Frank M. Horodyski

Insect allatotropins belong to a family of structurally-related myoactive peptides present in several invertebrate phyla

Originally named for its ability to stimulate juvenile hormone production by lepidopteran corpora allata, allatotropin has emerged as a neuropeptide with multiple neural, endocrine and myoactive roles. This paper describes the experimental evidence for allatotropin action, its localization in several species of insects, and its multiple effects on a variety of different tissues that lead to increased hemolymph circulation and gut motility. The overall physiological effects may also include species-specific effects such as the regulation of nutrient absorption, modulation of the circadian cycle and migratory preparedness. In addition, we present evidence suggesting that allatotropins are members of a family of myoactive peptides found in several invertebrate phyla. Finally, we speculate that the myoactive properties of allatotropins are basal and it is likely that the stimulatory action of allatotropins on juvenile hormone synthesis evolved secondarily.

Molecular Characterization of the Insect Immune Protein Hemolin and its High Induction During Embryonic Diapause in the Gypsy Moth, Lymantria dispar

During the embryonic (pharate first instar) diapause of the gypsy moth, Lymantria dispar, a 55 kDa protein is highly up-regulated in the gut. We now identify that protein as hemolin, an immune protein in the immunoglobulin superfamily. We isolated a gypsy moth hemolin cDNA and demonstrated a high degree of similarity with hemolins from three other moth species. Hemolin mRNA levels increased at the time of diapause initiation and remained high throughout the mandatory period of chilling required to terminate diapause in this species, and then dropped in late diapause. This mRNA pattern reflects the pattern of protein synthesis. These results suggest that hemolin is developmentally up-regulated in the gut during diapause. Diapause in this species can be prevented using KK-42, an imidazole derivative known to inhibit ecdysteroid biosynthesis, and gypsy moths treated in this manner failed to elevate hemolin mRNA. Conversely, this diapause appears to be initiated and maintained by the steroid hormone, 20-hydroxyecdysone, and the addition of 20-hydroxyecdysone to the culture medium elevated hemolin mRNA in the gut. Our results thus indicate a role for 20-hydroxyecdysone in the elevation of hemolin mRNA during diapause. Presumably, hemolin functions to protect the gypsy moth from microbial infection during its long, overwintering diapause.

Biological activity of Manduca sexta allatotropin-like peptides, predicted products of tissue-specific and developmentally regulated alternatively spliced mRNAs

The insect neuropeptide, allatotropin (Manse-AT), exerts multiple functions including the stimulation of juvenile hormone (JH) biosynthesis in adults and the inhibition of active ion transport across the midgut epithelium of feeding larvae. The Manse-AT gene is expressed in multiple regions of the nervous system as three mRNAs that differ by alternative splicing. The specific mRNA isoform present differs in a tissue- and developmental-specific manner thus providing a mechanism for the regulated production of peptides specific to each isoform. These peptides are predicted to include three allatotropin-like (Manse-ATL) peptides that exhibit limited structural identity to Manse-AT and overlapping biological activities.

Alternative splicing of transcripts expressed by the Manduca sexta allatotropin (Mas-AT) gene is regulated in a tissue-specific manner<

The Manduca allatotropin (Mas-AT) gene is expressed as at least three mRNA isoforms that differ from each other by alternative splicing. The location at which the alternative exons are included in the mature mRNAs occur within the open reading frame, so that three different propeptides are predicted as translation products. In the pharate adult insect, the major mRNA isoform expressed in the brain and frontal ganglion differs from that expressed in the nerve cord. Examination of the deduced translations of the alternative exons reveals the presence of three additional Mas-AT-like sequences that are flanked by basic amino acid residues. Therefore, the Mas-AT-like sequences present within the gene may be derived from a duplication of an ancestral Mas-AT-like sequence followed by divergence.

EXPRESSION OF THE MANDUCA SEXTA ALLATOTROPIN GENE IN CELLS OF THE CENTRAL AND ENTERIC NERVOUS SYSTEMS

Manduca sexta allatotropin (Mas‐AT) was isolated and first characterized as a peptide that stimulated juvenile hormone biosynthesis in adult lepidopteran corpora allata and was subsequently shown to have cardioacceleratory activity in the pharate adult. In this study, we identified the cells in the nervous system of the insect that contain mRNA encoding Mas‐AT and immunoreactivity against a polyclonal antiserum to Mas‐AT. In larvae, Mas‐AT mRNA and immunoreactivity was most abundant in two cells in the frontal ganglion, which project their axons down the recurrent nerve toward the gut, and in cells in the terminal abdominal ganglion. Lower levels of Mas‐AT mRNA were detected in the brain and subesophageal ganglion. In the pupal and pharate adult stages, we detected Mas‐AT mRNA and immunoreactivity in cells of the abdominal ganglia and in additional cells in the terminal abdominal ganglion. These additional cells in the ventral nerve cord that express Mas‐AT during the pupal and pharate adult stages include cells that differentiate during metamorphosis as well as cells that exist in larvae but do not begin to express Mas‐AT until these later developmental stages. Some of the cells that exhibit Mas‐AT immunoreactivity lack Mas‐AT mRNA, suggesting that the antisera used in this and previous studies recognizes other peptides in addition to Mas‐AT. This pattern of expression suggests that Mas‐AT may mediate multiple physiological functions during the life cycle of the insect, including the larval stage in which no function has yet been described for the peptide. J. Comp. Neurol. 403:407–420, 1999.

