79 research outputs found
Location of chlorogenic acid biosynthesis pathway and polyphenol oxidase genes in a new interspecific anchored linkage map of eggplant
© Gramazio et al.; licensee BioMed Central. 2014. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated
Crop wild relatives of the brinjal eggplant ( Solanum melongena ): Poorly represented in genebanks and many species at risk of extinction
This is the publisher's Early View pdf without final pagination .© 2016 Botanical Society of America. This is an open access article, available to all readers online, published under a creative commons license. The attached file is the published version of the article
Characterising the CI and CI-like carbonaceous chondrites using thermogravimetric analysis and infrared spectroscopy
The CI and CI-like chondrites provide a record of aqueous alteration in the early solar system. However, the CI-like chondrites differ in having also experienced a late stage period of thermal metamorphism. In order to constrain the nature and extent of the aqueous and thermal alteration, we have investigated the bulk mineralogy and abundance of H2O in the CI and CI-like chondrites using thermogravimetric analysis and infrared spectroscopy.
The CI chondrites Ivuna and Orgueil show significant mass loss (28.5–31.8 wt.%) upon heating to 1000 °C due to dehydration and dehydroxylation of abundant phyllosilicates and Fe-(oxy)hydroxides and the decomposition of Fe-sulphides, carbonates and organics. Infrared spectra for Ivuna and Orgueil have a prominent 3-μm feature due to bound −OH/H2O in phyllosilicates and Fe-(oxy)hydroxides and only a minor 11-μm feature from anhydrous silicates. These characteristics are consistent with previous studies indicating that the CI chondrites underwent near-complete aqueous alteration. Similarities in the total abundance of H2O and 3 μm/11 μm ratio suggest that there is no difference in the relative degree of hydration experienced by Ivuna and Orgueil.
In contrast, the CI-like chondrites Y-82162 and Y-980115 show lower mass loss (13.8–18.8 wt.%) and contain >50 % less H2O than the CI chondrites. The 3-μm feature is almost absent from spectra of Y-82162 and Y-980115 but the 11-μm feature is intense. The CI-like chondrites experienced thermal metamorphism at temperatures >500 °C that initially caused dehydration and dehydroxylation of phyllosilicates before partial recrystallization back into anhydrous silicates. The surfaces of many C-type asteroids were probably heated through impact metamorphism and/or solar radiation, so thermally altered carbonaceous chondrites are likely good analogues for samples that will be returned by the Hayabusa-2 and OSIRIS-REx missions
Comparison of transcriptome-derived simple sequence repeat (SSR) and single nucleotide polymorphism (SNP) markers for genetic fingerprinting, diversity evaluation, and establishment of relationships in eggplants
[EN] Simple sequence repeat (SSR) and single nucleotide polymorphism (SNP) markers are amongst the most common markers of choice for studies of diversity and relationships in horticultural species. We have used 11 SSR and 35 SNP markers derived from transcriptome sequencing projects to fingerprint 48 accessions of a collection of brinjal (Solanum melongena), gboma (S. macrocarpon) and scarlet (S. aethiopicum) eggplant complexes, which also include their respective wild relatives S. incanum, S. dasyphyllum and S. anguivi. All SSR and SNP markers were polymorphic and 34 and 36 different genetic fingerprints were obtained with SSRs and SNPs, respectively. When combining both markers all accessions but two had different genetic profiles. Although on average SSRs were more informative than SNPs, with a higher number of alleles, genotypes and polymorphic information content (PIC), and expected heterozygosity (He) values, SNPs have