Structural Basis of Dscam Isoform Specificity.
From: Department of Medical Oncology, Dana-Farber Cancer Institute, Boston, Massachusetts 02115, USA.
Nature
- Publish Date: Sep 2007
- ISSN: 1476-4687
- Volume: 449
- Issue: 7161
- Pages: 487-91
- Medium: Internet
- Language: English
- Citation (JAMA): Meijers Rob, Puettmann-Holgado Roland, Skiniotis Georgios, et al. Structural Basis of Dscam Isoform Specificity.. Nature Sep 2007;449:487-91
Abstract
The Dscam gene gives rise to thousands of diverse cell surface receptors thought to provide homophilic and heterophilic recognition specificity for neuronal wiring and immune responses. Mutually exclusive splicing allows for the generation of sequence variability in three immunoglobulin ecto-domains, D2, D3 and D7. We report X-ray structures of the amino-terminal four immunoglobulin domains (D1-D4) of two distinct Dscam isoforms. The structures reveal a horseshoe configuration, with variable residues of D2 and D3 constituting two independent surface epitopes on either side of the receptor. Both isoforms engage in homo-dimerization coupling variable domain D2 with D2, and D3 with D3. These interactions involve symmetric, antiparallel pairing of identical peptide segments from epitope I that are unique to each isoform. Structure-guided mutagenesis and swapping of peptide segments confirm that epitope I, but not epitope II, confers homophilic binding specificity of full-length Dscam receptors. Phylogenetic analysis shows strong selection of matching peptide sequences only for epitope I. We propose that peptide complementarity of variable residues in epitope I of Dscam is essential for homophilic binding specificity.
Mesh Headings (Keywords): Alternative Splicing, Amino Acid Sequence, Animals, Binding Sites, Crystallography, X-Ray, Dimerization, Drosophila Proteins, Drosophila melanogaster, Exons, Models, Molecular, Molecular Sequence Data, Protein Isoforms, Protein Structure, Quaternary, Protein Structure, Tertiary, Structure-Activity Relationship, Substrate Specificity
Check for Full Text / PubMed Unique Identifier (PMID): 17721508
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