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1.
Theor Appl Genet ; 115(4): 489-99, 2007 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-17619853

RESUMEN

Finger millet is an allotetraploid (2n = 4x = 36) grass that belongs to the Chloridoideae subfamily. A comparative analysis has been carried out to determine the relationship of the finger millet genome with that of rice. Six of the nine finger millet homoeologous groups corresponded to a single rice chromosome each. Each of the remaining three finger millet groups were orthologous to two rice chromosomes, and in all the three cases one rice chromosome was inserted into the centromeric region of a second rice chromosome to give the finger millet chromosomal configuration. All observed rearrangements were, among the grasses, unique to finger millet and, possibly, the Chloridoideae subfamily. Gene orders between rice and finger millet were highly conserved, with rearrangements being limited largely to single marker transpositions and small putative inversions encompassing at most three markers. Only some 10% of markers mapped to non-syntenic positions in rice and finger millet and the majority of these were located in the distal 14% of chromosome arms, supporting a possible correlation between recombination and sequence evolution as has previously been observed in wheat. A comparison of the organization of finger millet, Panicoideae and Pooideae genomes relative to rice allowed us to infer putative ancestral chromosome configurations in the grasses.


Asunto(s)
Eleusine/genética , Oryza/genética , Evolución Biológica , Mapeo Cromosómico , Cromosomas de las Plantas/genética , Duplicación de Gen , Ligamiento Genético , Marcadores Genéticos , Genoma de Planta , Poliploidía , Especificidad de la Especie
2.
Theor Appl Genet ; 114(2): 321-32, 2007 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-17103137

RESUMEN

Restriction fragment length polymorphism (RFLP), amplified fragment length polymorphism (AFLP), expressed-sequenced tag (EST), and simple sequence repeat (SSR) markers were used to generate a genetic map of the tetraploid finger millet (Eleusine coracana subsp. coracana) genome (2n = 4x = 36). Because levels of variation in finger millet are low, the map was generated in an inter-subspecific F(2) population from a cross between E. coracana subsp. coracana cv. Okhale-1 and its wild progenitor E. coracana subsp. africana acc. MD-20. Duplicated loci were used to identify homoeologous groups. Assignment of linkage groups to the A and B genome was done by comparing the hybridization patterns of probes in Okhale-1, MD-20, and Eleusine indica acc. MD-36. E. indica is the A genome donor to E. coracana. The maps span 721 cM on the A genome and 787 cM on the B genome and cover all 18 finger millet chromosomes, at least partially. To facilitate the use of marker-assisted selection in finger millet, a first set of 82 SSR markers was developed. The SSRs were identified in small-insert genomic libraries generated using methylation-sensitive restriction enzymes. Thirty-one of the SSRs were mapped. Application of the maps and markers in hybridization-based breeding programs will expedite the improvement of finger millet.


Asunto(s)
Mapeo Cromosómico , Eleusine/genética , Variación Genética
3.
Genetics ; 169(3): 1659-72, 2005 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-15654107

RESUMEN

Grass species differ in many aspects of inflorescence architecture, but in most cases the genetic basis of the morphological difference is unknown. To investigate the genes underlying the morphology in one such instance, we undertook a developmental and QTL analysis of inflorescence differences between the cereal grain foxtail millet and its presumed progenitor green millet. Inflorescence differences between these two species are the result of changes in primary branch number and density, spikelet number, and bristle (sterile branchlet) number; these differences also account for inflorescence variation within the clade of 300+ species that share the presence of bristles in the inflorescence. Fourteen replicated QTL were detected for the four inflorescence traits, and these are suggested to represent genes that control differences between the species. Comparative mapping using common markers from rice and maize allowed a number of candidate genes from maize to be localized to QTL regions in the millet genome. Searches of regions of the sequenced rice genome orthologous to QTL regions on foxtail millet identified a number of transcription factors and hormone pathway genes that may be involved in control of inflorescence branching.


