QTL mapping of volatile compounds in ripe apples detected by proton transfer reaction-mass spectrometry

The availability of genetic linkage maps enables the detection and analysis of QTLs contributing to quality traits of the genotype. Proton Transfer Reaction Mass Spectrometry (PTR-MS), a relatively novel spectrometric technique, has been applied to measure the headspace composition of the Volatile Organic Compounds (VOCs) emitted by apple fruit genotypes of the progeny ‘Fiesta’ × ‘Discovery’. Fruit samples were characterised by their PTR-MS spectra normalised to total area. QTL analysis for all PTR-MS peaks was carried out and 10 genomic regions associated with the peaks at m/z = 28, 43, 57, 61, 103, 115 and 145 were identified (LOD > 2.5). We show that it is possible to find quantitative trait loci (QTLs) related to PTR-MS characterisation of the headspace composition of single whole apple fruits indicating the presence of a link between molecular characterisation and PTR-MS data. We provide tentative information on the metabolites related to the detected QTLs based on available chemical information. A relation between apple skin colour and peaks related to carbonyl compounds was established. The two authors contributed equally to this work.     

A molecular marker linked to the Prv1 gene that confers resistance to Papaya ringspot virus-type W in melon

Papaya ringspot virus‐type W (PRSV‐W) is the most prevalent and important viral pathogen of cucurbits in Brazil. It can be effectively controlled by the incorporation of genetic resistance into susceptible melon cultivars. The present study identified amplified fragment length polymorphic (AFLP) markers linked to the PRSV‐W resistance Prv¹ allele. The susceptible yellow‐fleshed melon‐breeding line AF426^prv1 and its nearly isogenic‐resistant line AF426^Prv1, which carries the Prv¹ allele resident in the Indian cantaloupe U.S. Plant Introduction (PI) 180280, were screened for AFLP marker polymorphisms. Of 30 251 AFLP loci, only three were polymorphic between the nearly isogenic lines. Segregation analyses for these three polymorphic markers and the Prv¹ allele using a BC₁ population of 197 plants indicated close linkage (0.5% recombination frequency) between marker EK190 (HindIII‐CGA and MseI‐GTG; 190 bp) and Prv¹. Thus, EK190 might be a useful marker in breeding programmes aiming to develop melon cultivars resistant to PRSV‐W. The other two markers are closely linked to each other, but distantly linked to Prv¹.     

Genetical Studies on the Mode of Inheritance and Localization of the amo1 (High Amylose) Gene in Barley

In the high amylose starch mutant ‘Glacier AC38’, a single recessive gene designated amo1 is responsible for an amylose content of up to 45%. A rapid technique was established in order to evaluate the amylose/amylopectin ratio in half kernels. To localize this gene, crosses with multiple marker lines and trisormes were conducted. In addition, RFLP markers were used to determine their mapping distance to amo1. Two markers are located 2 cM and 7 cM, respectively, from amo1 on chromosome 5S (1HS). The relationship between the wx and amo1 genes was also examined and the role of the amo1 gene in starch synthesis is discussed.     

Molecular markers linked to rhizomania resistance in sugar beet, Beta vulgaris, from two different sources map to the same linkage group

Rhizomania, one of the most important diseases of sugar beet, is caused by beet necrotic yellow vein virus, a Furovirus vectored by the fungus Polymyxa betae Keskin. Reduction of the production losses caused by this disease can only be achieved by using tolerant cultivars. The objective of this study was the identification and mapping of random amplified polymorphic DNA (RAPD) markers linked to a rhizomania resistance gene. The RAPD markers were identified using bulked segregant analysis in a segregating population of 62 individuals derived by intercrossing plants of the resistant commercial hybrid GOLF, and the resistance locus was positioned in a molecular marker linkage map made with a different population of 50 GOLF plants. The resistance locus, Rr1, was mapped to linkage group III of our map of Beta vulgaris L. ssp. vulgaris, which consisted of 76 RAPDs, 20 restriction fragment length polymorphisms (RFLPs), three sequence characterized amplified regions (SCARs) and one sequence tagged site (STS). In total, 101 molecular markers were mapped over 14 linkage groups which spanned 688.4 cM with an average interval length of 8.0 cM. In the combined map, Rr1 proved to be flanked by the RAPD loci RA411₁₈₀₀ and AS7₁₁₀₀ at 9.5 and 18.5cM, respectively. Moreover, in our I₂ population, we found that a set of markers shown by Barzen et al. (1997) to be linked to the ‘Holly’ type resistance gene was also linked to the ‘GOLF’-type resistance gene. These results appeared to indicate that the rhizomania resistance gene present in the GOLF hybrid could be the same gene underlying resistance in ‘Holly’-based resistant genotypes. Two other explanations could be applied: first, that two different alleles at the same locus could have been selected; second, that two different genes at two different but clustered loci underwent the selection process.     

