69 research outputs found

    Embryo rescue of cucumber (Cucumis sativus), muskmelon (C. melo) and some wild Cucumis species (C. anguria, C. zeyheri, and C. metuliferus)

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    Cucumis sativus is one of the most economically important crops of the Cucurbitaceae. Recent cucumber cultivars are susceptible to some serious diseases and pests, including downy mildew, powdery mildew, nematodes, and spider mites. Sources of resistance to these pathogens and pests were identified in some accessions of wild Cucumis species. One possible way of introducing these resistances into cucumber germplasm is interspecific hybridization. However, C. sativus is sexually incompatible with nearly all other Cucumis species, because of substantially different chromosome numbers, n = 7 in C. sativus versus n = 12 in C. melo and most wild Cucumis species. Overcoming this obstacle can be accomplished through the use of embryo rescue and/or ovule culture. Results of experiments using these methods, especially of embryo rescue of cucumber and selected wild Cucumis species after intra- and interspecific hybridization, are summarized in this paper. Various culture media and selected genotypes were tested in our experiments. Successful regeneration of mature embryos of some Cucumis spp. was observed on all types of media, and callus or sporadic plant formation from immature embryos and seeds occurred on media with coconut water and gibberellic acid

    Factors affecting protoplast isolation and cultivation of Cucumis spp.

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    Protoplasts of Cucumis anguria, Cucumis melo (3 accessions), Cucumis metuliferus and Cucumis sativus were isolated from leaves, growing apices, hypocotyls and calluses. Plants were cultured on 2 concentrations of sucrose. The effect of plant culture medium, explant age and explant type on protoplast viability were investigated. The protoplasts were cultured in 3 types of culture medium and at two temperatures. Optimal age range for protoplast isolation was 1-5 weeks depending on explant type and genotype. Viabilities ranging between 50 % and 80 % were obtained from all explants and genotypes. Increased concentration of sucrose had negative impact on viability of protoplasts. The highest level of regeneration achieved was callus, regenerated from leaf protoplasts of C. melo cv. ‘Charentais’ and C. melo ‘MR-1’. The lowest regeneration capability was observed in hypocotyls. Liquid LCM medium (B5 macro and microelements (1 g · l-1 CaCl2), B5 vitamins with 1g· l-1 myo-inositol, 2 mg· l-1 ascorbic acid, 0.8 mg· l-1 glycine, 20 mg· l-1 glutamine, 100 mg · l-1 casein hydrolysate, 70 g · l-1 mannitol, 10 g · l-1 sucrose, 5 g · l-1 glucose, 585 mg · l-1 MES, 5.37 μmol· l-1 NAA, 2.26 μmol· l-1 2,4-D, 2.22 μmol · l-1 BA) was optimal for protoplast regeneration. Agarose-solidified medium caused a decrease in the number of cell divisions (used in C. melo ‘PI 124112’). Cultivation at 25ºC resulted in a higher frequency of cell divisions (tested in C. metuliferus)

    Stretching the Rules: Monocentric Chromosomes with Multiple Centromere Domains

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    The centromere is a functional chromosome domain that is essential for faithful chromosome segregation during cell division and that can be reliably identified by the presence of the centromere-specific histone H3 variant CenH3. In monocentric chromosomes, the centromere is characterized by a single CenH3-containing region within a morphologically distinct primary constriction. This region usually spans up to a few Mbp composed mainly of centromere-specific satellite DNA common to all chromosomes of a given species. In holocentric chromosomes, there is no primary constriction; the centromere is composed of many CenH3 loci distributed along the entire length of a chromosome. Using correlative fluorescence light microscopy and high-resolution electron microscopy, we show that pea (Pisum sativum) chromosomes exhibit remarkably long primary constrictions that contain 3-5 explicit CenH3-containing regions, a novelty in centromere organization. In addition, we estimate that the size of the chromosome segment delimited by two outermost domains varies between 69 Mbp and 107 Mbp, several factors larger than any known centromere length. These domains are almost entirely composed of repetitive DNA sequences belonging to 13 distinct families of satellite DNA and one family of centromeric retrotransposons, all of which are unevenly distributed among pea chromosomes. We present the centromeres of Pisum as novel ``meta-polycentric'' functional domains. Our results demonstrate that the organization and DNA composition of functional centromere domains can be far more complex than previously thought, do not require single repetitive elements, and do not require single centromere domains in order to segregate properly. Based on these findings, we propose Pisum as a useful model for investigation of centromere architecture and the still poorly understood role of repetitive DNA in centromere evolution, determination, and function

