Abstract

BackgroundInsects evolved ingenious adaptations to use extraordinary food sources. Particularly, the diet of herbivores enriched with noxious plant secondary metabolites requires detoxification mechanisms. Sequestration, which involves the uptake, transfer, and concentration of occasionally modified phytochemicals into specialized tissues or hemolymph, is one of the most successful detoxification strategies found in most insect orders. Due to the ability of ATP-binding cassette (ABC) carriers to transport a wide range of molecules including phytochemicals and xenobiotics, it is highly likely that they play a role in this sequestration process. To shed light on the role of ABC proteins in sequestration, we describe an inventory of putative ABC transporters in various tissues in the sequestering juvenile poplar leaf beetle, Chrysomela populi.ResultsIn the transcriptome of C. populi, we predicted 65 ABC transporters. To link the proteins with a possible function, we performed comparative phylogenetic analyses with ABC transporters of other insects and of humans. While tissue-specific profiling of each ABC transporter subfamily suggests that ABCB, C and G influence the plant metabolite absorption in the gut, ABCC with 14 members is the preferred subfamily responsible for the excretion of these metabolites via Malpighian tubules. Moreover, salicin, which is sequestered from poplar plants, is translocated into the defensive glands for further deterrent production. In these glands and among all identified ABC transporters, an exceptionally high transcript level was observed only for Cpabc35 (Cpmrp). RNAi revealed the deficiency of other ABC pumps to compensate the function of CpABC35, demonstrating its key role during sequestration.ConclusionWe provide the first comprehensive phylogenetic study of the ABC family in a phytophagous beetle species. RNA-seq data from different larval tissues propose the importance of ABC pumps to achieve a homeostasis of plant-derived compounds and offer a basis for future analyses of their physiological function in sequestration processes.

Highlights

  • Lipid bilayers form efficient barriers for cellular partitioning

  • The core functional unit of ATP-binding cassette (ABC) proteins consists of four domains: two cytoplasmic domains containing the highly conserved nucleotidebinding domains (NBDs), which are responsible for the ATP hydrolysis needed to provide energy for the transport cycle, and two transmembrane domains (TMDs), each in most cases composed of six membrane-spanning helices, which impart substrate specificity and translocation [2,3,4]

  • We focused on the distribution of ABC transporters in the different tissues of juvenile C. populi to assign a function to each transcript related to a certain tissue

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Summary

Introduction

Lipid bilayers form efficient barriers for cellular partitioning The translocation across these membranous barriers is crucial for many aspects of cell physiology, including the uptake of nutrients, the elimination of waste products, or energy generation and cell signaling. The ATP-binding cassette (ABC) transporters constitute one of the largest families of membrane translocators [1]. The core functional unit of ABC proteins consists of four domains: two cytoplasmic domains containing the highly conserved nucleotidebinding domains (NBDs), which are responsible for the ATP hydrolysis needed to provide energy for the transport cycle, and two transmembrane domains (TMDs), each in most cases composed of six membrane-spanning helices, which impart substrate specificity and translocation [2,3,4]. Due to the ability of ATP-binding cassette (ABC) carriers to transport a wide range of molecules including phytochemicals and xenobiotics, it is highly likely that they play a role in this sequestration process. To shed light on the role of ABC proteins in sequestration, we describe an inventory of putative ABC transporters in various tissues in the sequestering juvenile poplar leaf beetle, Chrysomela populi

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