Abstract

Scarab beetles exhibit an astonishing variety of rigid exo-skeletal outgrowths, known as “horns”. These traits are often sexually dimorphic and vary dramatically across species in size, shape, location, and allometry with body size. In many species, the horn exhibits disproportionate growth resulting in an exaggerated allometric relationship with body size, as compared to other traits, such as wings, that grow proportionately with body size. Depending on the species, the smallest males either do not produce a horn at all, or they produce a disproportionately small horn for their body size. While the diversity of horn shapes and their behavioural ecology have been reasonably well studied, we know far less about the proximate mechanisms that regulate horn growth. Thus, using 454 pyrosequencing, we generated transcriptome profiles, during horn growth and development, in two different scarab beetle species: the Asian rhinoceros beetle, Trypoxylus dichotomus, and the dung beetle, Onthophagus nigriventris. We obtained over half a million reads for each species that were assembled into over 6,000 and 16,000 contigs respectively. We combined these data with previously published studies to look for signatures of molecular evolution. We found a small subset of genes with horn-biased expression showing evidence for recent positive selection, as is expected with sexual selection on horn size. We also found evidence of relaxed selection present in genes that demonstrated biased expression between horned and horn-less morphs, consistent with the theory of developmental decoupling of phenotypically plastic traits.

Highlights

  • Evolution has generated a spectacular array of secondary sexually selected traits [1], with the most well known examples including the peacock’s train [2], antlers on cervids [3], and brightly coloured dewlaps of the anole lizard [4]

  • Several key issues need to be addressed, including: understanding how exaggerated growth of traits arise, and how final trait size is modulated in response to the physiological condition of males [10]; as well as understanding how exaggerated traits are developmentally related to other traits, which is especially important when exaggerated structures are novel structures (e. g. what common pathways have been co-opted into the development of the novel trait?) [11,12]

  • Using the transcriptome sequences generated here, we investigate the molecular evolution of genes involved in horn development from two contexts: sexual selection and developmental decoupling [28,36,37]

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Summary

Introduction

Evolution has generated a spectacular array of secondary sexually selected traits [1], with the most well known examples including the peacock’s train [2], antlers on cervids [3], and brightly coloured dewlaps of the anole lizard [4]. These exaggerated traits tend to be most prominent in males and can affect female preference, or be used as weapons to determine the outcome of male-male conflict. Several key issues need to be addressed, including: understanding how exaggerated growth of traits arise, and how final trait size is modulated in response to the physiological condition of males [10]; as well as understanding how exaggerated traits are developmentally related to other traits, which is especially important when exaggerated structures are novel structures (e. g. what common pathways have been co-opted into the development of the novel trait?) [11,12]

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