proved highly informative in our materials. Low observed heterozygosity (Ho) and high fixation index (f) values confirm the high degree of homozygosity of eggplants. Genetic identities within groups of each complex were higher than with groups of other complexes, although differences in the ranks of genetic identity values among groups were observed between SSR and SNP markers. For low and intermediate values of pair-wise SNP genetic distances, a moderate correlation between SSR and SNP genetic distances was observed (r(2) = 0.592), but for high SNP genetic distances the correlation was low (r(2) = 0.080). The differences among markers resulted in different phenogram topologies, with a different eggplant complex being basal (gboma eggplant for SSRs and brinjal eggplant for SNPs) to the two others. Overall the results reveal that both types of markers are complementary for eggplant fingerprinting and that interpretation of relationships among groups may be greatly affected by the type of marker used.This work has been funded by European Union's Horizon 2020 Research and Innovation Programme under Grant Agreement No 677379 (G2P-SOL project: Linking genetic resources, genomes and phenotypes of Solanaceous crops) and by Spanish Ministerio de Economia y Competitividad and Fondo Europeo de Desarrollo Regional (Grant AGL2015-64755-R from MINECO/FEDER). Pietro Gramazio is grateful to Universitat Politecnica de Valencia for a pre-doctoral contract (Programa FPI de la UPV-Subprograma 1/2013 call). Mariola Plazas is grateful to Spanish Ministerio de Economia, Industria y Competitividad for a post-doctoral grant within the Juan de la Cierva-Formacion programme (FJCI-2015-24835).Gramazio, P.; Prohens Tomás, J.; Borras, D.; Plazas Ávila, MDLO.; Herraiz García, FJ.; Vilanova Navarro, S. (2017). Comparison of transcriptome-derived simple sequence repeat (SSR) and single nucleotide polymorphism (SNP) markers for genetic fingerprinting, diversity evaluation, and establishment of relationships in eggplants. Euphytica. 213(264):1-18. https://doi.org/10.1007/s10681-017-2057-3S118213264Acquadro A, Barchi L, Gramazio P et al (2017) Coding SNPs analysis highlights genetic relationships and evolution pattern in eggplant complexes. PLoS ONE 12:e0180774. https://doi.org/10.1371/journal.pone.0180774Adeniji O, Kusolwa P, Reuben S (2013) Morphological descriptors and micro satellite diversity among scarlet eggplant groups. Afr Crop Sci J 21(1):37–49Aguoru C, Omoigui L, Olasan J (2015) Molecular characterization of Solanum species (Solanum aethiopicum complex; Solanum macrocarpon and Solanum anguivi) using multiplex RAPD primers. J Plant Stud 4:27–34. https://doi.org/10.5539/jps.v4n1p27Arumuganathan K, Earle E (1991) Nuclear DNA content of some important plant species. Plant Mol Biol Rep 9(3):208–218Ashrafi H, Hill T, Stoffel K et al (2012) De novo assembly of the pepper transcriptome (Capsicum annuum): a benchmark for in silico discovery of SNPs, SSRs and candidate genes. BMC Genom 13:1–15. https://doi.org/10.1186/1471-2164-13-571Augustinos AA, Petropoulos C, Karasoulou V et al (2016) Assessing diversity among traditional Greek and foreign eggplant cultivars using molecular markers and morphometrical descriptors. Span J Agric Res 14:e0710. https://doi.org/10.5424/sjar/2016144-9020Avise JC (2012) Molecular markers, natural history and evolution. Springer Science & Business Media, Berlin. https://doi.org/10.1007/978-1-4615-2381-9Blanca J, Cañizares J, Roig C et al (2011) Transcriptome characterization and high throughput SSRs and SNPs discovery in Cucurbita pepo (Cucurbitaceae). BMC Genom 12:104. https://doi.org/10.1186/1471-2164-12-104Botstein D, White RL, Skolnick M, Davis RW (1980) Construction of a genetic linkage map in man using restriction fragment length polymorphisms. Am J Hum Genet 32(3):314–331Bukenya Z, Carasco J (1994) Biosystematic study of Solanum macrocarpon—S. dasyphyllum complex in Uganda and relations with Solanum linnaeanum. East Afr Agric For J 59(3):187–204Castillo A, Budak H, Varshney RK et al (2008) Transferability and polymorphism of barley EST-SSR markers used for phylogenetic analysis in Hordeum chilense. BMC Plant Biol 8:97. https://doi.org/10.1186/1471-2229-8-97Choudhary S, Sethy NK, Shokeen B, Bhatia S (2009) Development of chickpea EST-SSR markers and analysis of allelic variation across related species. Theor Appl Genet 118:591–608. https://doi.org/10.1007/s00122-008-0923-zCoates BS, Sumerford DV, Miller NJ et al (2009) Comparative performance of single nucleotide polymorphism and microsatellite markers for population genetic analysis. J Hered 100:556–564. https://doi.org/10.1093/jhered/esp028D’Agostino N, Golas T, van de Geest H et al (2013) Genomic analysis of the native European Solanum species, S. dulcamara. BMC Genom 14:356. https://doi.org/10.1186/1471-2164-14-356Daunay MC, Hazra P (2012) Eggplant. In: Peter KV, Hazra P (eds) Handbook of Vegetables. Studium Press, Houston, pp 257–322Davey J, Hohenlohe P, Etter P et al (2011) Genome-wide genetic marker discovery and genotyping using next-generation sequencing. Nat Rev Genet 12:499–510. https://doi.org/10.1038/nrg3012De Barba M, Miquel C, Lobréaux S et al (2016) High-throughput microsatellite genotyping in ecology: improved accuracy, efficiency, standardization and success with low-quantity and degraded DNA. Mol Ecol Resour 17(3):492–507. https://doi.org/10.1111/1755-0998.12594Doyle J, Doyle J (1987) A rapid DNA isolation procedure for small quantities of fresh leaf tissue. Phytochem Bull 19:11–15Ellegren H (2004) Microsatellites: simple sequences with complex evolution. Nat Rev Genet 5:435–445. https://doi.org/10.1038/nrg1348Felsenstein, J (2007). PHYLIP (Phylogeny Inference Package) Version 3.67. Department of Genome Sciences, University of Washington, Seattle, WA, USAFernandez-Silva I, Whitney J, Wainwright B (2013) Microsatellites for next-generation ecologists: a post-sequencing bioinformatics pipeline. PLoS ONE 8(2):e55990Filippi CV, Aguirre N, Rivas JG et al (2015) Population structure and genetic diversity characterization of a sunflower association mapping population using SSR and SNP markers. BMC Plant Biol 15:52. https://doi.org/10.1186/s12870-014-0360-xFischer MC, Rellstab C, Leuzinger M et al (2017) Estimating genomic diversity and population differentiation—an empirical comparison of microsatellite and SNP variation in Arabidopsis halleri. BMC Genom 18:69. https://doi.org/10.1186/s12864-016-3459-7Furini A, Wunder J (2004) Analysis of eggplant (Solanum melongena)-related germplasm: morphological and AFLP data contribute to phylogenetic interpretations and germplasm utilization. Theor Appl Genet 108:197–208. https://doi.org/10.1007/s00122-003-1439-1Gadaleta A, Giancaspro A, Zacheo S et al (2011) Comparison of genomic and EST-derived SSR markers in phylogenetic analysis of wheat. Plant Genet Resour 9:243–246. https://doi.org/10.1017/S147926211100030XGe H, Liu Y, Jiang M et al (2013) Analysis of genetic diversity and structure of eggplant populations (Solanum melongena L.) in China using simple sequence repeat markers. Sci Hortic 162:71–75. https://doi.org/10.1016/j.scienta.2013.08.004Gonzaga ZJ (2015) Evaluation of SSR and SNP Markers for Molecular Breeding in Rice. Plant Breed Biotechnol 3:139–152. https://doi.org/10.9787/PBB.2015.3.2.139Goodwin S, McPherson J, McCombie W (2016) Coming of age: ten years of next-generation sequencing technologies. Nat Rev Genet 17(6):333–351Gramazio P, Blanca J, Ziarsolo P et al (2016) Transcriptome analysis and molecular marker discovery in Solanum incanum and S. aethiopicum, two close relatives of the common eggplant (Solanum melongena) with interest for breeding. BMC Genom 