germination in an abscisic acid-dependent manner, whereas the positive effect of longer cold treatments on physiological dwarfing coincides with the accumulation of phenylpropanoids in the seed

    Cost-effective and time-efficient molecular assisted selection for ppv resistance in apricot based on ParPMC2 allele-specific PCR

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    Plum pox virus (PPV) is the most important limiting factor for apricot (Prunus armeniaca L.) production worldwide, and development of resistant cultivars has been proven to be the best solution in the long-term. However, just like in other woody species, apricot breeding is highly time and space demanding, and this is particularly true for PPV resistance phenotyping. Therefore, marker-assisted selection (MAS) may be very helpful to speed up breeding programs. Tightly linked ParPMC1 and ParPMC2, meprin and TRAF-C homology (MATH)-domain-containing genes have been proposed as host susceptibility genes required for PPV infection. Contribution of additional genes to PPV resistance cannot be discarded, but all available studies undoubtedly show a strong correlation between ParPMC2-resistant alleles (ParPMC2res) and PPV resistance. The ParPMC2res allele was shown to carry a 5-bp deletion (ParPMC2-del) within the second exon that has been characterized as a molecular marker suitable for MAS (PMC2). Based on this finding, we propose here a method for PPV resistance selection in apricot by combining high-throughput DNA extraction of 384 samples in 2 working days and the allele-specific genotyping of PMC2 on agarose gel. Moreover, the PMC2 genotype has been determined by PCR or by using whole-genome sequences (WGS) in 175 apricot accessions. These results were complemented with phenotypic and/or genotypic data available in the literature to reach a total of 325 apricot accessions. As a whole, we conclude that this is a time-efficient, cost-effective and straightforward method for PPV resistance screening that can be highly useful for apricot breeding programs
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