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1.
Genetics ; 203(2): 817-29, 2016 06.
Artículo en Inglés | MEDLINE | ID: mdl-27075727

RESUMEN

Angiosperm reproduction requires the integrated development of multiple tissues with different genotypes. To achieve successful fertilization, the haploid female gametophytes and diploid ovary must coordinate their development, after which the male gametes must navigate through the maternal sporophytic tissues to reach the female gametes. After fertilization, seed development requires coordinated development of the maternal diploid integuments, the triploid endosperm, and the diploid zygote. Transcription and signaling factors contribute to communication between these tissues, and roles for epigenetic regulation have been described for some of these processes. Here we identify a broad role for CHD3 chromatin remodelers in Arabidopsis thaliana reproductive development. Plants lacking the CHD3 remodeler, PICKLE, exhibit various reproductive defects including abnormal development of the integuments, female gametophyte, and pollen tube, as well as delayed progression of ovule and embryo development. Genetic analyses demonstrate that these phenotypes result from loss of PICKLE in the maternal sporophyte. The paralogous gene PICKLE RELATED 2 is preferentially expressed in the endosperm and acts antagonistically with respect to PICKLE in the seed: loss of PICKLE RELATED 2 suppresses the large seed phenotype of pickle seeds. Surprisingly, the alteration of seed size in pickle plants is sufficient to determine the expression of embryonic traits in the seedling primary root. These findings establish an important role for CHD3 remodelers in plant reproduction and highlight how the epigenetic status of one tissue can impact the development of genetically distinct tissues.


Asunto(s)
Proteínas de Arabidopsis/genética , Arabidopsis/genética , ADN Helicasas/genética , Células Germinativas de las Plantas/metabolismo , Arabidopsis/crecimiento & desarrollo , Proteínas de Arabidopsis/metabolismo , ADN Helicasas/metabolismo , Endospermo/crecimiento & desarrollo , Endospermo/metabolismo , Epigénesis Genética , Células Germinativas de las Plantas/crecimiento & desarrollo
2.
Development ; 142(3): 454-64, 2015 Feb 01.
Artículo en Inglés | MEDLINE | ID: mdl-25564655

RESUMEN

Aintegumenta-like (AIL) transcription factors are key regulators of cell proliferation and meristem identity. Although AIL functions have been well described, the direct signalling components of this pathway are largely unknown. We show that baby boom (BBM) and other AIL proteins physically interact with multiple members of the L1-expressed homeodomain glabrous (HDG) transcription factor family, including HDG1, HDG11 and HDG12. Overexpression of HDG1, HDG11 and HDG12 restricts growth due to root and shoot meristem arrest, which is associated with reduced expression of genes involved in meristem development and cell proliferation pathways, whereas downregulation of multiple HDG genes promotes cell overproliferation. These results suggest a role for HDG proteins in promoting cell differentiation. We also reveal a transcriptional network in which BBM and HDG1 regulate several common target genes, and where BBM/AIL and HDG regulate the expression of each other. Taken together, these results suggest opposite roles for AIL and HDG proteins, with AILs promoting cell proliferation and HDGs stimulating cell differentiation, and that these functions are mediated at both the protein-protein interaction and transcriptional level.


Asunto(s)
Proteínas de Arabidopsis/metabolismo , Arabidopsis/fisiología , Diferenciación Celular/fisiología , Proliferación Celular/fisiología , Regulación de la Expresión Génica de las Plantas/fisiología , Transducción de Señal/fisiología , Factores de Transcripción/metabolismo , Arabidopsis/metabolismo , Proteínas de Arabidopsis/genética , Inmunoprecipitación de Cromatina , Microscopía por Crioelectrón , Cartilla de ADN/genética , Citometría de Flujo , Transferencia Resonante de Energía de Fluorescencia , Regulación de la Expresión Génica de las Plantas/genética , Vectores Genéticos/genética , Análisis por Micromatrices , Microscopía Confocal , Familia de Multigenes/genética , Reacción en Cadena en Tiempo Real de la Polimerasa , Transducción de Señal/genética , Factores de Transcripción/genética
3.
Appl Microbiol Biotechnol ; 93(3): 1249-56, 2012 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-21842153

RESUMEN

Cry3 class toxins are used extensively for biological control of coleopteran larvae. We previously identified a peptide (PCx) from a phage display library that specifically binds Cx-cellulase from the midgut of Anoplophora glabripennis Motschulsky (Asian longhorn beetle) larvae. Here, we added a DNA fragment that encodes the peptide onto either end of the cry3Aa gene and tested the expressed PCx-Cry3Aa and Cry3Aa-PCx proteins for insecticidal activity in the longhorned beetle. An insect bioassay revealed that, compared with native Cry3Aa, the two modified Cry3Aa proteins had significantly higher lethality, with PCx-Cry3Aa exhibiting a mortality rate almost three times that of Cry3Aa. We also proposed that the increased lethality in larvae fed with PCx-Cry3Aa or Cry3Aa-PCx would be attributable to the binding of the toxin with Cx-cellulase, thereby increasing toxin retention in the midgut. The significantly enhanced insecticidal activity of Cry3Aa fused with the Cx-cellulase binding peptide provides a new strategy for increasing toxin efficacy against the longhorned beetle. These uniquely modified Cry3Aa proteins have potential use for pest control.


Asunto(s)
Celulasa/metabolismo , Escarabajos/efectos de los fármacos , Péptidos/metabolismo , Péptidos/farmacología , Control Biológico de Vectores , Proteínas Recombinantes de Fusión/farmacología , Animales , Bacillus thuringiensis/genética , Bacillus thuringiensis/metabolismo , Toxinas de Bacillus thuringiensis , Proteínas Bacterianas/genética , Proteínas Bacterianas/metabolismo , Proteínas Bacterianas/farmacología , Escarabajos/crecimiento & desarrollo , Sistema Digestivo/metabolismo , Endotoxinas/genética , Endotoxinas/metabolismo , Endotoxinas/farmacología , Proteínas Hemolisinas/genética , Proteínas Hemolisinas/metabolismo , Proteínas Hemolisinas/farmacología , Larva/efectos de los fármacos , Larva/crecimiento & desarrollo , Péptidos/genética , Control Biológico de Vectores/métodos , Proteínas Recombinantes de Fusión/genética , Proteínas Recombinantes de Fusión/metabolismo
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