Relation in the inheritance of resistance to Pseudoperonospora cubensis rost and Sphaerotheca fuliginea poll. in cucumber (Cucumis sativusl. L.)

Summary Among the genes for resistance against Sphaerotheca fuliginea, the gene s for resistance of the hypocotyl is linked to or identical with gene p for resistance to Pseudoperonospora cubensis. This gene s is present in the cultivars Ashley, Poinsett, Natsufushinari, Pixie, Taipei and in accessions PI 179676. PI 212233 and PI 234517.Although gene s initially brings about some resistance of the true leaf, it appears that when s is present. other genes are necessary for complete resistance to S. fuliginea.     

Recurrent selection in autogamous species under forced random mating

Summary Artificial selection in autogamous species is investigated applying standard algebraic techniques to conventional self-pollinating breeding systems as well as to recurrent cross-pollinating ones for both one and two-locus models. More than two loci are considered by means of computer simulations. Allelic and non-allelic genotypic interactions as well as genes with a large effect are considered whenever possible. The overall picture shows a clear superiority of recurrent selection systems over self-pollinating breeding systems when negative linkage disequilibrium is either present or generated as is expected in actual breeding populations. When epistatic interaction enhances the selective advantage of new recombinants the superiority of recurrent selection is even greater.     

Inheritance of zucchini yellow mosaic virus resistance in Cucumis melo L.

Summary Resistance to zucchini yellow mosaic virus has been found in the muskmelon line PI 414723 from India. This resistance is effective against the ZYMV strains E15 and 1318 belonging respectively to the NF and F pathotypes. Resistance to E15 (no vein clearing and yellowing symptoms) is governed by one dominant gene (symbol Zym) according to segregations observed in F₁, F₂ and BC₁ progenies. This gene is epistatic dominant over Fn, which induces wilting and necrosis after inoculation with F pathotype. Linkage studies suggest that Zym inherits independently from Fom-1, Fom-2, Vat, Wmv and Fn but is linked with a (13.1 ±2.4 units).     

Molecular genetic mapping of peach

Summary A project to develop a linkage map of the peach (Prunus persica) genome is underway using an F2 population segregating for several morphological characters and pest resistance e.g., nectarine (g), weeping shape (pl) and aphid resistance (Rml). The RAPID technique was used to analyse 270 plants. Linkage analysis of the F2 population was performed using the MAPMAKER software. Eight linkage groups were established and RAPID markers flanking thepl gene were found.     

Allozymes and growth habit of Aegilops tauschii: genetic control and linkage patterns

Aegilops tauschii line of spring type growth habit with theearliest heading among all the VIR world germplasm collection of thisspecies was crossed with three Ae. tauschii lines of winter type growthhabit with low, intermediate and the highest vernalization requirement. 12enzyme loci were involved in genetic analysis. The growth habit was foundto be encoded by single codominant major gene, Vrn-D2. Thefollowing linkages were found: Est5 – Nadhd2 in chromosome 3, Vrn-D2 – Aco2 – Cat2 and Pgm – Nadhd1 in chromosome 4, Est2 – Got2 in chromosome 6.     

Cultivar identification and genetic map of mango (Mangifera indica)

Amplified Fragment Length Polymorphism (AFLP) information was used for identification of mango (Mangifera indica L.) cultivars, for studying the genetic relationship among 16 mango cultivars and seven mango rootstocks and for the construction of a genetic linkage map. Six AFLP primer combinations produced 204 clear bands and on the average 34 bands for each combination. The average Band-Sharing between cultivars and rootstocks was 83% and 80%, respectively. The average Band-Sharing for mango is 81%. The probability of obtaining a similar pattern for two different mango cultivars and rootstocks is 6 × 10⁻³and 2 × 10⁻³, respectively. A preliminary genetic linkage map of the mango genome was constructed, based on the progeny of a cross between ‘Keitt’ and ‘Tommy-Atkins’. This linkage map consists of 13 linkage groups and covers 161.5 cm defined by 34 AFLP markers. This revised version was published online in August 2006 with corrections to the Cover Date.