    In Depth Characterization of Repetitive DNA in 23 Plant Genomes Reveals Sources of Genome Size Variation in the Legume Tribe Fabeae

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    The differential accumulation and elimination of repetitive DNA are key drivers of genome size variation in flowering plants, yet there have been few studies which have analysed how different types of repeats in related species contribute to genome size evolution within a phylogenetic context. This question is addressed here by conducting large-scale comparative analysis of repeats in 23 species from four genera of the monophyletic legume tribe Fabeae, representing a 7.6-fold variation in genome size. Phylogenetic analysis and genome size reconstruction revealed that this diversity arose from genome size expansions and contractions in different lineages during the evolution of Fabeae. Employing a combination of low-pass genome sequencing with novel bioinformatic approaches resulted in identification and quantification of repeats making up 55-83% of the investigated genomes. In turn, this enabled an analysis of how each major repeat type contributed to the genome size variation encountered. Differential accumulation of repetitive DNA was found to account for 85% of the genome size differences between the species, and most (57%) of this variation was found to be driven by a single lineage of Ty3/gypsy LTR-retrotransposons, the Ogre elements. Although the amounts of several other lineages of LTR-retrotransposons and the total amount of satellite DNA were also positively correlated with genome size, their contributions to genome size variation were much smaller (up to 6%). Repeat analysis within a phylogenetic framework also revealed profound differences in the extent of sequence conservation between different repeat types across Fabeae. In addition to these findings, the study has provided a proof of concept for the approach combining recent developments in sequencing and bioinformatics to perform comparative analyses of repetitive DNAs in a large number of non-model species without the need to assemble their genomes

    Symposium Report The Role of Protein-Protein and Protein-Membrane Interactions on P450 Function

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    ABSTRACT This symposium summary, sponsored by the ASPET, was held at Experimental Biology 2015 on March 29, 2015, in Boston, Massachusetts. The symposium focused on: 1) the interactions of cytochrome P450s (P450s) with their redox partners; and 2) the role of the lipid membrane in their orientation and stabilization. Two presentations discussed the interactions of P450s with NADPH-P450 reductase (CPR) and cytochrome b 5 . First, solution nuclear magnetic resonance was used to compare the protein interactions that facilitated either the hydroxylase or lyase activities of CYP17A1. The lyase interaction was stimulated by the presence of b 5 and 17a-hydroxypregnenolone, whereas the hydroxylase reaction was predominant in the absence of b 5 . The role of b 5 was also shown in vivo by selective hepatic knockout of b 5 from mice expressing CYP3A4 and CYP2D6; the lack of b 5 caused a decrease in the clearance of several substrates. The role of the membrane on P450 orientation was examined using computational methods, showing that the proximal region of the P450 molecule faced the aqueous phase. The distal region, containing the substrate-access channel, was associated with the membrane. The interaction of NADPH-P450 reductase (CPR) with the membrane was also described, showing the ability of CPR to "helicopter" above the membrane. Finally, the endoplasmic reticulum (ER) was shown to be heterogeneous, having ordered membrane regions containing cholesterol and more disordered regions. Interestingly, two closely related P450s, CYP1A1 and CYP1A2, resided in different regions of the ER. The structural characteristics of their localization were examined. These studies emphasize the importance of P450 protein organization to their function

    The peatland map of Europe

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    Based on the ‘European Mires Book’ of the International Mire Conservation Group (IMCG), this article provides a composite map of national datasets as the first comprehensive peatland map for the whole of Europe. We also present estimates of the extent of peatlands and mires in each European country individually and for the entire continent. A minimum peat thickness criterion has not been strictly applied, to allow for (often historically determined) country-specific definitions. Our ‘peatland’ concept includes all ‘mires’, which are peatlands where peat is being formed. The map was constructed by merging national datasets in GIS while maintaining the mapping scales of the original input data. This ‘bottom-up’ approach indicates that the overall area of peatland in Europe is 593,727 km². Mires were found to cover more than 320,000 km² (around 54 % of the total peatland area). If shallow-peat lands (< 30 cm peat) in European Russia are also taken into account, the total peatland area in Europe is more than 1,000,000 km2, which is almost 10 % of the total surface area. Composite inventories of national peatland information, as presented here for Europe, may serve to identify gaps and priority areas for field survey, and help to cross-check and calibrate remote sensing based mapping approaches
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