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Open Access Research article

The dystrotelin, dystrophin and dystrobrevin superfamily: new paralogues and old isoforms

Hong Jin1, Sipin Tan1, Jane Hermanowski1, Sabrina Böhm1, Sabrina Pacheco2, Joanna M McCauley1, Marc J Greener1, Yaniv Hinits3, Simon M Hughes3, Paul T Sharpe2 and Roland G Roberts1*

Author Affiliations

1 Division of Genetics & Molecular Medicine, Department of Medical & Molecular Genetics, King's College London, Guy's Hospital, London SE1 9RT, UK

2 Department of Craniofacial Development, King's College London Dental Institute, Guy's Hospital, London SE1 9RT, UK

3 MRC Centre for Developmental Neurobiology and Randall Division of Cell and Molecular Biophysics, Guy's Campus, King's College London, London SE1 1UL, UK

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BMC Genomics 2007, 8:19  doi:10.1186/1471-2164-8-19

Published: 17 January 2007

Abstract

Background

Dystrophins and dystrobrevins are distantly related proteins with important but poorly understood roles in the function of metazoan muscular and neuronal tissues. Defects in them and their associated proteins cause a range of neuromuscular disorders. Members of this superfamily have been discovered in a relatively serendipitous way; we set out to compile a comprehensive description of dystrophin- and dystrobrevin-related sequences from available metazoan genome sequences, validated in representative organisms by RT-PCR, or acquired de novo from key species.

Results

Features of the superfamily revealed by our survey include: a) Dystrotelin, an entirely novel branch of the superfamily, present in most vertebrates examined. Dystrotelin is expressed in the central nervous system, and is a possible orthologue of Drosophila DAH. We describe the preliminary characterisation of its function, evolution and expression. b) A novel vertebrate member of the dystrobrevin family, γ-dystrobrevin, an ancient branch now extant only in fish, but probably present in our own ancestors. Like dystrophin, zebrafish γ-dystrobrevin mRNA is localised to myosepta. c) The extent of conservation of alternative splicing and alternative promoter use in the dystrophin and dystrobrevin genes; alternative splicing of dystrophin exons 73 and 78 and α-dystrobrevin exon 13 are conserved across vertebrates, as are the use of the Dp116, Dp71 and G-utrophin promoters; the Dp260 and Dp140 promoters are tetrapod innovations. d) The evolution of the unique N-terminus of DRP2 and its relationship to Dp116 and G-utrophin. e) A C-terminally truncated common ancestor of dystrophin and utrophin in cyclostomes. f) A severely restricted repertoire of dystrophin complex components in ascidians.

Conclusion

We have refined our understanding of the evolutionary history and isoform diversity of the five previously reported vertebrate superfamily members and describe two novel members, dystrotelin and γ-dystrobrevin. Dystrotelins, dystrophins and dystrobrevins are roughly equally related to each other. Vertebrates therefore have a repertoire of seven superfamily members (three dystrophins, three dystrobevins, and one dystrotelin), with one lost in tetrapods. Most invertebrates studied have one member from each branch. Although the basic shared function which is implied by the common architecture of these distantly related proteins remains unclear, it clearly permeates metazoan biology.