17:300. https://doi.org/10.1186/s12864-016-2631-4Grover A, Sharma PC (2014) Development and use of molecular markers: past and present. Crit Rev Biotechnol 8551:1–13. https://doi.org/10.3109/07388551.2014.959891Hamblin MT, Warburton ML, Buckler ES (2007) Empirical comparison of simple sequence repeats and single nucleotide polymorphisms in assessment of maize diversity and relatedness. PLoS ONE 2:e1367. https://doi.org/10.1371/journal.pone.0001367Hess JE, Matala AP (2011) Comparison of SNPs and microsatellites for fine-scale application of genetic stock identification of Chinook salmon in the Columbia River Basin Comparison of SNPs and microsatellites for fine-scale application of genetic stock identification of Chinook salmon in the Columbia River Basin. Mol Ecol Resour. https://doi.org/10.1111/j.1755-0998.2010.02958.xHighton R (1993) The relationship between the number of loci and the statistical support for the topology of UPGMA trees obtained from genetic distance data. Mol Phylogenet Evol 2:337–343Hirakawa H, Shirasawa K, Miyatake K, Nunome, T et al (2014) Draft genome sequence of eggplant (Solanum melongena L.): the representative solanum species indigenous to the old world. DNA Res 21:649–660. https://doi.org/10.1093/dnares/dsu027Hong CP, Piao ZY, Kang TW et al (2007) Genomic distribution of simple sequence repeats in Brassica rapa. Mol Cells 23:349–356.Hu J, Wang L, Li J (2011) Comparison of genomic SSR and EST-SSR markers for estimating genetic diversity in cucumber. Biol Plant 55:577–580. https://doi.org/10.1007/s10535-011-0129-0Isshiki S, Iwata N, Khan MMR (2008) ISSR variations in eggplant (Solanum melongena L.) and related Solanum species. Sci Hortic 117:186–190. https://doi.org/10.1016/j.scienta.2008.04.003Jones ES, Sullivan H, Bhattramakki D, Smith JSC (2007) A comparison of simple sequence repeat and single nucleotide polymorphism marker technologies for the genotypic analysis of maize (Zea mays L.). Theor Appl Genet 115:361–371. https://doi.org/10.1007/s00122-007-0570-9Kalia RK, Rai MK, Kalia S et al (2011) Microsatellite markers: an overview of the recent progress in plants. Euphytica 177:309–334Kashi Y, King DG (2006) Simple sequence repeats as advantageous mutators in evolution. Trends Genet 22:253–259. https://doi.org/10.1016/j.tig.2006.03.005Kaushik P, Prohens J, Vilanova S et al (2016) Phenotyping of eggplant wild relatives and interspecific hybrids with conventional and phenomics descriptors provides insight for their potential utilization in breeding. Front Plant Sci 7:677Kim C, Guo H, Kong W et al (2016) Application of genotyping by sequencing technology to a variety of crop breeding programs. Plant Sci 242:14–22Knapp S, Vorontsova MS, Prohens J (2013) Wild relatives of the eggplant (Solanum melongena L.: Solanaceae): new understanding of species names in a complex group. PLoS ONE 8:e57039Kruglyak S, Durrett RT, Schug MD, Aquadro CF (1998) Equilibrium distributions of microsatellite repeat length resulting from a balance between slippage events and point mutations. Proc Natl Acad Sci USA 95:10774–10778. https://doi.org/10.1073/pnas.95.18.10774Lester RN, Daunay MC (2003) Diversity of African vegetable Solanum species and its implications for a better understanding of plant domestication. Schriften zu Genetischen Ressourcen 22:137–152Lester RN, Niakan L (1986) Origin and domestication of the scarlet eggplant, Solanum aethiopicum, from S. anguivi in Africa. In: D’Arcy WG (ed) Solanaceae: biology and systematics. Columbia University Press, New York, pp 433–456Lester RN, Jaeger PML, Bleijendaal-Spierings BHM et al (1990) African eggplants-a review of collecting in West Africa. Plant Genet Resour Newsl 81:17–26Levin R, Myers N, Bohs L (2006) Phylogenetic relationships among the ‘spiny solanums’ (Solanum subgenus Leptostemonum, Solanaceae). Am J Bot 93(1):157–169Li WH, Gojobori T, Nei M (1981) Pseudogenes