Abstract

Simple SummaryGenitalia and reproduction-associated proteins are often species-specific and might evolve rapidly. The situation in which the morphology of the reproductive system is the only difference between two or several closely related species has been reported on multiple occasions. Nevertheless, the reasons for such rapid divergence of the reproductive system is still poorly investigated. To shed some light on the issue, we performed a transcriptomic and proteomic comparison of pallial oviducts from the two sibling species of gastropods Littorina obtusata and L. fabalis. The main identified differences were associated with three functional groups of genes: transposable elements, which enhance genome variation and promote the evolution of new genes, receptor proteins potentially involved in friend or foe recognition, and various enzymes. We hypothesize that these functional groups reflect both the mechanism (transposable elements) and the directions (friend or foe recognition and reproductive physiology) of the rapid evolution of the reproductive system.Genus Littorina subgenus Neritrema (Mollusca, Caenogastropoda) includes the “obtusata” group of closely related species (Littorina obtusata and L. fabalis). The anatomy of the adult reproductive system (pallial oviduct) is the only reliable feature used for species identification in females of these species. Reproductive system anatomy and reproduction-associated proteins often diverge between sibling species. Despite being of high evolutionary interest, the molecular basis of this divergence remains poorly understood. We performed proteotranscriptomic comparison of oviducts of L. obtusata and L. fabalis by RNA-seq on Illumina HiSeq 2500 and two-dimensional protein electrophoresis (2D DIGE) with MS/MS identification of the species-specific proteins. The interspecies differences in the oviduct were associated with (1) metabolic proteins reflecting overall physiological differences between L. obtusata and L. fabalis, (2) receptor proteins, and (3) transcripts related to transposable elements (TEs). Various receptors identified may recognize a wide variety of ligands from pathogen-associated molecular patterns to specific carbohydrates on the sperm surface. Therefore, these may participate in immune defense as well as in sperm storage and regulation. Species-specificity of multiple TE sequences (coding for reverse transcriptase and ribonuclease H) may indicate the important role of these genomic elements in the Littorina species divergence, which has not been reported previously.

Highlights

  • Littorina obtusata (Linnaeus 1758) and L. fabalis (Turton 1825) are sibling species of the genus Littorina subgenus Neritrema (Mollusca, Caenogastropoda) which are referred to as the cryptic “obtusata” group [1]

  • L. fabalis and L. obtusata are known to vary significantly in their shell morphology, but the anatomy of the adult reproductive system is the definitive character for species discrimination: number and position of the penial mamilliform glands (PMGs), the penial filament shape in males, and the shape of the bursa copulatrix of the pallial oviduct in females [1]

  • 46,098,082 and 56,983,594 clean reads were obtained for two pooled biological replicates of L. obtusata and L. fabalis, respectively

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Summary

Introduction

Littorina obtusata (Linnaeus 1758) and L. fabalis (Turton 1825) are sibling species of the genus Littorina subgenus Neritrema (Mollusca, Caenogastropoda) which are referred to as the cryptic “obtusata” group [1]. L. fabalis and L. obtusata are known to vary significantly in their shell morphology, but the anatomy of the adult reproductive system is the definitive character for species discrimination: number and position of the penial mamilliform glands (PMGs), the penial filament shape in males, and the shape of the bursa copulatrix of the pallial oviduct in females [1]. PMGs are specific glands found in the penises of all species of the Littorina genus. These glands have several types of secretory cells, but their exact function is still unknown [1]. The jelly gland includes a bursa (insemination site), which is connected with a receptacle (sperm storage site) by the sperm groove [1]

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