Ecdysis triggering hormone signaling in the yellow fever mosquito Aedes aegypti (original) (raw)

Mosquito ecdysteroid receptor: Analysis of the cDNA and expression during vitellogenesis

Insect Biochemistry and Molecular Biology, 1995

An insect steroid hormone, 20-hydroxyecdysone (20E), plays an important role in regulating egg maturation in mosquitoes. To better understand its role, we cloned the cDNA coding for the putative ecdysteroid receptor from the mosquito, Aedes aegypti (AaEcR). The 4158 hp AaEcR cDNA has an open reading frame of 675 amino acids with 10 potential glycosylation sites and a putative phosphorylation polyserine domain. The AaEcR has a DNA binding domain with two zinc fingers and a ligand binding domain characteristic of members of the steroid hormone receptor superfamily. These AaEcR domains share 97 and 87% identities with the respective domains of the Drosophila ecdysteroid receptor (DmEcR). However, the A/B region of the AaEcR shares 35% identity with that of DmEcR-Bl isoform. The F region, located at the carboxyl-terminal of the AaEcR, has only 9% identity with the corresponding region of DmEcR. Potential nuclear targeting and dimerization signals are also present in the AaEcR sequence. There are three AaEcR transcripts of 4.2 kb, 6 kb and 11 kb in adult mosquitoes. 4.2 kb mRNA is predominantly expressed in female mosquitoes during vitellogenesis. In both the fat body and ovaries of the female mosquito, the level of AaEcR mRNA is high at the previtellogenic period and after the onset of vitellogenesis (6 h post blood meal, PBM). Aedes aegypti Fat body Ovary Steroid receptor Ecdysone 1NTRODUCTION Steroid hormones and their receptors are important regulatory molecules controlling a wide array of essential functions in both lower and higher eukaryotes. For vertebrates, a wealth of information has been accumulated concerning the mode of action of steroid hormones, their interaction with receptors and target genes. Along with receptors for thyroid hormone, retinoic acid, and vitamin D, steroid hormone receptors form a family of hormoneregulated transcription factors, known as the steroid receptor superfamily (Evans, 1988; Green and Chambon, 1988; Beato, 1989). The key steroid hormone in arthropods is 20-hydroxyecdysone (20E). It regulates developmental processes such as molting, metamorphosis, and reproduction (Riddiford,

Ecdysteroid titers and developmental expression of ecdysteroid-regulated genes during metamorphosis of the yellow fever mosquito, Aedes aegypti (Diptera: Culicidae)

Journal of Insect Physiology, 2006

Ecdysteroid titers and expression profiles of ecdysone-regulated genes were determined during the last instar larval and during the pupal stages of Aedes aegypti (Diptera: Culicidae). Three peaks of ecdysteroids occurring at approximately 24, 30-33 and 45-48 h after ecdysis to the fourth instar larval stage were detected. In the pupa, a large peak of ecdysteroids occurred between 6 and 12 h after ecdysis to the pupal stage. A small rise in ecdysteroids was also detected at the end of the pupal stage. Quantitative reverse transcriptase polymerase chain reaction analyses of the expression of ecdysone receptors and ecdysone-regulated genes showed that the peaks of expression of most of these genes coincided with the rise in ecdysteroid levels during the last larval and pupal stages. In the last larval stage, ecdysteroid titers and mRNA expression profiles of ecdysone-regulated genes are similar to those observed for Drosophila melanogaster. However, in the early pupal stage, both ecdysteroid titers and the expression of ecdysone-regulated genes are somewhat different from those observed in D. melanogaster, probably because the duration of the pupal stage in D. melanogaster is 84 h while in Ae. aeqypti the duration is only 48 h. These data which describe the relationship between ecdysteroid titers and mRNA levels of Ae. aegypti ecdysteroid-regulated genes lay a solid foundation for future studies on the hormonal regulation of development in mosquitoes.

