Abstract

BackgroundCrustaceans represent an attractive model to study biomineralization and cuticle matrix formation, as these events are precisely timed to occur at certain stages of the moult cycle. Moulting, the process by which crustaceans shed their exoskeleton, involves the partial breakdown of the old exoskeleton and the synthesis of a new cuticle. This cuticle is subdivided into layers, some of which become calcified while others remain uncalcified. The cuticle matrix consists of many different proteins that confer the physical properties, such as pliability, of the exoskeleton.ResultsWe have used a custom cDNA microarray chip, developed for the blue swimmer crab Portunus pelagicus, to generate expression profiles of genes involved in exoskeletal formation across the moult cycle. A total of 21 distinct moult-cycle related differentially expressed transcripts representing crustacean cuticular proteins were isolated. Of these, 13 contained copies of the cuticle_1 domain previously isolated from calcified regions of the crustacean exoskeleton, four transcripts contained a chitin_bind_4 domain (RR consensus sequence) associated with both the calcified and un-calcified cuticle of crustaceans, and four transcripts contained an unannotated domain (PfamB_109992) previously isolated from C. pagurus. Additionally, cryptocyanin, a hemolymph protein involved in cuticle synthesis and structural integrity, also displays differential expression related to the moult cycle. Moult stage-specific expression analysis of these transcripts revealed that differential gene expression occurs both among transcripts containing the same domain and among transcripts containing different domains.ConclusionThe large variety of genes associated with cuticle formation, and their differential expression across the crustacean moult cycle, point to the complexity of the processes associated with cuticle formation and hardening. This study provides a molecular entry path into the investigation of the gene networks associated with cuticle formation.

Highlights

  • Crustaceans represent an attractive model to study biomineralization and cuticle matrix formation, as these events are precisely timed to occur at certain stages of the moult cycle

  • Microarray expression analysis Custom P. pelagicus cDNA arrays were created using transcripts isolated from both whole crabs, and the brain, eyestalk, mandibular organ (MO) and Y-organ of crabs in the following five moult cycle stages: post-moult, intermoult, early pre-moult, late pre-moult, and ecdysis

  • A total of 13 unique cDNAs, each displaying differential expression profiles relating to moult stage, 3 x Post-moult (Cy3) vs Intermoult (Cy 5)

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Summary

Introduction

Crustaceans represent an attractive model to study biomineralization and cuticle matrix formation, as these events are precisely timed to occur at certain stages of the moult cycle. The process by which crustaceans shed their exoskeleton, involves the partial breakdown of the old exoskeleton and the synthesis of a new cuticle. This cuticle is subdivided into layers, some of which become calcified while others remain uncalcified. The cuticle matrix consists of many different proteins that confer the physical properties, such as pliability, of the exoskeleton Arthropods, such as arachnids, crustaceans and insects, represent the most abundant phylum in the animal kingdom. After ecdysis, during the post-moult stage, expansion of the partially formed new exoskeleton occurs followed by the tanning and mineralisation of the pre-ecdysial layers, and the deposition and hardening of the endocuticle. At the intermoult stage a mature, fully developed exoskeleton is formed [2]

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