as a paradigm of neutral evolution. Nature 292:237–239Li YC, Korol AB, Fahima T et al (2002) Microsatellites: genomic distribution, putative functions and mutational mechanisms: a review. Mol Ecol 11:2453–2465Liu K, Muse S (2005) PowerMarker: an integrated analysis environment for genetic marker analysis. Bioinformatics 21:2128–2129Mantel N (1967) The detection of disease clustering and a generalized regression approach. Cancer Res 27:209–220. https://doi.org/10.1038/214637b0Martínez-Arias R, Calafell F, Mateu E et al (2001) Sequence variability of a human pseudogene. Genome Res 11:1071–1085. https://doi.org/10.1101/gr.167701Meyer RS, Karol KG, Little DP et al (2012) Phylogeographic relationships among Asian eggplants and new perspectives on eggplant domestication. Mol Phylogenet Evol 63:685–701. https://doi.org/10.1016/j.ympev.2012.02.006Muñoz-Falcón J, Prohens J, Vilanova S, Nuez F (2009) Diversity in commercial varieties and landraces of black eggplants and implications for broadening the breeders’ gene pool. Ann Appl Biol 154(3):453–465Nandha PS, Singh J (2014) Comparative assessment of genetic diversity between wild and cultivated barley using gSSR and EST-SSR markers. Plant Breed 133:28–35. https://doi.org/10.1111/pbr.12118Nei M (1972) Genetic distance between populations. Am Nat 106:283–292. https://doi.org/10.1086/282771Nunome T, Negoro S, Kono I et al (2009) Development of SSR markers derived from SSR-enriched genomic library of eggplant (Solanum melongena L.). Theor Appl Genet 119:1143–1153. https://doi.org/10.1007/s00122-009-1116-0Page R (2001) TreeView. Glasgow University, GlasgowPeakall P, Smouse R (2012) GenAlEx 6.5: genetic analysis in Excel. Population genetic software for teaching and research an update. Bioinformatics 28:2537–2539Pessarakli M, Dris R (2004) Pollination and breeding of eggplants. J Food Agric Environ 2:218–219Plazas M, Andújar I, Vilanova S et al (2014) Conventional and phenomics characterization provides insight into the diversity and relationships of hypervariable scarlet (Solanum aethiopicum L.) and gboma (S. macrocarpon L.) eggplant complexes. Front. Plant Sci 5:318Ranil R, Niran H, Plazas M et al (2015) Improving seed germination of the eggplant rootstock Solanum torvum by testing multiple factors using an orthogonal array design. Sci Hortic 193:174–181. https://doi.org/10.1016/j.scienta.2015.07.030Sakata Y, Lester RN (1997) Chloroplast DNA diversity in brinjal eggplant (Solanum melongena L.) and related species. Euphytica 97:295–301. https://doi.org/10.1023/A:1003000612441Sakata Y, Nishio T, Matthews PJ (1991) Chloroplast DNA analysis of eggplant (Solanum melongena) and related species for their taxonomic affinity. Euphytica 55:21–26Särkinen T, Bohs L, Olmstead RG, Knapp S (2013) A phylogenetic framework for evolutionary study of the nightshades (Solanaceae): a dated 1000-tip tree. BMC Evol Biol 13:214. https://doi.org/10.1186/1471-2148-13-214Scheben A, Batley J, Edwards D (2017) Genotyping-by-sequencing approaches to characterize crop genomes: choosing the right tool for the right application. Plant Biotechnol J 15:149–161Sneath P, Sokal R (1973) Numerical taxonomy. The principles and practice of numerical classification. W H Freeman Limited, San FranciscoStàgel A, Portis E, Toppino L et al (2008) Gene-based microsatellite development for mapping and phylogeny studies in eggplant. BMC Genom 9:357. https://doi.org/10.1186/1471-2164-9-357Sunseri F, Polignano GB, Alba V et al (2010) Genetic diversity and characterization of African eggplant germplasm collection. Afr J Plant Sci 4:231–241Syfert MM, Castañeda-Álvarez NP, Khoury CK et al (2016) Crop wild relatives of the brinjal eggplant (Solanum melongena): poorly represented in genebanks and many species at risk of extinction. Am J Bot 103:635–651. https://doi.org/10.3732/ajb.1500539Thiel T, Michalek W, Varshney