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1.
Planta ; 249(4): 1157-1175, 2019 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-30603787

RESUMEN

MAIN CONCLUSION: Stable QTL for grain protein content co-migrating with nitrogen-related genes have been identified by the candidate genes and genome-wide association mapping approaches useful for marker-assisted selection. Grain protein content (GPC) is one of the most important quality traits in wheat, defining the nutritional and end-use properties and rheological characteristics. Over the years, a number of breeding programs have been developed aimed to improving GPC, most of them having been prevented by the negative correlation with grain yield. To overcome this issue, a collection of durum wheat germplasm was evaluated for both GPC and grain protein deviation (GPD) in seven field trials. Fourteen candidate genes involved in several processes related to nitrogen metabolism were precisely located on two high-density consensus maps of common and durum wheat, and six of them were found to be highly associated with both traits. The wheat collection was genotyped using the 90 K iSelect array, and 11 stable quantitative trait loci (QTL) for GPC were detected in at least three environments and the mean across environments by the genome-wide association mapping. Interestingly, seven QTL were co-migrating with N-related candidate genes. Four QTL were found to be significantly associated to increases of GPD, indicating that selecting for GPC could not affect final grain yield per spike. The combined approaches of candidate genes and genome-wide association mapping led to a better understanding of the genetic relationships between grain storage proteins and grain yield per spike, and provided useful information for marker-assisted selection programs.


Asunto(s)
Grano Comestible/química , Genes de Plantas/genética , Proteínas de Plantas/análisis , Triticum/genética , ADN de Plantas/genética , ADN de Plantas/aislamiento & purificación , Genes de Plantas/fisiología , Estudio de Asociación del Genoma Completo , Técnicas de Genotipaje , Polimorfismo de Nucleótido Simple/genética , Sitios de Carácter Cuantitativo/genética , Triticum/química , Triticum/metabolismo
2.
Phys Rev Lett ; 111(8): 087204, 2013 Aug 23.
Artículo en Inglés | MEDLINE | ID: mdl-24010471

RESUMEN

Possible ferromagnetism induced in otherwise nonmagnetic materials has been motivating intense research in complex oxide heterostructures. Here we show that a confined magnetism is realized at the interface between SrTiO3 and two insulating polar oxides, BiMnO3 and LaAlO3. By using polarization dependent x-ray absorption spectroscopy, we find that in both cases the magnetism can be stabilized by a negative exchange interaction between the electrons transferred to the interface and local magnetic moments. These local magnetic moments are associated with magnetic Ti3+ ions at the interface itself for LaAlO3/SrTiO3 and to Mn3+ ions in the overlayer for BiMnO3/SrTiO3. In LaAlO3/SrTiO3 the induced magnetism is quenched by annealing in oxygen, suggesting a decisive role of oxygen vacancies in this phenomenon.

3.
Genome ; 55(6): 417-27, 2012 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-22624876

RESUMEN

The aims of the present study were to provide deletion maps for wheat ( Triticum aestivum L.) chromosomes 5A and 5B and a detailed genetic map of chromosome 5A enriched with popular microsatellite markers, which could be compared with other existing maps and useful for mapping major genes and quantitative traits loci (QTL). Physical mapping of 165 gSSR and EST-SSR markers was conducted by amplifying each primer pair on Chinese Spring, aneuploid lines, and deletion lines for the homoeologous group 5 chromosomes. A recombinant inbred line (RIL) mapping population that is recombinant for only chromosome 5A was obtained by crossing the wheat cultivar Chinese Spring and the disomic substitution line Chinese Spring-5A dicoccoides and was used to develop a genetic linkage map of chromosome 5A. A total of 67 markers were found polymorphic between the parental lines and were mapped in the RIL population. Sixty-three loci and the Q gene were clustered in three linkage groups ordered at a minimum LOD score of 5, while four loci remained unlinked. The whole genetic 5A chromosome map covered 420.2 cM, distributed among three linkage groups of 189.3, 35.4, and 195.5 cM. The EST sequences located on chromosomes 5A and 5B were used for comparative analysis against Brachypodium distachyon (L.) P. Beauv. and rice ( Oryza sativa L.) genomes to resolve orthologous relationships among the genomes of wheat and the two model species.


Asunto(s)
Secuencia de Bases , Cromosomas de las Plantas/genética , Genes de Plantas , Genoma de Planta , Eliminación de Secuencia , Triticum/genética , Brachypodium/genética , Mapeo Cromosómico , Cartilla de ADN , Etiquetas de Secuencia Expresada , Ligamiento Genético , Repeticiones de Microsatélite , Familia de Multigenes , Oryza/genética , Sitios de Carácter Cuantitativo
4.
BMC Infect Dis ; 10: 87, 2010 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-20359364