The vitellogenin gene of the mosquito Aedes aegypti is a direct target of ecdysteroid receptor

Molecular and Cellular Endocrinology, 2001

In the female mosquito Aedes aegypti, vitellogenin (Vg), the major YPP, is activated by 20-hydroxyecdysone (20E) at the transcriptional level. We used cell transfection assays in the Drosophila S2 cells to investigate whether 20E acts directly on the Vg gene via its functional receptor, the heterodimer composed of the ecdysteroid receptor (EcR) and the ultraspiracle (USP) proteins. We demonstrated that the Vg 5%-regulatory region contains a functional ecdysteroid-responsive element (VgEcRE1) that is necessary to confer responsiveness to 20E. VgEcRE binds directly to EcR-USP produced in vitro and extracted from the vitellogenic fat body nuclei. The binding intensity of the EcR-USP-EcRE1 complex from nuclear extracts corresponds to the levels of ecdysteroids and of the Vg transcript during the vitellogenic cycle. Given the modest level of 20E-dependent activation, it is likely that the EcR-USP receptor acts synergistically with other transcription factors to bring about the high level of Vg gene expression.

Conservation of ecdysis-triggering hormone signalling in insects

Journal of Experimental Biology, 2003

SUMMARYPre-ecdysis- and ecdysis-triggering hormones (PETH and ETH) from endocrine Inka cells initiate ecdysis in moths and Drosophila through direct actions on the central nervous system (CNS). Using immunohistochemistry, we found Inka cells in representatives of all major insect orders. In most insects, Inka cells are numerous, small and scattered throughout the tracheal system. Only some higher holometabolous insects exhibit 8-9 pairs of large Inka cells attached to tracheae in each prothoracic and abdominal segment. The number and morphology of Inka cells can be very variable even in the same individuals or related insects, but all produce peptide hormones that are completely released at each ecdysis. Injection of tracheal extracts prepared from representatives of several insect orders induces pre-ecdysis and ecdysis behaviours in pharate larvae of Bombyx, indicating functional similarity of these peptides. We isolated several PETH-immunoreactive peptides from tracheal extracts o...

Evidence for expression of EcR and USP components of the 20-hydroxyecdysone receptor by a mosquito cell line

Archives of Insect Biochemistry and Physiology, 2000

The reverse transcriptase polymerase chain reaction (RT-PCR) was used to examine whether the C7-10 cell line from the mosquito, Aedes albopictus, expresses transcripts encoding 20hydroxyecdysone receptor (EcR) and ultraspiracle (USP) isoforms known to constitute a functional 20-hydroxyecdysone receptor. Here we describe recovery and analysis of products with high similarity to the EcR and to the USP isoform "a" that have been reported from the related mosquito, Aedes aegypti. The C7-10 EcR was 97% identical to Aedes aegypti EcR in amino acid sequence. Key features of the nuclear/steroid hormone receptor superfamily, including the zinc fingers, proximal (P)-box, and distal (D)-box were well conserved. However, the C7-10 EcR contained 5 additional amino acids in the Cterminal domain F, which required introduction of gaps to maximize alignment. The 5¢-untranslated regions of the two mosquito EcRs were 98% identical, but the function of this region remains unknown. The C7-10 USP was 95% identical in amino acid sequence to the longer Aedes aegypti isoform "a." Although only the C7-10 EcR was detected on Northern blots using total RNA from the cell line, transcripts for both EcR and USP were detected using the RT-PCR procedure. These transcripts appeared to be expressed constitutively and expression levels were not affected by treatment of cells with 20hydroxyecdysone. Arch. Insect Biochem. Physiol. 43:87-96, 2000.

Juvenile hormone-regulated alternative splicing of thetaimangene primes the ecdysteroid response in adult mosquitoes

Proceedings of the National Academy of Sciences, 2018

SignificanceMany physiological events in insects are controlled by both juvenile hormone (JH) and 20-hydroxyecdysone (20E). The presence of JH sometimes alters the nature of the 20E action, but the underlying mechanisms have not been fully elucidated. InAedes aegyptimosquitoes, four protein isoforms are generated by thetaimangene, which plays an indispensable role in the action of both JH and 20E. Our study indicates that different hormone responses demand distinct Taiman isoforms. Moreover, JH controls the formation of the Taiman isoforms that are specifically required for 20E-regulated gene expression after blood feeding. Therefore, this study discovers a previously unknown mode of JH action and provides insight into how JH influences cellular responses to 20E in insects.