Molecular Characterization and Cell- Specific Expression of a Manduca sexta FLRFamide Gene

FMRFamide‐related peptides (FaRPs) are a large group of neuropeptides containing a common RFamide C‐terminus; they have been identified in vertebrates and invertebrates. We have isolated the cDNA that encodes three FaRPs in the tobacco hornworm, Manduca sexta, including the amidated decapeptide F10. The larger FaRPs are the partially processed precursors of F10, a neuropeptide belonging to the myosuppressin family of peptides. The presence of all three FaRPs in different tissues suggests differential utilization of typical dibasic processing sites and atypical processing sites C‐terminal to leucine residues. F10 mRNA was detected in the brain, nerve cord, and midgut, and the mRNA levels in the nervous system are dynamically regulated during development. In situ hybridization analysis localized the F10 mRNA to a variety of cell types within the central nervous system (CNS), a peripheral neurosecretory cell (L1), and midgut endocrine cells, which suggests diverse functions. Distribution of the F10‐containing neurons within the central nervous system is segment‐specific, and the developmental profile suggests that the F10 gene products may have stage‐specific functions. Molecular characterization of the F10 gene has provided insights into its regulation and cell‐specific distribution that will enhance our understanding of how these FaRPs modulate different physiological systems and ultimately behavior. J. Comp. Neurol. 446:377–396, 2002.

Isolation and functional characterization of an allatotropin receptor from Manduca sexta.

Manduca sexta allatotropin (Manse-AT) is a multifunctional neuropeptide whose actions include the stimulation of juvenile hormone biosynthesis, myotropic stimulation, cardioacceleratory functions, and inhibition of active ion transport. Manse-AT is a member of a structurally related peptide family that is widely found in insects and also in other invertebrates. Its precise role depends on the insect species and developmental stage. In some lepidopteran insects including M. sexta, structurally-related AT-like (ATL) peptides can be derived from alternatively spliced mRNAs transcribed from the AT gene. We have isolated a cDNA for an AT receptor (ATR) from M. sexta by a PCR-based approach using the sequence of the ATR from Bombyx mori. The sequence of the M. sexta ATR is similar to several G protein-coupled receptors from other insect species and to the mammalian orexin receptor. We demonstrate that the M. sexta ATR expressed in vertebrate cell lines is activated in a dose-responsive manner by Manse-AT and each Manse-ATL peptide in the rank order ATL-I > ATL-II > ATL-III > AT, and functional analysis in multiple cell lines suggest that the receptor is coupled through elevated levels of Ca(2+) and cAMP. In feeding larvae, Manse-ATR mRNA is present at highest levels in the Malpighian tubules, followed by the midgut, hindgut, testes, and corpora allata, consistent with its action on multiple target tissues. In the adult corpora cardiaca--corpora allata complex, Manse-ATR mRNA is present at relatively low levels in both sexes.

Neuroendocrine control of insect ecdysis by eclosion hormone

Abstract The peptides eclosion hormone (EH) and ecdysis-triggering hormone (ETH) trigger ecdysis behaviors and other physiological changes which occur at the end of the molt. EH is synthesized in a discrete set of cerebral neurosecretory cells, and is released into the central nervous system and into the hemolymph in response to the declining ecdysteroid titers. The onset of behavioral sensitivity to EH action is similarly controlled by ecdysteroids. EH is released from the ventral nerve cord for larval and pupal ecdyses, and from the corpora cardiaca for adult ecdysis. This transition is mediated by the restructuring of the EH cells during adult development, so that they elaborate an axon which extends to the CC for storage and release of EH just prior to adult ecdysis. ETH is released from the Inka cells, a component of the segmentally paired epitracheal glands, and acts directly on the central nervous system (CNS) to trigger preecdysis and ecdysis behavior. Although EH is best understood in lepidopteran insects, accumulating evidence suggests that EH is present in all insects and may provide a general hormonal mechanism to regulate ecdysis.

Restriction of nutrient intake results in the increase of a specific Manduca sexta allatotropin (Manse-AT) mRNA in the larval nerve cord.

The Manduca allatotropin (Manse-AT) gene is expressed as three mRNAs that differ from each other by alternative splicing. The level of one of these mRNAs (RNA-3) is specifically increased in the nerve cord of last instar larvae that were starved, parasitized, or fed the ecdysteroid agonist RH-5992. Each of these treatments results in reduction of feeding and increased levels of juvenile hormone (JH). The normal decline in JH biosynthesis by the corpora allata does not occur in starved or RH-5992-fed larvae. The increase in RNA-3 levels has the capacity to increase the production of Manse-AT and two related peptides that may be part of the complex response of larvae to nutrient deprivation.

Effects of starvation and mating on corpora allata activity and allatotropin (Manse-AT) gene expression in Manduca sexta.

The levels of three alternatively spliced mRNAs from the Manduca sexta allatotropin (Manse-AT) gene were determined following physiological manipulations during the larval, pupal and adult stages; starvation of larvae, induction of pupal diapause and adult mating experience. The juvenile hormone biosynthetic activity of the corpora allata (CA) was also determined in starved larvae and in mated and unmated females. Starvation of early fifth instar larvae specifically increased the amount of one Manse-AT mRNA that is predicted to encode Manse-AT and two related peptides, Manse-ATL-I and -II. The normal rapid decrease in the activity of the CA in last instar larvae was not observed in starved insects which maintained a relatively high rate of JH biosynthesis for at least 3 days. Diapause induction resulted in a small increase in one Manse-AT mRNA, but levels were much lower compared to those observed in larvae or adults. During the first 4 days of adult life, Manse-AT mRNA levels were not changed as a result of mating. However, in mated females, the rate of JH biosynthesis gradually increased, in sharp contrast to the relatively low level of CA activity seen in virgin females. These observations suggest the elevated activity of the CA in mated females is not simply due to the increased level of Manse-AT mRNA.