R, Graner A (2003) Exploiting EST databases for the development and characterization of gene-derived SSR-markers in barley (Hordeum vulgare L.). Theor Appl Genet 106:411–422. https://doi.org/10.1007/s00122-002-1031-0Thomson MJ, Alfred J, Dangl J et al (2014) High-throughput SNP genotyping to accelerate crop improvement. Plant Breed Biotechnol 2:195–212. https://doi.org/10.9787/PBB.2014.2.3.195Thorvaldsdóttir H, Robinson JT, Mesirov JP (2013) Integrative genomics viewer (IGV): high-performance genomics data visualization and exploration. Brief Bioinform 14:178–192. https://doi.org/10.1093/bib/bbs017Tumbilen Y, Frary A, Daunay MC, Doganlar S (2011) Application of EST-SSRs to examine genetic diversity in eggplant and its close relatives. Turk J Biol 35:125–136. https://doi.org/10.3906/biy-0906-57van Inghelandt D, Melchinger AE, Lebreton C, Stich B (2010) Population structure and genetic diversity in a commercial maize breeding program assessed with SSR and SNP markers. Theor Appl Genet 120:1289–1299. https://doi.org/10.1007/s00122-009-1256-2Van Tassell CP, Smith TPL, Matukumalli LK et al (2008) SNP discovery and allele frequency estimation by deep sequencing of reduced representation libraries. Nat Methods 5:247–252. https://doi.org/10.1038/nmeth.1185Varshney R, Graner A, Sorrells M (2005) Genic microsatellite markers in plants: features and applications. Trends Biotechnol 23(1):48–55Varshney RK, Chabane K, Hendre PS et al (2007) Comparative assessment of EST-SSR, EST-SNP and AFLP markers for evaluation of genetic diversity and conservation of genetic resources using wild, cultivated and elite barleys. Plant Sci 173:638–649. https://doi.org/10.1016/j.plantsci.2007.08.010Vilanova S, Manzur JP, Prohens J (2012) Development and characterization of genomic simple sequence repeat markers in eggplant and their application to the study of diversity and relationships in a collection of different cultivar types and origins. Mol Breed 30:647–660. https://doi.org/10.1007/s11032-011-9650-2Vilanova S, Hurtado M, Cardona A (2014) Genetic diversity and relationships in local varieties of eggplant from different cultivar groups as assessed by genomic SSR markers. Not Bot Horti Agrobo Cluj-Napoca 42:59–65Vogel JP, Gu YQ, Twigg P et al (2006) EST sequencing and phylogenetic analysis of the model grass Brachypodium distachyon. Theor Appl Genet 113:186–195. https://doi.org/10.1007/s00122-006-0285-3Vorontsova MS, Stern S, Bohs L, Knapp S (2013) African spiny solanum (subgenus Leptostemonum, Solanaceae): a thorny phylogenetic tangle. Bot J Linn Soc 173:176–193. https://doi.org/10.1111/boj.12053Weese TL, Bohs L (2010) Eggplant origins: out of Africa, into the Orient. Taxon 59:49–56. https://doi.org/10.2307/27757050Wright S (1965) The interpretation of population structure by F-statistics with special regard to systems of mating. Evolution 19:395–420. https://doi.org/10.2307/2406450Xiao M, Zhang Y, Chen X et al (2013) Transcriptome analysis based on next-generation sequencing of non-model plants producing specialized metabolites of biotechnological interest. J Biotechnol 166:122–134. https://doi.org/10.1016/j.jbiotec.2013.04.004Yan J, Yang X, Shah T et al (2010) High-throughput SNP genotyping with the Goldengate assay in maize. Mol Breed 25:441–451. https://doi.org/10.1007/s11032-009-9343-2Yang X, Xu Y, Shah T et al (2011) Comparison of SSRs and SNPs in assessment of genetic relatedness in maize. Genetica 139:1045–1054. https://doi.org/10.1007/s10709-011-9606-9Yu J, Zhang Z, Zhu C et al (2009) Simulation appraisal of the adequacy of number of background markers for relationship estimation in association mapping. Plant Genome 2:63. https://doi.org/10.3835/plantgenome2008.09.0009Zhan L, Paterson I, Fraser B (2016) MEGASAT: automated inference of microsatellite genotypes from sequence data. Ecol Resour, Mol. https://doi.org/10.1111/1755-0998.1256
