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1.
BMC Genomics ; 12: 503, 2011 Oct 13.
Artigo em Inglês | MEDLINE | ID: mdl-21995639

RESUMO

BACKGROUND: Albugo candida is a biotrophic oomycete that parasitizes various species of Brassicaceae, causing a disease (white blister rust) with remarkable convergence in behaviour to unrelated rusts of basidiomycete fungi. RESULTS: A recent genome analysis of the oomycete Hyaloperonospora arabidopsidis suggests that a reduction in the number of genes encoding secreted pathogenicity proteins, enzymes for assimilation of inorganic nitrogen and sulphur represent a genomic signature for the evolution of obligate biotrophy. Here, we report a draft reference genome of a major crop pathogen Albugo candida (another obligate biotrophic oomycete) with an estimated genome of 45.3 Mb. This is very similar to the genome size of a necrotrophic oomycete Pythium ultimum (43 Mb) but less than half that of H. arabidopsidis (99 Mb). Sequencing of A. candida transcripts from infected host tissue and zoosporangia combined with genome-wide annotation revealed 15,824 predicted genes. Most of the predicted genes lack significant similarity with sequences from other oomycetes. Most intriguingly, A. candida appears to have a much smaller repertoire of pathogenicity-related proteins than H. arabidopsidis including genes that encode RXLR effector proteins, CRINKLER-like genes, and elicitins. Necrosis and Ethylene inducing Peptides were not detected in the genome of A. candida. Putative orthologs of tat-C, a component of the twin arginine translocase system, were identified from multiple oomycete genera along with proteins containing putative tat-secretion signal peptides. CONCLUSION: Albugo candida has a comparatively small genome amongst oomycetes, retains motility of sporangial inoculum, and harbours a much smaller repertoire of candidate effectors than was recently reported for H. arabidopsidis. This minimal gene repertoire could indicate a lack of expansion, rather than a reduction, in the number of genes that signify the evolution of biotrophy in oomycetes.


Assuntos
Oomicetos/genética , Sequência de Aminoácidos , Brassicaceae/parasitologia , Etiquetas de Sequências Expressas , Proteínas Fúngicas/química , Proteínas Fúngicas/metabolismo , Genoma , Dados de Sequência Molecular , Doenças das Plantas/parasitologia , Alinhamento de Sequência , Análise de Sequência de RNA
2.
Mol Plant Microbe Interact ; 17(7): 711-9, 2004 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-15242165

RESUMO

Resistance to Albugo candida isolate Acem1 is conferred by a dominant gene, RAC1, in accession Ksk-1 of Arabidopsis thaliana. This gene was isolated by positional cloning and is a member of the Drosophila toll and mammalian interleukin-1 receptor (TIR) nucleotide-binding site leucine-rich repeat (NB-LRR) class of plant resistance genes. Strong identity of the TIR and NB domains was observed between the predicted proteins encoded by the Ksk-1 allele and the allele from an Acem1-susceptible accession Columbia (Col) (99 and 98%, respectively). However, major differences between the two predicted proteins occur within the LRR domain and mainly are confined to the beta-strand/beta-turn structure of the LRR. Both proteins contain 14 imperfect repeats. RAC1-mediated resistance was analyzed further using mutations in defense regulation, including: pad4-1, eds1-1, and NahG, in the presence of the RAC1 allele from Ksk-1. White rust resistance was completely abolished by eds1-1 but was not affected by either pad4-1 or NahG.


Assuntos
Proteínas de Arabidopsis/genética , Arabidopsis/genética , Hidrolases de Éster Carboxílico/genética , Proteínas de Ligação a DNA/genética , Sequência de Aminoácidos , Arabidopsis/metabolismo , Arabidopsis/microbiologia , Proteínas de Arabidopsis/metabolismo , Sequência de Bases , Hidrolases de Éster Carboxílico/metabolismo , Cromossomos Artificiais de Levedura , Proteínas de Ligação a DNA/metabolismo , Imunidade Inata/genética , Dados de Sequência Molecular , Oomicetos/crescimento & desenvolvimento , Doenças das Plantas/genética , Doenças das Plantas/microbiologia , Homologia de Sequência de Aminoácidos , Transdução de Sinais/genética , Transdução de Sinais/fisiologia
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