Abstract
A family of evolutionarily old hormones is the glycoprotein cysteine knot-forming heterodimers consisting of alpha- (GPA) and beta-subunits (GPB), which assemble by noncovalent bonds. In mammals, a common glycoprotein hormone alpha-subunit (GPA1) pairs with unique beta-subunits that establish receptor specificity, forming thyroid stimulating hormone (GPA1/TSHβ) and the gonadotropins luteinizing hormone (GPA1/LHβ), follicle stimulating hormone (GPA1/FSHβ), choriogonadotropin (GPA1/CGβ). A novel glycoprotein heterodimer was identified in vertebrates by genome analysis, called thyrostimulin, composed of two novel subunits, GPA2 and GPB5, and homologs occur in arthropods, nematodes and cnidarians, implying that this neurohormone system existed prior to the emergence of bilateral metazoans. In order to discern possible physiological roles of this hormonal signaling system in mosquitoes, we have isolated the glycoprotein hormone genes producing the alpha- and beta-subunits (AedaeGPA2 and AedaeGPB5) and assessed their temporal expression profiles in the yellow and dengue-fever vector, Aedes aegypti. We have also isolated a putative receptor for this novel mosquito hormone, AedaeLGR1, which contains features conserved with other glycoprotein leucine-rich repeating containing G protein-coupled receptors. AedaeLGR1 is expressed in tissues of the alimentary canal such as the midgut, Malpighian tubules and hindgut, suggesting that this novel mosquito glycoprotein hormone may regulate ionic and osmotic balance. Focusing on the hindgut in adult stage A. aegypti, where AedaeLGR1 was highly enriched, we utilized the Scanning Ion-selective Electrode Technique (SIET) to determine if AedaeGPA2/GPB5 modulated cation transport across this epithelial tissue. Our results suggest that AedaeGPA2/GPB5 does indeed participate in ionic and osmotic balance, since it appears to inhibit natriuresis and promote kaliuresis. Taken together, our findings imply this hormone may play an important role in ionic balance when levels of Na+ are limited and levels of K+ are in excess – such as during the digestion and assimilation of erythrocytes following vertebrate blood-feeding by females.
Highlights
In mammals, classic heterodimeric glycoprotein hormones include the pituitary and placental gonadotropins luteinizing hormone (LH), follicle-stimulating hormone (FSH) and choriogonadotropin (CG) along with thyroid-stimulating hormone (TSH) [1]
The A. aegypti GPA2 (AedaeGPA2) cDNA was compared to the genomic data and revealed that the AedaeGPA2 gene contains at least two exons and spans over 14.7 kb of the genome
AedaeLGR1 In order to provide further evidence for inferring possible physiological activities governed by this glycoprotein hormone signaling system in the mosquito, we examined expression in all post-embryonic stages and tissue-specific expression in selected adult alimentary canal tissues for the prospective A. aegypti GPA2/ GPB5 receptor, AedaeLGR1
Summary
Classic heterodimeric glycoprotein hormones include the pituitary and placental gonadotropins luteinizing hormone (LH), follicle-stimulating hormone (FSH) and choriogonadotropin (CG) along with thyroid-stimulating hormone (TSH) [1]. These hormones share a common alpha subunit, glycoprotein A (GPA1), and each contains a unique beta subunit, glycoprotein B (GPB1-4), which confers receptor specificity. A little over a decade ago, genome screening revealed the existence of another heterodimeric glycoprotein hormone, thyrostimulin, which consists of novel alpha (GPA2) and beta (GPB5) subunits [2]. With the recent discovery of two novel subunits forming an additional heterodimeric glycoprotein hormone in mammals, similar glycoprotein hormone forming subunits have been identified in insects [2,6]. An elegant study using the fruit fly genetic toolbox revealed that the glycoprotein hormone subunits are most highly expressed in a bilateral pair of neuroendocrine cells within each of the first four abdominal neuromeres in both larvae and adults [7]
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