Saponosides stéroïdiques de l'aubergine (Solanum melongena L.) II. Variations des teneurs liées aux conditions de récolte, aux génotypes et à la quantité de graines des fruits
International audienc
Saponosides stéroïdiques de l'aubergine (Solanum melongena L.) I. Intérêt alimentaire, méthodologie d'analyse, localisation dans le fruit
International audienc
Presolar SiC abundances in primitive meteorites by NanoSIMS raster ion imaging of insoluble organic matter
Here we present results obtained with NanoSIMS raster ion imaging to determine the abundance of presolar SiC in the insoluble organic matter (IOM) extracted from a number of different classes of chondrites (both carbonaceous and ordinary). This builds on previous work [1] aimed at obtaining SiC abundances in primitive meteorites by
SIMS and comparing them with noble gas analyses.
Both IOM and presolar grains are found in similar
CI-like relative abundances in the matrices of the most
primitive chondrites [2, 3], indicating that a homogeneous
mixture of grains was incorporated in the various parent bodies [3]. Both are then subjected to thermal and hydrothermal processing after parent body formation [4]. However, there are significant variations in the matrix-normalized abundances of SiC grains estimated from noble gases carried by presolar grains, which suggest that the primitive chondrites did not form from a well-mixed reservoir of presolar grains. Variations in the source material were attributed to the destruction of presolar grains by heating in the solar nebula (temperatures that may have exceeded 700°C) and were linked to the volatile element fractionations in chondrites [5].
The CR chondrites have amongst the lowest matrix-normalized SiC abundances, and largest volatile element ractionations, reported in the carbonaceous chondrites [5]. However, they contain the most primitive IOM of any chondrite class [6-7], which has experienced peak temperatures of <300°C [8]. These lowtemperatures could not have affected the SiC grains or their noble gas concentrations, indicating that either the IOM escaped heating (implying that it is not presolar)or SiC was degassed/destroyed at low temperatures,
perhaps during parent body processing [3]. Thus, in order to resolve this contradiction, it is necessary to determine SiC abundances independently of noble gases. Ion imaging of SiC grains is a direct technique that has been shown to successfully identify presolar SiC grains amongst others
The potential for crop to wild hybridization in eggplant (Solanum melongena ; solanaceae) in southern India
Premise of the study: In India and elsewhere, transgenic Bt eggplant (Solanum melongena) has been developed to reduce insect herbivore damage, but published studies of the potential for pollen-mediated, crop-to-wild gene flow are scant. This information is useful for risk assessments as well as in situ conservation strategies for wild germplasm. Methods: In 2010-2014, we surveyed 23 populations of wild/weedy eggplant (Solanum insanum; known as wild brinjal), carried out hand-pollination experiments, and observed pollinators to assess the potential for crop-to-wild gene flow in southern India. Key results: Wild brinjal is a spiny, low-growing perennial commonly found in disturbed sites such as roadsides, wastelands, and sparsely vegetated areas near villages and agricultural fields. Fourteen of the 23 wild populations in our study occurred within 0.5 km of cultivated brinjal and at least nine flowered in synchrony with the crop. Hand crosses between wild and cultivated brinjal resulted in seed set and viable F-1 progeny. Wild brinjal flowers that were bagged to exclude pollinators did not set fruit, and fruit set from manual self-pollination was low. The exserted stigmas of wild brinjal are likely to promote outcrossing. The most effective pollinators appeared to be bees (Amegilla, Xylocopa, Nomia, and Heterotrigona spp.), which also were observed foraging for pollen on crop brinjal. Conclusion: Our findings suggest that hybridization is possible between cultivated and wild brinjal in southern India. Thus, as part of the risk assessment process, we assume that transgenes from the crop could spread to wild brinjal populations that occur nearby