RESUMEN

BACKGROUND: Co-infection with Plasmodium falciparum malaria and Parvovirus B19 in adults is an extremely rare occurrence and, apparently, only one case has been previously reported. Herein we describe a case of acute co-infection with severe anemia and renal failure. CASE PRESENTATION: The patient was a 34-year-old African man presenting myalgia, fatigue, headache, anemia and hepatosplenomegaly. A thin peripheral smear showed Plasmodium falciparum trophozoites and the patient was treated with oral mefloquine. After an initial amelioration, fever, fatigue and myalgia reappeared, the anemia worsened and there was evidence of acute renal failure. No malarial parasites were found with a blood smear. A bone marrow aspiration showed marked erythroid hypoplasia. Parvovirus B19-specific IgM and IgG and viremia were positive. The patient was treated with steroids and blood cell transfusions. After ten days, anemia and renal failure progressively decreased. When last seen, the patient was asymptomatic and the blood values were within the normal range. CONCLUSIONS: The diagnosis of Parvovirus B19 acute infection should be considered in any case of persistent severe anemia and/or renal failure, even in clinical conditions that are well-known causes of anemia and renal failure, such as malaria.


Asunto(s)
Anemia/etiología , Malaria Falciparum/complicaciones , Infecciones por Parvoviridae/complicaciones , Parvovirus B19 Humano/aislamiento & purificación , Plasmodium falciparum/aislamiento & purificación , Insuficiencia Renal/etiología , Adulto , Antiinflamatorios/uso terapéutico , Anticuerpos Antivirales/sangre , Antimaláricos/uso terapéutico , Transfusión Sanguínea , Humanos , Inmunoglobulina G/sangre , Inmunoglobulina M/sangre , Malaria Falciparum/tratamiento farmacológico , Malaria Falciparum/parasitología , Malaria Falciparum/patología , Masculino , Mefloquina/uso terapéutico , Infecciones por Parvoviridae/patología , Infecciones por Parvoviridae/virología , Esteroides/uso terapéutico , Viremia
5.
Theor Appl Genet ; 118(5): 1015-25, 2009 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-19183861

RESUMEN

The availability of genetic maps and phenotypic data of segregating populations allows to localize and map agronomically important genes, and to identify closely associated molecular markers to be used in marker-assisted selection and positional cloning. The objective of the present work was to develop a durum wheat intervarietal genetic and physical map based on genomic microsatellite or genomic simple sequence repeats (gSSR) markers and expressed sequence tag (EST)-derived microsatellite (EST-SSR) markers. A set of 122 new EST-SSR loci amplified by 100 primer pairs was genetically mapped on the wheat A and B genome chromosomes. The whole map also comprises 149 gSSR markers amplified by 120 primer pairs used as anchor chromosome loci, two morphological markers (Black colour, Bla1, and spike glaucousness, Ws) and two seed storage protein loci (Gli-A2 and Gli-B2). The majority of SSR markers tested (182) was chromosome-specific. Out of 275 loci 241 loci assembled in 25 linkage groups assigned to the chromosomes of the A and B genome and 34 remained unlinked. A higher percentage of markers (54.4%), localized on the B genome chromosomes, in comparison to 45.6% distributed on the A genome. The whole map covered 1,605 cM. The B genome accounted for 852.2 cM of genetic distance; the A genome basic map spanned 753.1 cM with a minimum length of 46.6 cM for chromosome 5A and a maximum of 156.2 cM for chromosome 3A and an average value of 114.5 cM. The primer sets that amplified two or more loci mapped to homoeologous as well as to non-homoeologous sites. Out of 241 genetically mapped loci 213 (88.4%) were physically mapped by using the nulli-tetrasomic, ditelosomic and a stock of 58 deletion lines dividing the A and B genome chromosomes in 94 bins. No discrepancies concerning marker order were observed but the cytogenetic maps revealed in some cases small genetic distance covered large physical regions. Putative function for mapped SSRs were assigned by searching against GenBank nonredundant database using TBLASTX algorithms.


Asunto(s)
Mapeo Cromosómico , Cromosomas de las Plantas , Etiquetas de Secuencia Expresada , Genoma de Planta , Repeticiones de Minisatélite/genética , Triticum/genética , Marcadores Genéticos , Datos de Secuencia Molecular , Polimorfismo Genético
6.
Surg Neurol ; 20(3): 254-7, 1983 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-6879428

RESUMEN

Two cases of femoral neuropathy caused by iliacus hematoma occurring during anticoagulant therapy are described. The pathogenesis and the clinical picture of this particular pathology are discussed and the necessity of early surgical decompression is emphasized.


Asunto(s)
Nervio Femoral , Hematoma/complicaciones , Ilion , Síndromes de Compresión Nerviosa/etiología , Anticoagulantes/efectos adversos , Enfermedades Óseas/complicaciones , Enfermedades Óseas/diagnóstico por imagen , Enfermedades Óseas/etiología , Femenino , Hematoma/diagnóstico por imagen , Hematoma/etiología , Humanos , Masculino , Persona de Mediana Edad , Tomografía Computarizada por Rayos X
7.
Minerva Med ; 75(20): 1199-204, 1984 May 12.
Artículo en Italiano | MEDLINE | ID: mdl-6728270

RESUMEN

103 patient suffering from thyroid solitary nodule have been examined with gray-scale ultrasonography. 79 patients have been histologically confirmed. Research has been done with multi-transducer computerized water-bath equipment ( OCTOSON ). The results are discussed and a classification of the thyroid solitary nodule in four groups is proposed, according to the echographic patterns.


