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Open AccessResearch article

The fate of the duplicated androgen receptor in fishes: a late neofunctionalization event?

Véronique Douard1* email, Frédéric Brunet2* email, Bastien Boussau3 email, Isabelle Ahrens-Fath4 email, Virginie Vlaeminck-Guillem2 email, Bernard Haendler4 email, Vincent Laudet2 email and Yann Guiguen1 email

INRA-SCRIBE IFR 140, Campus de Beaulieu, 35042 Rennes Cedex, France

Institut de Génomique Fonctionnelle de Lyon, Université de Lyon, UMR 5242 du CNRS, INRA, IFR128 BioSciences Lyon-Gerland, Ecole Normale Supérieure de Lyon, 46, Allée d'Italie, 69364 Lyon Cedex 07, France

Biométrie et Biologie Évolutive UMR CNRS 5558 Université Claude Bernard-Lyon 1, 43, Boulevard du 11 novembre 1918, 69622 Villeurbanne Cedex, France

Bayer Schering Pharma AG, 13342 Berlin, Germany

author email corresponding author email* Contributed equally

BMC Evolutionary Biology 2008, 8:336doi:10.1186/1471-2148-8-336

Published: 18 December 2008

Additional files

Additional file 1:

ARs sequences alignment. Alignment of the DBD and LBD sequences of ARs compared to that of human (see Table 1 for accession numbers). In this alignment, a dot refers to the same aa as in the first sequence. Sequences not known in 5' and 3' are shown by a hyphen ("-") sign, as well as gaps. AR-B sequences are visualized by the grey background. Alignment with other non AR sequences are available upon request. In red are the gaps or insertions characterizing the ARs in fish. Amino acids shown in green are those conserved in divergent AR-B sequences whereas those in yellow are the substitutions characterizing all AR-Bs. Positions in blue are those specific to AR-A and those in violet are common to the actinopterygian ARs.

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Additional file 2:

Phylogenetic analyses of complete AR-A and AR-B. Phylogenetic analyses of complete AR-A and AR-B with sequences encompassing the DBD and the LBD. Four methods were used: bayesian with MrBayes, maximum likelihood (ML) with PhyML with 1000 bootstrap replicates; maximum parcimony (MP) and neighbor joining (NJ) as implemented in Seaview.

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Additional file 3:

Orthology relationships between medaka, tetraodon and zebrafish chromosomes. As referenced in legend Figure 4, these rose windows show the orthology relationship between chromosomes on which AR A and AR-B are located in the medaka, Tetraodon and the zebrafish. The excellent synteny observed between the chromosomes are strong remnants of the WGD that occurred specifically in the Teleost lineage. The red lines show the orthology link of the ARs among all the other orthologs (orthology based from Ensembl v48, in agreement with reciprocal best-hit analyses we performed, data not shown) shown here in green. (A) AR-A is found on chromosome T7 in the Tetraodon and on chromosome M14 in the medaka. A strong synteny is observed between these two chromosomes. (B) AR-B is found on chromosome T1 in the Tetraodon and on chromosome M10 in the medaka. A strong synteny is observed is also observed between these two chromosomes. (C) AR-A is found on chromosome Z5 in the zebrafish and on chromosome M14 in the medaka. An unequivocal synteny is observed between these two chromosomes, as shown in Figure 4-B between this zebrafish chromosome and that of the Tetraodon. (D) Although AR-B is found on chromosome M10 in the medaka and that a good synteny is observed with the chromosome Z14 in zebrafish, as observed in Figure 4-C for this species with the chromosome T1 of Tetraodon, the zebrafish lacks AR-B to the point we could not detect its pseudogene. (E) Table indicating the positions and Ensembl accession numbers of the relevant AR genes.

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Additional file 4:

Statistical distributions of the AR-A and AR-B substitutions in fish. Statistical representation of the distributions of the AR-A and AR-B substitutions in fish. The bell distribution is a random distribution of the substitutions, the diamond shows that the specificity of AR-A and AR-B versus the other AR is statistically clearly not random.

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Additional file 5:

Human and fish substitutions along the DBD of the human AR. Representation of the DBD of the human AR modified from [77]. The aa in green are the ones specific to AR-B; in blue, the ones specific to AR-A; in orange and red, when respectively the aa is hit by a common substitution or a different one when compared to other vertebrate ARs. Arrowheads refer to mutations found in CAIS, PAIS, MAIS and prostate cancer respectively in color pink, orange, blue and black. Different aa substitutions are shown by arrowheads side by side.

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Additional file 6:

List of human substitutions in AR leading to AIS phenotypes and prostate cancer. List of substitutions in human AR leading to CAIS, PAIS, MAIS and prostate cancer phenotype, as referenced into Bruce Gottlieb's database (androgendb.mcgill.ca/AR23C.pdf) [75], and list of the AR-A and AR-B specific substitutions detailed in Additional file 1.

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Additional file 7:

Detailed analysis of Table 2.

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