Placentas from pregnancies conceived by IVF/ICSI have a reduced DNA methylation level at the H19 and MEST differentially methylated regions
Does IVF/ICSI have an effect on the epigenetic regulation of the human placenta? We found a reduced DNA methylation level at the H19 and MEST differentially methylated regions (DMRs), and an increased RNA expression of H19 in placentas from pregnancies conceived by IVF/ICSI when compared with placentas from spontaneous conception. Changes in fetal environment are associated with adverse health outcomes. The placenta is pivotal for intrauterine environment. Animal studies show that epigenetic regulation plays an important role in these environment-induced phenotypic effects. Also, the preimplantation embryo environment affects birthweight as well as the risk of chronic adult diseases. Epigenetic processes are sensitive to the environment, especially during the period around conception. Placental tissue was collected from 35 spontaneously conceived pregnancies and 35 IVF/ICSI (5 IVF, 30 ICSI) derived pregnancies. We quantitatively analysed the DNA methylation patterns of a number of consecutive CpGs in the core regions of DMRs and other regulatory regions of imprinted genes, since these are involved in placental and fetal growth and development. By using pyrosequencing, the DNA methylation at seven germline-derived primary DMRs was analysed quantitatively. Five of these are maternally methylated (MEST isoform and , PEG3, KCNQ1OT1 and SNRPN) and two are paternally methylated [H19 DMR and the intergenic region between DLK1 and MEG3 (IG-DMR)]. The post-fertilization-derived secondary DMRs, IGF2 (DMR0 and 2) and IG-DMR (CG7, also called MEG3 DMR), and the MEG3 promoter region were examined as well. In case of differential methylation between the two groups, the effect on gene expression was assessed by quantitative real-time PCR. Both the promoter region of MEST isoform and and the 6th CTCF binding site within the H19 DMR were significantly hypomethylated in the IVF/ICSI group. The phenomenon was consistently observed over all CpG sites analysed and not restricted to single CpG sites. The other primary and secondary DMRs were not affected. Expression of H19 was increased in the IVF/ICSI group, while that of IGF2 and MEST remained similar. In the IVF/ICSI group, mostly ICSI pregnancies were investigated. The ICSI technique or male subfertility could be a confounding factor. Therefore, our results are less generalizable to IVF pregnancies. The clinical effects of the observed placental hypomethylations on the developmental programming of the IVF/ICSI progeny, if any, are as yet unknown. Whether the hypomethylation is an adaptation of the placenta to maintain fetal supply and ameliorate the effects of environmental cues, or whether it is a deregulation leading to deranged developmental programming with or without increased vulnerability for disease, consistent with the developmental origins of health and disease hypothesis, needs further investigation. Partly funded by an unrestricted research grant by Organon BV (now MSD BV) without any role in study design, data collection and analysis, or preparation of the manuscript. No conflict of interests to declare. Dutch Trial Registry (NTR) number 1298
Bewertung von Solanum-Veredelungsunterlagen hinsichtlich ihrer Resistenz gegenüber Wurzelgallennematoden und Tobamoviren
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