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1.
Yi Chuan ; 35(9): 1117-24, 2013 Sep.
Artículo en Chino | MEDLINE | ID: mdl-24400486

RESUMEN

LTR-Retrotransposons are the major DNA components in plant genomes. They usually contain gag and pol, two genes necessary for transpositinal process. Our previous study on soybean genome annotation identified a SARE LTR-Retrotransposon family, which carries the third gene, Orf1. Using a bioinformatics approach, we here reported that 7 out of 33 sequenced genomes have some LTR-Retrotransposons with an extra Orf1 gene/gene fragment (approximately 1-2 kb) in the region between 5' LTR and gag gene, including Eucalyptus grandis, Populus trichocarpa, Gossypium raimondii, Glycine max, Lotus japonica, Linum usitatissimum, and Medicago truncatula. The majority of these elements were inserted into the genomes they reside within the last 3 million years, but their structures, frequencies, intensity, and activity in different host genomes are quite different. Phylogenetic analysis indicated that these unusual elements were clustered in a eudicot branch, suggesting that they may be generated in the evolution of some eudicot species. The relative conservation, transcriptional activity, and the presence of multiple potential conserved motifs suggest that Orf1 gene may still be functional.


Asunto(s)
Genoma de Planta , Proteínas de Plantas/genética , Plantas/genética , Retroelementos , Secuencia de Aminoácidos , Datos de Secuencia Molecular , Filogenia , Proteínas de Plantas/química , Plantas/química , Plantas/clasificación , Alineación de Secuencia
2.
J Antibiot (Tokyo) ; 59(10): 669-72, 2006 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-17191684

RESUMEN

One lactone marasmane sesquiterpene named 8a,13-dihydroxy-marasm-5-oic acid gamma-lactone (1) and one unsaturated marasmane sesquiterpene named 13-hydroxy-marasm-7(8)-en-5-methoxy gamma-acetal (2) together with a known compound: 7alpha, 8alpha, 13-trihydroxy-marasm-5-oic acid gamma-lactone (3) were isolated from the fruiting bodies of Russula foetens. Their structures were established on the basis of spectral methods (MS, IR, ID and 2D NMR experiments).


Asunto(s)
Basidiomycota/química , Sesquiterpenos/química , Sesquiterpenos/aislamiento & purificación , Espectroscopía de Resonancia Magnética , Estructura Molecular , Triterpenos/química , Triterpenos/aislamiento & purificación
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