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1.
BMC Genomics ; 12: 503, 2011 Oct 13.
Article in English | MEDLINE | ID: mdl-21995639

ABSTRACT

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.


Subject(s)
Oomycetes/genetics , Amino Acid Sequence , Brassicaceae/parasitology , Expressed Sequence Tags , Fungal Proteins/chemistry , Fungal Proteins/metabolism , Genome , Molecular Sequence Data , Plant Diseases/parasitology , Sequence Alignment , Sequence Analysis, RNA
2.
Mol Plant Microbe Interact ; 17(7): 711-9, 2004 Jul.
Article in English | MEDLINE | ID: mdl-15242165

ABSTRACT

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.


Subject(s)
Arabidopsis Proteins/genetics , Arabidopsis/genetics , Carboxylic Ester Hydrolases/genetics , DNA-Binding Proteins/genetics , Amino Acid Sequence , Arabidopsis/metabolism , Arabidopsis/microbiology , Arabidopsis Proteins/metabolism , Base Sequence , Carboxylic Ester Hydrolases/metabolism , Chromosomes, Artificial, Yeast , DNA-Binding Proteins/metabolism , Immunity, Innate/genetics , Molecular Sequence Data , Oomycetes/growth & development , Plant Diseases/genetics , Plant Diseases/microbiology , Sequence Homology, Amino Acid , Signal Transduction/genetics , Signal Transduction/physiology
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