Email updates

Keep up to date with the latest news and content from BMC Genomics and BioMed Central.

Open Access Research article

LRRCE: a leucine-rich repeat cysteine capping motif unique to the chordate lineage

Hosil Park1, Julie Huxley-Jones13, Ray P Boot-Handford1, Paul N Bishop1, Teresa K Attwood2 and Jordi Bella1*

Author Affiliations

1 Wellcome Trust Centre for Cell-Matrix Research, Faculty of Life Sciences, University of Manchester, Manchester, M13 9PT, UK

2 Faculty of Life Sciences and School of Computer Science, University of Manchester, Manchester, M13 9PT, UK

3 Computational Biology, Molecular Discovery Research, GlaxoSmithKline Pharmaceuticals, Harlow, Essex, CM19 5AW, UK

For all author emails, please log on.

BMC Genomics 2008, 9:599  doi:10.1186/1471-2164-9-599

Published: 12 December 2008

Abstract

Background

The small leucine-rich repeat proteins and proteoglycans (SLRPs) form an important family of regulatory molecules that participate in many essential functions. They typically control the correct assembly of collagen fibrils, regulate mineral deposition in bone, and modulate the activity of potent cellular growth factors through many signalling cascades. SLRPs belong to the group of extracellular leucine-rich repeat proteins that are flanked at both ends by disulphide-bonded caps that protect the hydrophobic core of the terminal repeats. A capping motif specific to SLRPs has been recently described in the crystal structures of the core proteins of decorin and biglycan. This motif, designated as LRRCE, differs in both sequence and structure from other, more widespread leucine-rich capping motifs. To investigate if the LRRCE motif is a common structural feature found in other leucine-rich repeat proteins, we have defined characteristic sequence patterns and used them in genome-wide searches.

Results

The LRRCE motif is a structural element exclusive to the main group of SLRPs. It appears to have evolved during early chordate evolution and is not found in protein sequences from non-chordate genomes. Our search has expanded the family of SLRPs to include new predicted protein sequences, mainly in fishes but with intriguing putative orthologs in mammals. The chromosomal locations of the newly predicted SLRP genes would support the large-scale genome or gene duplications that are thought to have occurred during vertebrate evolution. From this expanded list we describe a new class of SLRP sequences that could be representative of an ancestral SLRP gene.

Conclusion

Given its exclusivity the LRRCE motif is a useful annotation tool for the identification and classification of new SLRP sequences in genome databases. The expanded list of members of the SLRP family offers interesting insights into early vertebrate evolution and suggests an early chordate evolutionary origin for the LRRCE capping motif.