Asunto(s)
Neoplasias de la Tiroides/diagnóstico , Ultrasonografía , Adenoma/diagnóstico , Carcinoma Papilar/diagnóstico , Quistes/diagnóstico , Humanos , Enfermedades de la Tiroides/diagnóstico , Tiroiditis/diagnóstico
10.
Theor Appl Genet ; 117(1): 135-42, 2008 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-18392800

RESUMEN

Powdery mildew, caused by Blumeria graminis f.sp. tritici, is one of the most important wheat diseases in many regions of the world. Triticum turgidum var. dicoccoides (2n=4x=AABB), the progenitor of cultivated wheats, shows particular promises as a donor of useful genetic variation for several traits, including disease resistances. The wild emmer accession MG29896, resistant to powdery mildew, was backcrossed to the susceptible durum wheat cultivar Latino, and a set of backcross inbred lines (BC(5)F(5)) was produced. Genetic analysis of F(3) populations from two resistant introgression lines (5BIL-29 x Latino and 5BIL-42 x Latino) indicated that the powdery mildew resistance is controlled by a single dominant gene. Molecular markers and the bulked segregant analysis were used to characterize and map the powdery mildew resistance. Five AFLP markers (XP43M32((250)), XP46M31((410)), XP41M37((100)), XP41M39((250)), XP39M32((120))), three genomic SSR markers (Xcfd07, Xwmc75, Xgwm408) and one EST-derived SSR marker (BJ261635) were found to be linked to the resistance gene in 5BIL-29 and only the BJ261635 marker in 5BIL-42. By means of Chinese Spring nullisomic-tetrasomic, ditelosomic and deletion lines, the polymorphic markers and the resistance gene were assigned to chromosome bin 5BL6-0.29-0.76. These results indicated that the two lines had the same resistance gene and that the introgressed dicoccoides chromosome segment was longer (35.5 cM) in 5BIL-29 than that introgressed in 5BIL-42 (less than 1.5 cM). As no powdery mildew resistance gene has been reported on chromosome arm 5BL, the novel resistance gene derived from var. dicoccoides was designated Pm36. The 244 bp allele of BJ261635 in 5BIL-42 can be used for marker-assisted selection during the wheat resistance breeding process for facilitating gene pyramiding.


Asunto(s)
Ascomicetos , Mapeo Cromosómico , ADN de Plantas/genética , Genes de Plantas , Enfermedades de las Plantas/genética , Triticum/genética , Análisis del Polimorfismo de Longitud de Fragmentos Amplificados , Cromosomas de las Plantas/genética , Cruzamientos Genéticos , Etiquetas de Secuencia Expresada , Ligamiento Genético , Marcadores Genéticos , Variación Genética , Repeticiones de Minisatélite , Enfermedades de las Plantas/microbiología , Triticum/microbiología
11.
Theor Appl Genet ; 112(7): 1195-204, 2006 May.
Artículo en Inglés | MEDLINE | ID: mdl-16453131

RESUMEN

Grain protein content (GPC) of durum wheat (Triticum turgidum L. var. durum) is an important trait for the nutritional value of grain and for influencing the technological property of flour. Protein content is a quantitative trait negatively correlated with grain yield, thus increase in protein quantity usually results in yield reduction. This study was initiated to introgress alleles for high GPC from var. dicoccoides into durum wheat germplasm by the backcross inbred line (BIL) method and to identify molecular markers linked to high GPC alleles not associated with depressing effects on yield. The backcross line 3BIL-85 with high GPC and similar grain yield to the recurrent parent was backcrossed to Latino, and the generations F2, F3 and F4 were evaluated for GPC and yield per spike (GYS) in three field trials. Three QTLs with major effects on GPC were detected on chromosome arms 2AS, 6AS and 7BL, identified by the markers Xcfa2164, XP39M37 (250) and Xgwm577, respectively. Multiple regression analysis indicated that the three QTLs explained all the genetic variances of the trait. The high GPC parental line 3BIL-85 was not significantly different from the recurrent parent Latino for GYS, but the phenotypic correlation coefficient between GPC and GYS had negative values (from -0.02 to -0.28) in each trial, although it was statistically significant only in the F3 progeny trial. No co-located QTL for GYS was detected, excluding the hypothesis that the putative QTLs for GPC were indirect QTLs for low grain yield. The negative protein-yield response could be due to: (a) co-location of grain yield per spike QTLs with reduced phenotypic effects not detectable by the experimental design or statistical procedures, or to (b) opposite pleiotropic gene effects due to the major bio-energetic requirements for synthesis of protein then carbohydrates. Mapping loci by BILs should enable the production of near-isogenic lines in which the individual effects of each QTL can be examined in detail without confounding variations due to other putative QTLs.


Asunto(s)
Grano Comestible/química , Proteínas de Plantas/metabolismo , Sitios de Carácter Cuantitativo , Triticum/genética , Alelos , Mapeo Cromosómico , Cromosomas de las Plantas , Cruzamientos Genéticos , Marcadores Genéticos , Triticum/metabolismo
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