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1.
BMC Genomics ; 20(1): 346, 2019 05 08.
Artículo en Inglés | MEDLINE | ID: mdl-31068144

RESUMEN

Following the publication of this article [1], the authors noted the following errors.

2.
BMC Genomics ; 19(1): 881, 2018 Dec 06.
Artículo en Inglés | MEDLINE | ID: mdl-30522435

RESUMEN

BACKGROUND: The eukaryotic unicellular protist Plasmodiophora brassicae is an endocellular parasite of cruciferous plants. In host cortical cells, this protist develops a unicellular structure that is termed the plasmodium. The plasmodium is actually a multinucleated cell, which subsequently splits and forms resting spores. The mechanism for the growth of this endocellular parasite in host cell is unclear. RESULTS: Here, combining de novo genome sequence and transcriptome analysis of strain ZJ-1, we identified top five significant enriched KEGG pathways of differentially expressed genes (DEGs), namely translation, cell growth and death, cell communication, cell motility and cancers. We detected 171 proto-oncogenes from the genome of P. brassicae that were implicated in cancer-related pathways, of which 46 were differential expression genes. Three predicted proto-oncogenes (Pb-Raf1, Pb-Raf2, and Pb-MYB), which showed homology to the human proto-oncogenes Raf and MYB, were specifically activated during the plasmodial growth in host cortical cells, demonstrating their involvement in the multinucleate development stage of the unicellular protist organism. Gene networks involved in the tumorigenic-related signaling transduction pathways and the activation of 12 core genes were identified. Inhibition of phosphoinositol-3-kinase relieved the clubroot symptom and significantly suppressed the development process of plasmodia. CONCLUSIONS: Proto-oncogene-related regulatory mechanisms play an important role in the plasmodial growth of P. brassicae.


Asunto(s)
Genoma de Protozoos , Plasmodiophorida/genética , Proto-Oncogenes/genética , Secuencia de Aminoácidos , Brassica napus/metabolismo , Brassica napus/parasitología , Perfilación de la Expresión Génica , Genes myb/genética , Humanos , Imidazoles/farmacología , Imidazoles/uso terapéutico , Oxazepinas/farmacología , Oxazepinas/uso terapéutico , Enfermedades de las Plantas/parasitología , Enfermedades de las Plantas/terapia , Raíces de Plantas/citología , Raíces de Plantas/metabolismo , Raíces de Plantas/parasitología , Plasmodiophorida/crecimiento & desarrollo , Proto-Oncogenes Mas , Alineación de Secuencia , Esporas Protozoarias/efectos de los fármacos , Esporas Protozoarias/genética , Transcriptoma/efectos de los fármacos , Quinasas raf/genética
3.
Sci Rep ; 6: 36965, 2016 11 22.
Artículo en Inglés | MEDLINE | ID: mdl-27874080

RESUMEN

Plasmodiophora brassicae causes clubroot disease in cruciferous. In this report, lipid droplets were observed in the resting spores of P. brassicae. 295 lipid droplet-associated proteins were identified and categorized into nine groups. Transcriptome analysis of these proteins during three different zoosporic stages revealed differences in gene expression pattern. GO enrichment analysis revealed that these proteins associated with lipid droplets were mainly linked to biosynthesis and metabolism. GC-MS analysis revealed that lipid droplets contain seven types of free fatty acids: saturated fatty acids C16:0 and C18:0, and unsaturated fatty acids C18:1Δ9, C18:1Δ11, C18:2, C20:4 and C20:5. P. brassicae accumulated a large amount of triacylglycerols (TAGs). We systematically analyzed the putative proteins involved in TAG biosynthesis and its metabolic pathway. KEGG pathway analysis defined 3390 genes, including 167 genes involved in lipid metabolism. Transcriptome analysis revealed that 162 candidate enzymes involved in lipid metabolism were differential expressed. Our omics studies are the first to investigate the lipid droplet organelles in P. brassicae, providing a reference resource to study protist lipid droplets.


Asunto(s)
Gotas Lipídicas/química , Plasmodiophorida/metabolismo , Arabidopsis/parasitología , Ácidos Grasos no Esterificados/análisis , Cromatografía de Gases y Espectrometría de Masas , Perfilación de la Expresión Génica , Gotas Lipídicas/metabolismo , Metabolismo de los Lípidos/genética , Microscopía Electrónica de Transmisión , Proteómica , Proteínas Protozoarias/análisis , Proteínas Protozoarias/genética , Proteínas Protozoarias/metabolismo , Triglicéridos/análisis , Triglicéridos/biosíntesis
4.
Front Physiol ; 7: 402, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27679580

RESUMEN

Botrytis-induced kinase1 (BIK1), a receptor-like cytoplasmic kinase, plays an important role in resistance against pathogens and insects in Arabidopsis thaliana. However, it remains unknown whether BIK1 functions against Plasmodiophora brassicae, an obligate biotrophic protist that attacks cruciferous plants and induces gall formation on roots. Here, we investigated the potential roles of receptors FLS2, BAK1, and BIK1 in the infection of P. brassicae cruciferous plants. Wild-type plants, fls2, and bak1 mutants showed typical symptom on roots, and the galls were filled with large quantities of resting spores, while bik1 mutant plants exhibited strong resistance to P. brassicae. Compared with that of the wild-type plants, the root hair and cortical infection rate of bik1 mutant were significantly reduced by about 40-50%. A considerable portion of bik1 roots failed to form typical galls. Even if some small galls were formed, they were filled with multinucleate secondary plasmodia. The bik1 plants accumulated less reactive oxygen species (ROS) at infected roots than other mutants and wild-type plants. Exogenous salicylic acid (SA) treatment alleviated the clubroot symptoms in wild-type plants, and the expression of the SA signaling marker gene PR1 was significantly increased in bik1. Both sid2 (salicylic acid induction-deficient 2) and npr1-1 [non-expresser of PR genes that regulate systemic acquired resistance (SAR)] mutants showed increased susceptibility to P. brassicae compared with wild-type plants. These results suggest that the resistance of bik1 to P. brassicae is possibly mediated by SA inducible mechanisms.

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