Asunto(s)
Flores/genética , Variación Genética , Sitios de Carácter Cuantitativo , Setaria (Planta)/genética , Mapeo Cromosómico , Cromosomas de las Plantas , Flores/ultraestructura , Genes Dominantes , Marcadores Genéticos , Fenotipo , Polimorfismo de Longitud del Fragmento de Restricción , Setaria (Planta)/ultraestructura , Zea mays/genética
4.
Proc Natl Acad Sci U S A ; 101(24): 9045-50, 2004 Jun 15.
Artículo en Inglés | MEDLINE | ID: mdl-15184666

RESUMEN

Reduction in vegetative branching is commonplace when crops are domesticated from their wild progenitors. We have identified genetic loci responsible for these changes in foxtail millet (Setaria italica), a crop closely related to maize but whose genetics are little known. Quantitative trait locus (QTL) analysis and comparative genomics reveal that basal branching (tillering) and axillary branching are partially controlled by separate loci, and that the orthologue of teosinte branched1, the major gene controlling branching phenotype in maize, has only a minor and variable effect. We identify other candidate genes for control of branching, including a number of hormone biosynthesis pathway genes. These results suggest that similar phenotypic effects may not be produced by orthologous loci, even in closely related species, and that results from well characterized model systems such as maize must be reviewed critically before being applied to other species.


Asunto(s)
Setaria (Planta)/crecimiento & desarrollo , Setaria (Planta)/genética , Análisis de Varianza , Mapeo Cromosómico , Genoma de Planta , Funciones de Verosimilitud , Fenotipo , Hojas de la Planta/fisiología , Fenómenos Fisiológicos de las Plantas , Sitios de Carácter Cuantitativo/genética
5.
Proc Natl Acad Sci U S A ; 99(15): 10203-8, 2002 Jul 23.
Artículo en Inglés | MEDLINE | ID: mdl-12119408

RESUMEN

The maize (Zea mays) Viviparous 1 (Vp1) transcription factor has been shown previously to be a major regulator of seed development, simultaneously activating embryo maturation and repressing germination. Hexaploid bread wheat (Triticum aestivum) caryopses are characterized by relatively weak embryo dormancy and are susceptible to preharvest sprouting (PHS), a phenomenon that is phenotypically similar to the maize vp1 mutation. Analysis of Vp-1 transcript structure in wheat embryos during grain development showed that each homeologue produces cytoplasmic mRNAs of different sizes. The majority of transcripts are spliced incorrectly, contain insertions of intron sequences or deletions of coding region, and do not have the capacity to encode full-length proteins. Several VP-1-related lower molecular weight protein species were present in wheat embryo nuclei. Embryos of a closely related tetraploid species (Triticum turgidum) and ancestral diploids also contained misspliced Vp-1 transcripts that were structurally similar or identical to those found in modern hexaploid wheat, which suggests that compromised structure and expression of Vp-1 transcripts in modern wheat are inherited from ancestral species. Developing embryos from transgenic wheat grains expressing the Avena fatua Vp1 gene showed enhanced responsiveness to applied abscisic acid compared with the control. In addition, ripening ears of transgenic plants were less susceptible to PHS. Our results suggest that missplicing of wheat Vp-1 genes contributes to susceptibility to PHS in modern hexaploid wheat varieties and identifies a possible route to increase resistance to this environmentally triggered disorder.


Asunto(s)
Empalme Alternativo , Proteínas de Unión al ADN/genética , Factores de Transcripción/genética , Transcripción Genética , Triticum/genética , Secuencia de Bases , Cartilla de ADN , Datos de Secuencia Molecular , Filogenia , Proteínas de Plantas/genética , Plantas Modificadas Genéticamente , ARN de Planta/genética , ARN de Planta/aislamiento & purificación , Semillas/fisiología , Transactivadores , Triticum/clasificación , Triticum/crecimiento & desarrollo
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