Conserved Molecular Mechanism for the Stage Specificity of the Mosquito Vitellogenic Response to Ecdysone

Developmental Biology, 2000

In the mosquito Aedes aegypti, the adult female becomes competent for a vitellogenic response to ecdysone after previtellogenic development. Here, we show that ␤FTZ-F1, the nuclear receptor implicated as a competence factor for stage-specific responses to ecdysone during Drosophila metamorphosis, serves a similar function during mosquito vitellogenesis. AaFTZ-F1 is expressed highly in the mosquito fat body during pre-and postvitellogenic periods when ecdysteroid titers are low. The mosquito AaFTZ-F1 transcript nearly disappears in mid-vitellogenesis when ecdysteroid titers are high. An expression peak of HR3, a nuclear receptor implicated in the activation of ␤FTZ-F1 in Drosophila, precedes each rise in mosquito FTZ-F1 expression. In in vitro fat body culture, AaFTZ-F1 expression is inhibited by 20-hydroxyecdysone (20E) and superactivated by its withdrawal. Following in vitro AaFTZ-F1 superactivation, a secondary 20E challenge results in superinduction of the early AaE75 gene and the late target VCP gene. Electrophoretic mobility-shift assays show that the onset of ecdysone-response competence in the mosquito fat body is correlated with the appearance of the functional AaFTZ-F1 protein at the end of the previtellogenic development. These findings suggest that a conserved molecular mechanism for controlling stage specificity is reiteratively used during metamorphic and reproductive responses to ecdysone.

Molecular identification of the first insect ecdysis triggering hormone receptors

Biochemical and Biophysical Research Communications, 2002

The Drosophila Genome Project website (www.flybase.org) contains an annotated gene sequence (CG5911), coding for a G protein-coupled receptor. We cloned the cDNA corresponding to this sequence and found that the gene has not been correctly predicted. The corrected gene CG5911 has five introns and six exons (1-6). Alternative splicing yields two cDNAs called A (containing exons 1-5) and B (containing exons 1-4, 6). We expressed these splicing variants in Chinese hamster ovary cells and found that the corrected CG5911-A and -B cDNAs coded for two different G protein-coupled receptors that could be activated by low concentrations of Drosophila ecdysis triggering hormones-1 and -2. Ecdysis (cuticle shedding) is an important behaviour, allowing growth and metamorphosis in insects and other arthropods. Our paper is the first report on the molecular identification of ecdysis triggering hormone receptors from insects.

The early gene Broad is involved in the ecdysteroid hierarchy governing vitellogenesis of the mosquito Aedes aegypti

Journal of Molecular Endocrinology, 2004

The broad (br ) gene, encoding a family of C2H2 type zinc-finger DNA-binding proteins, has been shown to act as a crucial member of the 20-hydroxyecdysone (20E) regulatory hierarchy in the fruitfly, Drosophila melanogaster and the moth, Manduca sexta. In this study, we have shown that the br gene is involved in the 20E-regulatory hierarchy controlling vitellogenesis in the mosquito, Aedes aegypti. Unlike E74 and E75 early genes, expression of br was activated in previtellogenic females, during a juvenile hormone (JH)-dependent period. The levels of Z1, Z2 and Z4 isoform mRNA were elevated in the fat body of 2-day-old females after in vitro exposure to JH III. However, JH III repressed 20E activation of br in 3-to 5-day-old females, indicating a switch in hormonal commitment. Expression of Z1, Z2 and Z4 was stimulated after blood feeding in both vitellogenic tissues, the fat body and the ovary, corresponding to peaks of ecdysteroid titers. In the fat body, the mRNA profiles of these ...