Comparative EST analysis provides insights into the basal aquatic fungus Blastocladiella emersonii

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Abstract

Background: Blastocladiella emersonii is an aquatic fungus of the Chytridiomycete class, which is at the base of the fungal phylogenetic tree. In this sense, some ancestral characteristics of fungi and animals or fungi and plants could have been retained in this aquatic fungus and lost in members of late-diverging fungal species. To identify in B. emersonii sequences associated with these ancestral characteristics two approaches were followed: (1) a large-scale comparative analysis between putative unigene sequences (uniseqs) from B. emersonii and three databases constructed ad hoc with fungal proteins, animal proteins and plant unigenes deposited in Genbank, and (2) a pairwise comparison between B. emersonii full-length cDNA sequences and their putative orthologues in the ascomycete Neurospora crassa and the basidiomycete Ustilago maydis. Results: Comparative analyses of B. emersonii uniseqs with fungi, animal and plant databases through the two approaches mentioned above produced 166 B. emersonii sequences, which were identified as putatively absent from other fungi or not previously described. Through these approaches we found: (1) possible orthologues of genes previously identified as specific to animals and/or plants, and (2) genes conserved in fungi, but with a large difference in divergence rate in B. emersonii. Among these sequences, we observed cDNAs encoding enzymes from coenzyme B12-dependent propionyl-CoA pathway, a metabolic route not previously described in fungi, and validated their expression in Northern blots. Conclusion: Using two different approaches involving comparative sequence analyses, we could identify sequences from the early-diverging fungus B. emersonii previously considered specific to animals or plants, and highly divergent sequences from the same fungus relative to other fungi. © 2006 Ribichich et al; licensee BioMed Central Ltd.

Figures

  • Table 1: Putative identification of 105 B. emersonii-animal shared sequences.
  • Table 1: Putative identification of 105 B. emersonii-animal shared sequences. (Continued)
  • Table 1: Putative identification of 105 B. emersonii-animal shared sequences. (Continued)
  • Table 2: Putative identification of 20 B. emersonii-plant shared sequences. See legend of Table 1 for details of the notes.
  • Table 3: Distribution of syntaxin family members in different main groups of organisms. The column with B. emersonii heading indicates the presence (yes) or absence (not found yet) of ESTs encoding the respective syntaxins in our libraries. SNARE proteins (including syntaxins) have been reclassified in two groups divided into five classes (see [41] and ref. there in). We have maintained the distribution according Sanderfoot et al. [24] to facilitate the comparison with our data.
  • Table 4: Putative identification of 37 B. emersonii-animal-plant shared sequences. See legend of Table 1 for details of the notes.
  • Table 5: Selected divergent and conserved orthologs from B. emersonii according to pairwise bit score plots. ΔS' = difference in bit score value. For each comparison plus and minus signs represent conserved and divergent B. emersonii sequences, respectively. Black circles identify a difference between N. crassa or U. maydis and B. emersonii scores when compared to animal or plant sequences (Nc A, Nc P, Um A and Um P, respectively). The database accession numbers below the circles correspond to sequences from N. crassa/U. maydis and animal/plant putative orthologs in each comparison. Data were selected from the plot in figure 3 and re-evaluated by comparison with other fungal vs. animal/plant scores. Database assembled sequences or accession numbers of B. emersonii and animal/plant putative orthologous sequences (same order as shown in the table) are: B. emersonii, [BeDB:BeAS1253, BeAS1274, BeAS745, and BeAS895]; animal data, [Genbank:DAA01331, AAB00075, AK060330, and EMBL: CAF97202]; plant data, [Genbank: AK062838, AK110624, and AK073448]
  • Table 6: Fungal expressed sequences used for constructing the two ad hoc fungal databases. Two new protein and nucleotide databases were used to filter out sequences not previously matched with fungal data belonging to the original fungal database. The nucleotide database included only unigenes, ESTs and mitochondrial sequences.

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Ribichich, K. F., Georg, R. C., & Gomes, S. L. (2006). Comparative EST analysis provides insights into the basal aquatic fungus Blastocladiella emersonii. BMC Genomics, 7. https://doi.org/10.1186/1471-2164-7-177

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