Genome-wide identification and characterization of cytochrome P450 monooxygenase genes in the ciliate Tetrahymena thermophila
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* Corresponding author: Wei Miao miaowei530@yeah.net
1 Key Laboratory of Aquatic Biodiversity and Conservation, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, PR China
2 State Key Laboratory of Freshwater Ecology and Biotechnology, Institute of Hydrobiology, Chinese Academy of Sciences, Wuhan, 430072, PR China
3 Graduate School of Chinese Academy of Sciences, Beijing, 100049, PR China
BMC Genomics 2009, 10:208 doi:10.1186/1471-2164-10-208
Published: 1 May 2009Additional files
Additional file 1:
The position and orientation of three adjacent P450 genes (CYP5013A1, CYP5013C1 and CYP5013B1) in the T. thermophila genome. These three gene isoforms are tandemly located on scaffold 8254607. They were mistakenly merged into one "monster" gene by the TIGR gene finder as was shown in the Genome Browser map. Underline: the putative ORF of CYP5013A1 gene. Red italic: the first intron of CYP5013A1 gene. Green: the second intron of CYP5013A1 gene.
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Additional file 2:
Sequence alignment of the CYP5005A7 gene, ESTs, the pseudogene CYP5005A5P and the erroneous pseudogene TIGR_ CYP5005A7P. The CYP5005A7 gene sequence was obtained from the 2.1kb genomic DNA sequencing results. The two ESTs (TTL00012823 and EC269404) were retrieved from TBestDB and GenBank, respectively. The erroneous sites in the "TIGR_CYP5005A7P" sequence were indicated by red squares. The different sites between the CYP5005A7 gene and the pseudogene CYP5005A5P sequences were indicated by green squares.
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Additional file 3:
The unrooted maximum-likelihood (ML) tree of the T. thermophila P450 protein sequences. The resulting tree was tested with 200 bootstrap repeats with PhyML and the bootstrap values are indicated on each node.
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Additional file 4:
The conservation pattern of the T. thermophila P450 family. A: The full indication of the conservation pattern inferred by Consurf based on the multiple sequence alignment using mammalian P450 CYP3A4 as the template of secondary structure elements assignment. Bottom: key to the Consurf colours; B: The six putative substrate recognition sites (SRSs) region were indicated.
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Additional file 5:
Site-specific selection results of the CYP5005 and CYP5010 gene families. A: CYP5005 Family; B: CYP5010 Family. A seven-color scale was used by the Selecton program to represent different types of selection. Shades of yellow (colors 1 and 2) indicate ω > 1. Shades of white through magenta (colors 3 through 7) indicate various level of ω ≤ 1.
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Additional file 6:
Calculated values of the CYP5005 and CYP5010 gene families for each of nine different models. Calculated Akaike Information Criterion (AIC) and maximum-likelihood (ML) values of the CYP5005 and CYP5010 gene families for each of nine different models were listed. The results of best supported models under each cell conditions were marked in bold.
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Additional file 7:
Phylogenetic tree of the CYP5010 gene family and its expression profiles for the three physiological/developmental stages of the T. thermophila cells. Left: The ML tree of CYP5010 family used in the gene-expression evolution analysis. Relative branch lengths are proportional to number of substitutions per site. Right: The corresponding log2 transformed microarray data during three cellular conditions as a set of continuous data represent the character data at the taxa tips.
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Additional file 8:
Oligonucleotide primers used in this study.
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Additional file 9:
Codon usage parameters of 44 T. thermophila P450 genes. The CAI, ENc, GC content, GC12, GC3s and the RSCU values of the two most important axes were listed.
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