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1.
Plant J ; 72(4): 636-51, 2012 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-22804913

RESUMEN

LTR retrotransposons and retroviruses are closely related. Although a viral envelope gene is found in some LTR retrotransposons and all retroviruses, only the latter show infectivity. The identification of Ty3-gypsy-like retrotransposons possessing putative envelope-like open reading frames blurred the taxonomical borders and led to the establishment of the Errantivirus, Metavirus and Chromovirus genera within the Metaviridae. Only a few plant Errantiviruses have been described, and their evolutionary history is not well understood. In this study, we investigated 27 retroelements of four abundant Elbe retrotransposon families belonging to the Errantiviruses in Beta vulgaris (sugar beet). Retroelements of the Elbe lineage integrated between 0.02 and 5.59 million years ago, and show family-specific variations in autonomy and degree of rearrangements: while Elbe3 members are highly fragmented, often truncated and present in a high number of solo LTRs, Elbe2 members are mainly autonomous. We observed extensive reshuffling of structural motifs across families, leading to the formation of new retrotransposon families. Elbe retrotransposons harbor a typical envelope-like gene, often encoding transmembrane domains. During the course of Elbe evolution, the additional open reading frames have been strongly modified or independently acquired. Taken together, the Elbe lineage serves as retrotransposon model reflecting the various stages in Errantivirus evolution, and allows a detailed analysis of retrotransposon family formation.


Asunto(s)
Beta vulgaris/genética , Evolución Molecular , Genoma de Planta , Virus de Plantas/genética , Recombinación Genética , Retroelementos , Secuencia de Aminoácidos , Beta vulgaris/virología , Cromosomas de las Plantas/genética , Biología Computacional/métodos , Secuencia Conservada , Variación Genética , Datos de Secuencia Molecular , Motivos de Nucleótidos , Sistemas de Lectura Abierta , Mapeo Físico de Cromosoma , Virus de Plantas/clasificación , Alineación de Secuencia , Especificidad de la Especie
2.
Theor Appl Genet ; 125(1): 185-96, 2012 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-22371142

RESUMEN

Potato variety discrimination based on morphological traits is laborious and influenced by the environment, while currently applied molecular markers are either expensive or time-consuming in development or application. SINEs, short interspersed nuclear elements, are retrotransposons with a high copy number in plant genomes representing a potential source for new markers. We developed a marker system for potato genotyping, designated inter-SINE amplified polymorphism (ISAP). Based on nine potato SINE families recently characterized (Wenke et al. in Plant Cell 23:3117-3128, 2011), we designed species-specific SINE primers. From the resulting 153 primer combinations, highly informative primer sets were selected for potato variety analysis regarding number of bands, quality of the banding pattern, and the degree of polymorphism. Fragments representing ISAPs can be separated by conventional agarose gel electrophoresis; however, automation with a capillary sequencer is feasible. Two selected SINE families, SolS-IIIa and SolS-IV, were shown to be highly but differently amplified in Solanaceae, Solaneae tribe, including wild and cultivated potatoes, tomato, and eggplant. Fluorescent in situ hybridization demonstrated the genome-wide distribution of SolS-IIIa and SolS-IV along potato chromosomes, which is the basis for genotype discrimination and differentiation of somaclonal variants by ISAP markers.


Asunto(s)
Técnicas de Genotipaje/métodos , Elementos de Nucleótido Esparcido Corto/genética , Solanum tuberosum/clasificación , Solanum tuberosum/genética , Cromosomas de las Plantas/genética , Análisis por Conglomerados , Electroforesis en Gel de Agar , Marcadores Genéticos , Genoma de Planta/genética , Genotipo , Hibridación Fluorescente in Situ , Mutación/genética , Reacción en Cadena de la Polimerasa , Polimorfismo Genético
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